{"database": "metadata", "table": "run_metadata", "is_view": false, "human_description_en": "where experiment.library_layout = \"SINGLE\", technology = \"bulk\" and tissue_curation_coarse = \"All anatomical structures\"", "rows": [[25273, "SRR25764091", "SRX21486763", "SRS18719063", "SRP457108", "PRJNA1009807", "Dynamics of the zebrafish tRNAome during the maternal to zygotic transition [RNA Seq]", "GSE241752", "Transcriptome Analysis", "Time course analysis of tRNA abundance during zebrafish early embryonic development. Overall design: Wild type TLAB strain zebrafish embryos were grown in standard housing conditions.Unfertilized eggs 0 hpf were collected or embryos were staged and collected at consecutive developmental time points  namelyat the 256 cell 2.5 hpf  1000 cell 3 hpf  sphere 4 hpf  shield 6 hpf and bud 10 hpf stages. Eggs and embryos were either flash frozen in liquid nitrogen or immediately processed. Samples were used for western blotting analysis  polysome profiling  ribosome profiling or mRNA and tRNA sequencing for investigating the regulation of tRNA gene expression and translational status during early zebrafish embryogenesis.", "parent bioproject:PRJNA1009800", "pubmed:39402326", null, "WT bud 10 hpf RNA seq rep2", "GSM7734768", null, "source name:Gastrula|strain:TLAB strain|tissue:Gastrula|developmental stage:Bud 10 hpf|genotype:WT|geo loc name:missing|collection date:missing", "WT bud 10 hpf RNA seq rep2", "3\u2019 adapters were trimmed using Trim Galore v0.6.4 with default settings  retaining reads of length \u226520. Reads were aligned to the GRCz11 zebrafish genome using STAR v2.6.1c with the following parameters:   outSAMtype BAM SortedByCoordinate   outFilterMultimapNmax 1   outFilterMismatchNmax 1   quantMode TranscriptomeSAM GeneCounts   alignEndsType Local   seedSearchStartLmax 14   alignIntronMax 10000   outFilterIntronMotifs RemoveNoncanonicalUnannotated. featureCounts v1.6.2 was used to count reads overlapping a filtered set of protein coding gene annotations from the GENCODE basic gene annotation. Differential gene expression analysis was performed using DESEq2 v1.38.1 with default settings and gene counts from featureCounts. Assembly: GRCz11 Supplementary files format and content: csv; transcripts per million TPM counts per transcript in MANE annotation", "Gastrula", "unperturbed growth conditions in E3 medium for zebrafish embryos.", "50 whole embryos were collected per sample and immediately lysed in 800uL LiDS/LET buffer5% Lithium dodecyl sulfate in 20 mM Tris HCl pH=7.4  100 mM LiCl  2 mM EDTA  5 mM DTT  pH 7.4. 250 ng of the same total RNA used for mim tRNAseq library preparation were used for mRNA Seq library construction with the Zymo Seq RiboFree Total RNA Library Kit Zymo Research  #R3000. Libraries were sequenced on a NextSeq 500 platform.", "Embryos were grown in standard housing conditions namely28\u00b0C at a 14/10 hour light/dark cycle.", "strain:TLAB strain|tissue:Gastrula|developmental stage:Bud 10 hpf|genotype:WT", "GSM7734768", "GSM7734768: WT bud 10 hpf RNA seq rep2; Danio rerio; RNA Seq", "GSM7734768 r1", "GSM7734768", "1", "50 whole embryos were collected per sample and immediately lysed in 800uL LiDS/LET buffer5% Lithium dodecyl sulfate in 20 mM Tris HCl pH=7.4  100 mM LiCl  2 mM EDTA  5 mM DTT  pH 7.4. 250 ng of the same total RNA used for mim tRNAseq library preparation were used for mRNA Seq library construction with the Zymo Seq RiboFree Total RNA Library Kit Zymo Research  #R3000. Libraries were sequenced on a NextSeq 500 platform.", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "NextSeq 500", null, "SRP457108", null, null, "WT_mRNA_bud_2.fastq.gz", "fastq", 2470912004.0, 31168086.0, "GSM7734768 r1", "0:79.28", "A:656817108;C:568241258;G:504262095;T:741507737;N:83806", 79, null, null, null, 656817108, 568241258, 504262095, 741507737, 83806, "SRX21486763", "SRS18719063", "SRA1700431", "Mechanisms of Protein Biogenesis, Max Planck Institute for Biochemistry", "Max Planck Institute of Biochemistry", 1, 0.91479, null, 0.27298, null, 0.74231, null, 0.57302, null, 79, null, "B", null, "usable mapping rate", "illumina", "nextseq", "unknown", "small_rna", "unknown", "bulk", "bulk", "bulk", null, "Germany", "2023-08-28", "Gastrula", "Embryo", "Whole Organism", "All anatomical structures"], [25274, "SRR25764092", "SRX21486762", "SRS18719064", "SRP457108", "PRJNA1009807", "Dynamics of the zebrafish tRNAome during the maternal to zygotic transition [RNA Seq]", "GSE241752", "Transcriptome Analysis", "Time course analysis of tRNA abundance during zebrafish early embryonic development. Overall design: Wild type TLAB strain zebrafish embryos were grown in standard housing conditions.Unfertilized eggs 0 hpf were collected or embryos were staged and collected at consecutive developmental time points  namelyat the 256 cell 2.5 hpf  1000 cell 3 hpf  sphere 4 hpf  shield 6 hpf and bud 10 hpf stages. Eggs and embryos were either flash frozen in liquid nitrogen or immediately processed. Samples were used for western blotting analysis  polysome profiling  ribosome profiling or mRNA and tRNA sequencing for investigating the regulation of tRNA gene expression and translational status during early zebrafish embryogenesis.", "parent bioproject:PRJNA1009800", "pubmed:39402326", null, "WT bud 10 hpf RNA seq rep1", "GSM7734767", null, "source name:Gastrula|strain:TLAB strain|tissue:Gastrula|developmental stage:Bud 10 hpf|genotype:WT|geo loc name:missing|collection date:missing", "WT bud 10 hpf RNA seq rep1", "3\u2019 adapters were trimmed using Trim Galore v0.6.4 with default settings  retaining reads of length \u226520. Reads were aligned to the GRCz11 zebrafish genome using STAR v2.6.1c with the following parameters:   outSAMtype BAM SortedByCoordinate   outFilterMultimapNmax 1   outFilterMismatchNmax 1   quantMode TranscriptomeSAM GeneCounts   alignEndsType Local   seedSearchStartLmax 14   alignIntronMax 10000   outFilterIntronMotifs RemoveNoncanonicalUnannotated. featureCounts v1.6.2 was used to count reads overlapping a filtered set of protein coding gene annotations from the GENCODE basic gene annotation. Differential gene expression analysis was performed using DESEq2 v1.38.1 with default settings and gene counts from featureCounts. Assembly: GRCz11 Supplementary files format and content: csv; transcripts per million TPM counts per transcript in MANE annotation", "Gastrula", "unperturbed growth conditions in E3 medium for zebrafish embryos.", "50 whole embryos were collected per sample and immediately lysed in 800uL LiDS/LET buffer5% Lithium dodecyl sulfate in 20 mM Tris HCl pH=7.4  100 mM LiCl  2 mM EDTA  5 mM DTT  pH 7.4. 250 ng of the same total RNA used for mim tRNAseq library preparation were used for mRNA Seq library construction with the Zymo Seq RiboFree Total RNA Library Kit Zymo Research  #R3000. Libraries were sequenced on a NextSeq 500 platform.", "Embryos were grown in standard housing conditions namely28\u00b0C at a 14/10 hour light/dark cycle.", "strain:TLAB strain|tissue:Gastrula|developmental stage:Bud 10 hpf|genotype:WT", "GSM7734767", "GSM7734767: WT bud 10 hpf RNA seq rep1; Danio rerio; RNA Seq", "GSM7734767 r1", "GSM7734767", "1", "50 whole embryos were collected per sample and immediately lysed in 800uL LiDS/LET buffer5% Lithium dodecyl sulfate in 20 mM Tris HCl pH=7.4  100 mM LiCl  2 mM EDTA  5 mM DTT  pH 7.4. 250 ng of the same total RNA used for mim tRNAseq library preparation were used for mRNA Seq library construction with the Zymo Seq RiboFree Total RNA Library Kit Zymo Research  #R3000. Libraries were sequenced on a NextSeq 500 platform.", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "NextSeq 500", null, "SRP457108", null, null, "WT_mRNA_bud_1.fastq.gz", "fastq", 2153494756.0, 27140032.0, "GSM7734767 r1", "0:79.35", "A:560793143;C:508962676;G:445126772;T:638539310;N:72855", 79, null, null, null, 560793143, 508962676, 445126772, 638539310, 72855, "SRX21486762", "SRS18719064", "SRA1700431", "Mechanisms of Protein Biogenesis, Max Planck Institute for Biochemistry", "Max Planck Institute of Biochemistry", 1, 0.88728, null, 0.25493, null, 0.74369, null, 0.56589, null, 80, null, "B", null, "usable mapping rate", "illumina", "nextseq", "unknown", "small_rna", "unknown", "bulk", "bulk", "bulk", null, "Germany", "2023-08-28", "Gastrula", "Embryo", "Whole Organism", "All anatomical structures"], [25275, "SRR25764093", "SRX21486761", "SRS18719061", "SRP457108", "PRJNA1009807", "Dynamics of the zebrafish tRNAome during the maternal to zygotic transition [RNA Seq]", "GSE241752", "Transcriptome Analysis", "Time course analysis of tRNA abundance during zebrafish early embryonic development. Overall design: Wild type TLAB strain zebrafish embryos were grown in standard housing conditions.Unfertilized eggs 0 hpf were collected or embryos were staged and collected at consecutive developmental time points  namelyat the 256 cell 2.5 hpf  1000 cell 3 hpf  sphere 4 hpf  shield 6 hpf and bud 10 hpf stages. Eggs and embryos were either flash frozen in liquid nitrogen or immediately processed. Samples were used for western blotting analysis  polysome profiling  ribosome profiling or mRNA and tRNA sequencing for investigating the regulation of tRNA gene expression and translational status during early zebrafish embryogenesis.", "parent bioproject:PRJNA1009800", "pubmed:39402326", null, "WT sphere 4 hpf RNA seq rep2", "GSM7734766", null, "source name:Blastula|strain:TLAB strain|tissue:Blastula|developmental stage:Sphere 4 hpf|genotype:WT|geo loc name:missing|collection date:missing", "WT sphere 4 hpf RNA seq rep2", "3\u2019 adapters were trimmed using Trim Galore v0.6.4 with default settings  retaining reads of length \u226520. Reads were aligned to the GRCz11 zebrafish genome using STAR v2.6.1c with the following parameters:   outSAMtype BAM SortedByCoordinate   outFilterMultimapNmax 1   outFilterMismatchNmax 1   quantMode TranscriptomeSAM GeneCounts   alignEndsType Local   seedSearchStartLmax 14   alignIntronMax 10000   outFilterIntronMotifs RemoveNoncanonicalUnannotated. featureCounts v1.6.2 was used to count reads overlapping a filtered set of protein coding gene annotations from the GENCODE basic gene annotation. Differential gene expression analysis was performed using DESEq2 v1.38.1 with default settings and gene counts from featureCounts. Assembly: GRCz11 Supplementary files format and content: csv; transcripts per million TPM counts per transcript in MANE annotation", "Blastula", "unperturbed growth conditions in E3 medium for zebrafish embryos.", "50 whole embryos were collected per sample and immediately lysed in 800uL LiDS/LET buffer5% Lithium dodecyl sulfate in 20 mM Tris HCl pH=7.4  100 mM LiCl  2 mM EDTA  5 mM DTT  pH 7.4. 250 ng of the same total RNA used for mim tRNAseq library preparation were used for mRNA Seq library construction with the Zymo Seq RiboFree Total RNA Library Kit Zymo Research  #R3000. Libraries were sequenced on a NextSeq 500 platform.", "Embryos were grown in standard housing conditions namely28\u00b0C at a 14/10 hour light/dark cycle.", "strain:TLAB strain|tissue:Blastula|developmental stage:Sphere 4 hpf|genotype:WT", "GSM7734766", "GSM7734766: WT sphere 4 hpf RNA seq rep2; Danio rerio; RNA Seq", "GSM7734766 r1", "GSM7734766", "1", "50 whole embryos were collected per sample and immediately lysed in 800uL LiDS/LET buffer5% Lithium dodecyl sulfate in 20 mM Tris HCl pH=7.4  100 mM LiCl  2 mM EDTA  5 mM DTT  pH 7.4. 250 ng of the same total RNA used for mim tRNAseq library preparation were used for mRNA Seq library construction with the Zymo Seq RiboFree Total RNA Library Kit Zymo Research  #R3000. Libraries were sequenced on a NextSeq 500 platform.", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "NextSeq 500", null, "SRP457108", null, null, "WT_mRNA_sphere_2.fastq.gz", "fastq", 2455317157.0, 30934591.0, "GSM7734766 r1", "0:79.37", "A:614860604;C:588586084;G:522132289;T:729655621;N:82559", 79, null, null, null, 614860604, 588586084, 522132289, 729655621, 82559, "SRX21486761", "SRS18719061", "SRA1700431", "Mechanisms of Protein Biogenesis, Max Planck Institute for Biochemistry", "Max Planck Institute of Biochemistry", 1, 0.94124, null, 0.10502, null, 0.74876, null, 0.57752, null, 80, null, "B", null, "usable mapping rate", "illumina", "nextseq", "unknown", "small_rna", "unknown", "bulk", "bulk", "bulk", null, "Germany", "2023-08-28", "Blastula", "Embryo", "Whole Organism", "All anatomical structures"], [25276, "SRR25764094", "SRX21486760", "SRS18719060", "SRP457108", "PRJNA1009807", "Dynamics of the zebrafish tRNAome during the maternal to zygotic transition [RNA Seq]", "GSE241752", "Transcriptome Analysis", "Time course analysis of tRNA abundance during zebrafish early embryonic development. Overall design: Wild type TLAB strain zebrafish embryos were grown in standard housing conditions.Unfertilized eggs 0 hpf were collected or embryos were staged and collected at consecutive developmental time points  namelyat the 256 cell 2.5 hpf  1000 cell 3 hpf  sphere 4 hpf  shield 6 hpf and bud 10 hpf stages. Eggs and embryos were either flash frozen in liquid nitrogen or immediately processed. Samples were used for western blotting analysis  polysome profiling  ribosome profiling or mRNA and tRNA sequencing for investigating the regulation of tRNA gene expression and translational status during early zebrafish embryogenesis.", "parent bioproject:PRJNA1009800", "pubmed:39402326", null, "WT sphere 4 hpf RNA seq rep1", "GSM7734765", null, "source name:Blastula|strain:TLAB strain|tissue:Blastula|developmental stage:Sphere 4 hpf|genotype:WT|geo loc name:missing|collection date:missing", "WT sphere 4 hpf RNA seq rep1", "3\u2019 adapters were trimmed using Trim Galore v0.6.4 with default settings  retaining reads of length \u226520. Reads were aligned to the GRCz11 zebrafish genome using STAR v2.6.1c with the following parameters:   outSAMtype BAM SortedByCoordinate   outFilterMultimapNmax 1   outFilterMismatchNmax 1   quantMode TranscriptomeSAM GeneCounts   alignEndsType Local   seedSearchStartLmax 14   alignIntronMax 10000   outFilterIntronMotifs RemoveNoncanonicalUnannotated. featureCounts v1.6.2 was used to count reads overlapping a filtered set of protein coding gene annotations from the GENCODE basic gene annotation. Differential gene expression analysis was performed using DESEq2 v1.38.1 with default settings and gene counts from featureCounts. Assembly: GRCz11 Supplementary files format and content: csv; transcripts per million TPM counts per transcript in MANE annotation", "Blastula", "unperturbed growth conditions in E3 medium for zebrafish embryos.", "50 whole embryos were collected per sample and immediately lysed in 800uL LiDS/LET buffer5% Lithium dodecyl sulfate in 20 mM Tris HCl pH=7.4  100 mM LiCl  2 mM EDTA  5 mM DTT  pH 7.4. 250 ng of the same total RNA used for mim tRNAseq library preparation were used for mRNA Seq library construction with the Zymo Seq RiboFree Total RNA Library Kit Zymo Research  #R3000. Libraries were sequenced on a NextSeq 500 platform.", "Embryos were grown in standard housing conditions namely28\u00b0C at a 14/10 hour light/dark cycle.", "strain:TLAB strain|tissue:Blastula|developmental stage:Sphere 4 hpf|genotype:WT", "GSM7734765", "GSM7734765: WT sphere 4 hpf RNA seq rep1; Danio rerio; RNA Seq", "GSM7734765 r1", "GSM7734765", "1", "50 whole embryos were collected per sample and immediately lysed in 800uL LiDS/LET buffer5% Lithium dodecyl sulfate in 20 mM Tris HCl pH=7.4  100 mM LiCl  2 mM EDTA  5 mM DTT  pH 7.4. 250 ng of the same total RNA used for mim tRNAseq library preparation were used for mRNA Seq library construction with the Zymo Seq RiboFree Total RNA Library Kit Zymo Research  #R3000. Libraries were sequenced on a NextSeq 500 platform.", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "NextSeq 500", null, "SRP457108", null, null, "WT_mRNA_sphere_1.fastq.gz", "fastq", 2399640874.0, 30232118.0, "GSM7734765 r1", "0:79.37", "A:589069860;C:593745131;G:511439690;T:705305674;N:80519", 79, null, null, null, 589069860, 593745131, 511439690, 705305674, 80519, "SRX21486760", "SRS18719060", "SRA1700431", "Mechanisms of Protein Biogenesis, Max Planck Institute for Biochemistry", "Max Planck Institute of Biochemistry", 1, 0.85882, null, 0.11848, null, 0.75122, null, 0.5883, null, 80, null, "B", null, "usable mapping rate", "illumina", "nextseq", "unknown", "small_rna", "unknown", "bulk", "bulk", "bulk", null, "Germany", "2023-08-28", "Blastula", "Embryo", "Whole Organism", "All anatomical structures"], [28113, "SRR26209648", "SRX21920662", "SRS19005181", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 WT 3", "GSM7812991", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:WT|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 WT 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:WT|treatment:unDMSO", "GSM7812991", "GSM7812991: unDMSO t1 WT 3; Danio rerio; RNA Seq", "GSM7812991 r1", "GSM7812991", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A30_S48_L005_R1_001.fastq.gz", "fastq", 616449359.0, 6103459.0, "GSM7812991 r1", "0:101", "A:152808626;C:149738763;G:141639387;T:172257280;N:5303", 101, null, null, null, 152808626, 149738763, 141639387, 172257280, 5303, "SRX21920662", "SRS19005181", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94246, null, 0.08766, null, 0.69443, null, 0.4842, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28114, "SRR26209649", "SRX21920662", "SRS19005181", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 WT 3", "GSM7812991", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:WT|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 WT 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:WT|treatment:unDMSO", "GSM7812991", "GSM7812991: unDMSO t1 WT 3; Danio rerio; RNA Seq", "GSM7812991 r1", "GSM7812991", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A30_S48_L006_R1_001.fastq.gz", "fastq", 609999297.0, 6039597.0, "GSM7812991 r2", "0:101", "A:151226657;C:148143193;G:140088806;T:170530812;N:9829", 101, null, null, null, 151226657, 148143193, 140088806, 170530812, 9829, "SRX21920662", "SRS19005181", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94201, null, 0.08569, null, 0.69572, null, 0.48692, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28115, "SRR26209650", "SRX21920662", "SRS19005181", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 WT 3", "GSM7812991", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:WT|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 WT 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:WT|treatment:unDMSO", "GSM7812991", "GSM7812991: unDMSO t1 WT 3; Danio rerio; RNA Seq", "GSM7812991 r1", "GSM7812991", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A30_S48_L007_R1_001.fastq.gz", "fastq", 543730470.0, 5383470.0, "GSM7812991 r3", "0:101", "A:134685766;C:132190291;G:124881864;T:151967639;N:4910", 101, null, null, null, 134685766, 132190291, 124881864, 151967639, 4910, "SRX21920662", "SRS19005181", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.9431, null, 0.08733, null, 0.69524, null, 0.48528, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28116, "SRR26209651", "SRX21920662", "SRS19005181", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 WT 3", "GSM7812991", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:WT|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 WT 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:WT|treatment:unDMSO", "GSM7812991", "GSM7812991: unDMSO t1 WT 3; Danio rerio; RNA Seq", "GSM7812991 r1", "GSM7812991", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A30_S16_L007_R1_001.fastq.gz", "fastq", 649354149.0, 6429249.0, "GSM7812991 r4", "0:101", "A:160756303;C:158145998;G:149623680;T:180816390;N:11778", 101, null, null, null, 160756303, 158145998, 149623680, 180816390, 11778, "SRX21920662", "SRS19005181", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94438, null, 0.08618, null, 0.69473, null, 0.48809, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28117, "SRR26209752", "SRX21920662", "SRS19005181", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 WT 3", "GSM7812991", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:WT|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 WT 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:WT|treatment:unDMSO", "GSM7812991", "GSM7812991: unDMSO t1 WT 3; Danio rerio; RNA Seq", "GSM7812991 r1", "GSM7812991", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A30_S16_L008_R1_001.fastq.gz", "fastq", 650450504.0, 6440104.0, "GSM7812991 r5", "0:101", "A:161054597;C:158340761;G:149784923;T:181251361;N:18862", 101, null, null, null, 161054597, 158340761, 149784923, 181251361, 18862, "SRX21920662", "SRS19005181", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94338, null, 0.08713, null, 0.6968, null, 0.48443, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28118, "SRR26209652", "SRX21920661", "SRS19005180", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 WT 2", "GSM7812990", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:WT|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 WT 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:WT|treatment:unDMSO", "GSM7812990", "GSM7812990: unDMSO t1 WT 2; Danio rerio; RNA Seq", "GSM7812990 r1", "GSM7812990", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A29_S46_L005_R1_001.fastq.gz", "fastq", 593068162.0, 5871962.0, "GSM7812990 r1", "0:101", "A:147906639;C:143944406;G:137307101;T:163904929;N:5087", 101, null, null, null, 147906639, 143944406, 137307101, 163904929, 5087, "SRX21920661", "SRS19005180", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94371, null, 0.06473, null, 0.69378, null, 0.47765, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28119, "SRR26209653", "SRX21920661", "SRS19005180", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 WT 2", "GSM7812990", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:WT|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 WT 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:WT|treatment:unDMSO", "GSM7812990", "GSM7812990: unDMSO t1 WT 2; Danio rerio; RNA Seq", "GSM7812990 r1", "GSM7812990", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A29_S46_L006_R1_001.fastq.gz", "fastq", 588323081.0, 5824981.0, "GSM7812990 r2", "0:101", "A:146630863;C:142829925;G:136124185;T:162728186;N:9922", 101, null, null, null, 146630863, 142829925, 136124185, 162728186, 9922, "SRX21920661", "SRS19005180", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94282, null, 0.06357, null, 0.69418, null, 0.47665, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28120, "SRR26209654", "SRX21920661", "SRS19005180", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 WT 2", "GSM7812990", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:WT|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 WT 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:WT|treatment:unDMSO", "GSM7812990", "GSM7812990: unDMSO t1 WT 2; Danio rerio; RNA Seq", "GSM7812990 r1", "GSM7812990", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A29_S46_L007_R1_001.fastq.gz", "fastq", 521265747.0, 5161047.0, "GSM7812990 r3", "0:101", "A:129905878;C:126622019;G:120526207;T:144206853;N:4790", 101, null, null, null, 129905878, 126622019, 120526207, 144206853, 4790, "SRX21920661", "SRS19005180", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94508, null, 0.06499, null, 0.69367, null, 0.4834, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28121, "SRR26209655", "SRX21920661", "SRS19005180", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 WT 2", "GSM7812990", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:WT|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 WT 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:WT|treatment:unDMSO", "GSM7812990", "GSM7812990: unDMSO t1 WT 2; Danio rerio; RNA Seq", "GSM7812990 r1", "GSM7812990", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A29_S26_L007_R1_001.fastq.gz", "fastq", 623834580.0, 6176580.0, "GSM7812990 r4", "0:101", "A:155642981;C:151651242;G:144681951;T:171847192;N:11214", 101, null, null, null, 155642981, 151651242, 144681951, 171847192, 11214, "SRX21920661", "SRS19005180", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94531, null, 0.06514, null, 0.69225, null, 0.48187, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28122, "SRR26209656", "SRX21920661", "SRS19005180", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 WT 2", "GSM7812990", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:WT|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 WT 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:WT|treatment:unDMSO", "GSM7812990", "GSM7812990: unDMSO t1 WT 2; Danio rerio; RNA Seq", "GSM7812990 r1", "GSM7812990", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A29_S26_L008_R1_001.fastq.gz", "fastq", 622155960.0, 6159960.0, "GSM7812990 r5", "0:101", "A:155145221;C:151231599;G:144290581;T:171470641;N:17918", 101, null, null, null, 155145221, 151231599, 144290581, 171470641, 17918, "SRX21920661", "SRS19005180", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94319, null, 0.06413, null, 0.69449, null, 0.48159, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28123, "SRR26209657", "SRX21920660", "SRS19005179", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 WT 1", "GSM7812989", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:WT|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 WT 1", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:WT|treatment:unDMSO", "GSM7812989", "GSM7812989: unDMSO t1 WT 1; Danio rerio; RNA Seq", "GSM7812989 r1", "GSM7812989", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A28_S45_L005_R1_001.fastq.gz", "fastq", 602520550.0, 5965550.0, "GSM7812989 r1", "0:101", "A:149619230;C:146559346;G:139674646;T:166662143;N:5185", 101, null, null, null, 149619230, 146559346, 139674646, 166662143, 5185, "SRX21920660", "SRS19005179", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94449, null, 0.06296, null, 0.69487, null, 0.48, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28124, "SRR26209658", "SRX21920660", "SRS19005179", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 WT 1", "GSM7812989", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:WT|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 WT 1", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:WT|treatment:unDMSO", "GSM7812989", "GSM7812989: unDMSO t1 WT 1; Danio rerio; RNA Seq", "GSM7812989 r1", "GSM7812989", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A28_S45_L006_R1_001.fastq.gz", "fastq", 596942522.0, 5910322.0, "GSM7812989 r2", "0:101", "A:148193962;C:145221539;G:138267073;T:165249833;N:10115", 101, null, null, null, 148193962, 145221539, 138267073, 165249833, 10115, "SRX21920660", "SRS19005179", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.9446, null, 0.06327, null, 0.69562, null, 0.48183, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28125, "SRR26209659", "SRX21920660", "SRS19005179", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 WT 1", "GSM7812989", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:WT|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 WT 1", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:WT|treatment:unDMSO", "GSM7812989", "GSM7812989: unDMSO t1 WT 1; Danio rerio; RNA Seq", "GSM7812989 r1", "GSM7812989", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A28_S45_L007_R1_001.fastq.gz", "fastq", 532539064.0, 5272664.0, "GSM7812989 r3", "0:101", "A:132217323;C:129660296;G:123303893;T:147352732;N:4820", 101, null, null, null, 132217323, 129660296, 123303893, 147352732, 4820, "SRX21920660", "SRS19005179", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94579, null, 0.06237, null, 0.69554, null, 0.46658, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28126, "SRR26209660", "SRX21920660", "SRS19005179", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 WT 1", "GSM7812989", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:WT|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 WT 1", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:WT|treatment:unDMSO", "GSM7812989", "GSM7812989: unDMSO t1 WT 1; Danio rerio; RNA Seq", "GSM7812989 r1", "GSM7812989", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A28_S29_L007_R1_001.fastq.gz", "fastq", 633337569.0, 6270669.0, "GSM7812989 r4", "0:101", "A:157286526;C:154336036;G:147137950;T:174565295;N:11762", 101, null, null, null, 157286526, 154336036, 147137950, 174565295, 11762, "SRX21920660", "SRS19005179", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94562, null, 0.06294, null, 0.69489, null, 0.47406, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28127, "SRR26209661", "SRX21920660", "SRS19005179", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 WT 1", "GSM7812989", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:WT|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 WT 1", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:WT|treatment:unDMSO", "GSM7812989", "GSM7812989: unDMSO t1 WT 1; Danio rerio; RNA Seq", "GSM7812989 r1", "GSM7812989", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A28_S29_L008_R1_001.fastq.gz", "fastq", 636051540.0, 6297540.0, "GSM7812989 r5", "0:101", "A:157845668;C:154972063;G:147765532;T:175449801;N:18476", 101, null, null, null, 157845668, 154972063, 147765532, 175449801, 18476, "SRX21920660", "SRS19005179", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.9471, null, 0.06288, null, 0.69536, null, 0.4797, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28128, "SRR26209662", "SRX21920659", "SRS19005178", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 K2 3", "GSM7812988", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K2|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 K2 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K2|treatment:unDMSO", "GSM7812988", "GSM7812988: unDMSO t1 K2 3; Danio rerio; RNA Seq", "GSM7812988 r1", "GSM7812988", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A36_S54_L005_R1_001.fastq.gz", "fastq", 674188635.0, 6675135.0, "GSM7812988 r1", "0:101", "A:173104307;C:161481671;G:152542615;T:187053812;N:6230", 101, null, null, null, 173104307, 161481671, 152542615, 187053812, 6230, "SRX21920659", "SRS19005178", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94039, null, 0.07795, null, 0.69877, null, 0.48386, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28129, "SRR26209663", "SRX21920659", "SRS19005178", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 K2 3", "GSM7812988", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K2|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 K2 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K2|treatment:unDMSO", "GSM7812988", "GSM7812988: unDMSO t1 K2 3; Danio rerio; RNA Seq", "GSM7812988 r1", "GSM7812988", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A36_S54_L006_R1_001.fastq.gz", "fastq", 667048339.0, 6604439.0, "GSM7812988 r2", "0:101", "A:171316049;C:159786547;G:150743446;T:185190228;N:12069", 101, null, null, null, 171316049, 159786547, 150743446, 185190228, 12069, "SRX21920659", "SRS19005178", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94064, null, 0.07881, null, 0.69767, null, 0.48162, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28130, "SRR26209664", "SRX21920659", "SRS19005178", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 K2 3", "GSM7812988", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K2|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 K2 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K2|treatment:unDMSO", "GSM7812988", "GSM7812988: unDMSO t1 K2 3; Danio rerio; RNA Seq", "GSM7812988 r1", "GSM7812988", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A36_S54_L007_R1_001.fastq.gz", "fastq", 596645683.0, 5907383.0, "GSM7812988 r3", "0:101", "A:153131508;C:143126741;G:134745614;T:165635953;N:5867", 101, null, null, null, 153131508, 143126741, 134745614, 165635953, 5867, "SRX21920659", "SRS19005178", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94156, null, 0.07795, null, 0.69751, null, 0.4833, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28131, "SRR26209665", "SRX21920659", "SRS19005178", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 K2 3", "GSM7812988", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K2|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 K2 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K2|treatment:unDMSO", "GSM7812988", "GSM7812988: unDMSO t1 K2 3; Danio rerio; RNA Seq", "GSM7812988 r1", "GSM7812988", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A36_S12_L007_R1_001.fastq.gz", "fastq", 712385926.0, 7053326.0, "GSM7812988 r4", "0:101", "A:183100436;C:171026605;G:161510527;T:196734608;N:13750", 101, null, null, null, 183100436, 171026605, 161510527, 196734608, 13750, "SRX21920659", "SRS19005178", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94298, null, 0.07892, null, 0.6997, null, 0.48331, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28132, "SRR26209666", "SRX21920659", "SRS19005178", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 K2 3", "GSM7812988", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K2|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 K2 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K2|treatment:unDMSO", "GSM7812988", "GSM7812988: unDMSO t1 K2 3; Danio rerio; RNA Seq", "GSM7812988 r1", "GSM7812988", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A36_S12_L008_R1_001.fastq.gz", "fastq", 714661355.0, 7075855.0, "GSM7812988 r5", "0:101", "A:183454698;C:171554090;G:162064705;T:197567065;N:20797", 101, null, null, null, 183454698, 171554090, 162064705, 197567065, 20797, "SRX21920659", "SRS19005178", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94316, null, 0.07877, null, 0.70051, null, 0.48354, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28133, "SRR26209667", "SRX21920658", "SRS19005177", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 K2 2", "GSM7812987", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K2|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 K2 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K2|treatment:unDMSO", "GSM7812987", "GSM7812987: unDMSO t1 K2 2; Danio rerio; RNA Seq", "GSM7812987 r1", "GSM7812987", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A35_S53_L005_R1_001.fastq.gz", "fastq", 611900723.0, 6058423.0, "GSM7812987 r1", "0:101", "A:154668392;C:147817141;G:139653400;T:169756342;N:5448", 101, null, null, null, 154668392, 147817141, 139653400, 169756342, 5448, "SRX21920658", "SRS19005177", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94636, null, 0.08022, null, 0.69962, null, 0.48201, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28134, "SRR26209668", "SRX21920658", "SRS19005177", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 K2 2", "GSM7812987", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K2|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 K2 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K2|treatment:unDMSO", "GSM7812987", "GSM7812987: unDMSO t1 K2 2; Danio rerio; RNA Seq", "GSM7812987 r1", "GSM7812987", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A35_S53_L006_R1_001.fastq.gz", "fastq", 602971818.0, 5970018.0, "GSM7812987 r2", "0:101", "A:152346877;C:145640105;G:137576284;T:167398281;N:10271", 101, null, null, null, 152346877, 145640105, 137576284, 167398281, 10271, "SRX21920658", "SRS19005177", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94549, null, 0.08086, null, 0.69781, null, 0.47842, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28135, "SRR26209669", "SRX21920658", "SRS19005177", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 K2 2", "GSM7812987", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K2|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 K2 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K2|treatment:unDMSO", "GSM7812987", "GSM7812987: unDMSO t1 K2 2; Danio rerio; RNA Seq", "GSM7812987 r1", "GSM7812987", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A35_S53_L007_R1_001.fastq.gz", "fastq", 539246575.0, 5339075.0, "GSM7812987 r3", "0:101", "A:136317506;C:130390122;G:122927887;T:149606028;N:5032", 101, null, null, null, 136317506, 130390122, 122927887, 149606028, 5032, "SRX21920658", "SRS19005177", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94653, null, 0.08075, null, 0.69704, null, 0.48374, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28136, "SRR26209670", "SRX21920658", "SRS19005177", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 K2 2", "GSM7812987", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K2|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 K2 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K2|treatment:unDMSO", "GSM7812987", "GSM7812987: unDMSO t1 K2 2; Danio rerio; RNA Seq", "GSM7812987 r1", "GSM7812987", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A35_S47_L007_R1_001.fastq.gz", "fastq", 643197593.0, 6368293.0, "GSM7812987 r4", "0:101", "A:162743675;C:155711536;G:147135700;T:177594459;N:12223", 101, null, null, null, 162743675, 155711536, 147135700, 177594459, 12223, "SRX21920658", "SRS19005177", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94757, null, 0.08023, null, 0.70055, null, 0.48458, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28137, "SRR26209671", "SRX21920658", "SRS19005177", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 K2 2", "GSM7812987", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K2|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 K2 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K2|treatment:unDMSO", "GSM7812987", "GSM7812987: unDMSO t1 K2 2; Danio rerio; RNA Seq", "GSM7812987 r1", "GSM7812987", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A35_S47_L008_R1_001.fastq.gz", "fastq", 644356063.0, 6379763.0, "GSM7812987 r5", "0:101", "A:162915651;C:155935181;G:147406641;T:178079118;N:19472", 101, null, null, null, 162915651, 155935181, 147406641, 178079118, 19472, "SRX21920658", "SRS19005177", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94817, null, 0.08218, null, 0.70017, null, 0.48286, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28138, "SRR26209672", "SRX21920657", "SRS19005176", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 K2 1", "GSM7812986", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K2|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 K2 1", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K2|treatment:unDMSO", "GSM7812986", "GSM7812986: unDMSO t1 K2 1; Danio rerio; RNA Seq", "GSM7812986 r1", "GSM7812986", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A34_S52_L005_R1_001.fastq.gz", "fastq", 615996374.0, 6098974.0, "GSM7812986 r1", "0:101", "A:156934542;C:147417998;G:139301915;T:172336421;N:5498", 101, null, null, null, 156934542, 147417998, 139301915, 172336421, 5498, "SRX21920657", "SRS19005176", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94179, null, 0.07628, null, 0.69512, null, 0.48041, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28139, "SRR26209673", "SRX21920657", "SRS19005176", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 K2 1", "GSM7812986", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K2|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 K2 1", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K2|treatment:unDMSO", "GSM7812986", "GSM7812986: unDMSO t1 K2 1; Danio rerio; RNA Seq", "GSM7812986 r1", "GSM7812986", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A34_S52_L006_R1_001.fastq.gz", "fastq", 608875571.0, 6028471.0, "GSM7812986 r2", "0:101", "A:155127967;C:145701864;G:137575885;T:170459017;N:10838", 101, null, null, null, 155127967, 145701864, 137575885, 170459017, 10838, "SRX21920657", "SRS19005176", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94248, null, 0.07563, null, 0.69512, null, 0.47982, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28140, "SRR26209674", "SRX21920657", "SRS19005176", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 K2 1", "GSM7812986", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K2|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 K2 1", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K2|treatment:unDMSO", "GSM7812986", "GSM7812986: unDMSO t1 K2 1; Danio rerio; RNA Seq", "GSM7812986 r1", "GSM7812986", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A34_S52_L007_R1_001.fastq.gz", "fastq", 539739455.0, 5343955.0, "GSM7812986 r3", "0:101", "A:137431217;C:129328124;G:121891472;T:151083373;N:5269", 101, null, null, null, 137431217, 129328124, 121891472, 151083373, 5269, "SRX21920657", "SRS19005176", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.9438, null, 0.07511, null, 0.69654, null, 0.48083, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28141, "SRR26209675", "SRX21920657", "SRS19005176", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 K2 1", "GSM7812986", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K2|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 K2 1", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K2|treatment:unDMSO", "GSM7812986", "GSM7812986: unDMSO t1 K2 1; Danio rerio; RNA Seq", "GSM7812986 r1", "GSM7812986", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A34_S65_L007_R1_001.fastq.gz", "fastq", 648984489.0, 6425589.0, "GSM7812986 r4", "0:101", "A:165552674;C:155580501;G:147078092;T:180761105;N:12117", 101, null, null, null, 165552674, 155580501, 147078092, 180761105, 12117, "SRX21920657", "SRS19005176", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94513, null, 0.07694, null, 0.69451, null, 0.48174, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28142, "SRR26209676", "SRX21920657", "SRS19005176", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 K2 1", "GSM7812986", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K2|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 K2 1", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K2|treatment:unDMSO", "GSM7812986", "GSM7812986: unDMSO t1 K2 1; Danio rerio; RNA Seq", "GSM7812986 r1", "GSM7812986", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A34_S65_L008_R1_001.fastq.gz", "fastq", 651988330.0, 6455330.0, "GSM7812986 r5", "0:101", "A:166130853;C:156282200;G:147738788;T:181817695;N:18794", 101, null, null, null, 166130853, 156282200, 147738788, 181817695, 18794, "SRX21920657", "SRS19005176", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94437, null, 0.0759, null, 0.69597, null, 0.48083, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28143, "SRR26209677", "SRX21920656", "SRS19005175", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 K1 3", "GSM7812985", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K1|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 K1 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K1|treatment:unDMSO", "GSM7812985", "GSM7812985: unDMSO t1 K1 3; Danio rerio; RNA Seq", "GSM7812985 r1", "GSM7812985", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A33_S51_L005_R1_001.fastq.gz", "fastq", 621669544.0, 6155144.0, "GSM7812985 r1", "0:101", "A:157346917;C:148083763;G:141122336;T:175110946;N:5582", 101, null, null, null, 157346917, 148083763, 141122336, 175110946, 5582, "SRX21920656", "SRS19005175", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94207, null, 0.06859, null, 0.69473, null, 0.48838, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28144, "SRR26209678", "SRX21920656", "SRS19005175", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 K1 3", "GSM7812985", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K1|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 K1 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K1|treatment:unDMSO", "GSM7812985", "GSM7812985: unDMSO t1 K1 3; Danio rerio; RNA Seq", "GSM7812985 r1", "GSM7812985", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A33_S51_L006_R1_001.fastq.gz", "fastq", 613437842.0, 6073642.0, "GSM7812985 r2", "0:101", "A:155200714;C:146135271;G:139223090;T:172868018;N:10749", 101, null, null, null, 155200714, 146135271, 139223090, 172868018, 10749, "SRX21920656", "SRS19005175", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94144, null, 0.06885, null, 0.69471, null, 0.48996, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28145, "SRR26209679", "SRX21920656", "SRS19005175", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 K1 3", "GSM7812985", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K1|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 K1 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K1|treatment:unDMSO", "GSM7812985", "GSM7812985: unDMSO t1 K1 3; Danio rerio; RNA Seq", "GSM7812985 r1", "GSM7812985", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A33_S51_L007_R1_001.fastq.gz", "fastq", 546684518.0, 5412718.0, "GSM7812985 r3", "0:101", "A:138292090;C:130364936;G:123978492;T:154043685;N:5315", 101, null, null, null, 138292090, 130364936, 123978492, 154043685, 5315, "SRX21920656", "SRS19005175", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94375, null, 0.06988, null, 0.69589, null, 0.48741, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28146, "SRR26209680", "SRX21920656", "SRS19005175", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 K1 3", "GSM7812985", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K1|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 K1 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K1|treatment:unDMSO", "GSM7812985", "GSM7812985: unDMSO t1 K1 3; Danio rerio; RNA Seq", "GSM7812985 r1", "GSM7812985", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A33_S43_L007_R1_001.fastq.gz", "fastq", 651065089.0, 6446189.0, "GSM7812985 r4", "0:101", "A:164874330;C:155389435;G:148130531;T:182658473;N:12320", 101, null, null, null, 164874330, 155389435, 148130531, 182658473, 12320, "SRX21920656", "SRS19005175", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94247, null, 0.06954, null, 0.69538, null, 0.48283, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28147, "SRR26209681", "SRX21920656", "SRS19005175", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 K1 3", "GSM7812985", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K1|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 K1 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K1|treatment:unDMSO", "GSM7812985", "GSM7812985: unDMSO t1 K1 3; Danio rerio; RNA Seq", "GSM7812985 r1", "GSM7812985", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A33_S43_L008_R1_001.fastq.gz", "fastq", 652838952.0, 6463752.0, "GSM7812985 r5", "0:101", "A:165235507;C:155756581;G:148483290;T:183344035;N:19539", 101, null, null, null, 165235507, 155756581, 148483290, 183344035, 19539, "SRX21920656", "SRS19005175", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94297, null, 0.06917, null, 0.69593, null, 0.4827, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28148, "SRR26209682", "SRX21920655", "SRS19005174", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 K1 2", "GSM7812984", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K1|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 K1 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K1|treatment:unDMSO", "GSM7812984", "GSM7812984: unDMSO t1 K1 2; Danio rerio; RNA Seq", "GSM7812984 r1", "GSM7812984", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A32_S50_L005_R1_001.fastq.gz", "fastq", 531938215.0, 5266715.0, "GSM7812984 r1", "0:101", "A:131083905;C:128715617;G:122601298;T:149532970;N:4425", 101, null, null, null, 131083905, 128715617, 122601298, 149532970, 4425, "SRX21920655", "SRS19005174", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94249, null, 0.07108, null, 0.69485, null, 0.47386, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28149, "SRR26209683", "SRX21920655", "SRS19005174", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 K1 2", "GSM7812984", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K1|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 K1 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K1|treatment:unDMSO", "GSM7812984", "GSM7812984: unDMSO t1 K1 2; Danio rerio; RNA Seq", "GSM7812984 r1", "GSM7812984", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A32_S50_L006_R1_001.fastq.gz", "fastq", 527781863.0, 5225563.0, "GSM7812984 r2", "0:101", "A:130119726;C:127646784;G:121549831;T:148456993;N:8529", 101, null, null, null, 130119726, 127646784, 121549831, 148456993, 8529, "SRX21920655", "SRS19005174", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94199, null, 0.0713, null, 0.69337, null, 0.473, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28150, "SRR26209684", "SRX21920655", "SRS19005174", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 K1 2", "GSM7812984", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K1|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 K1 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K1|treatment:unDMSO", "GSM7812984", "GSM7812984: unDMSO t1 K1 2; Danio rerio; RNA Seq", "GSM7812984 r1", "GSM7812984", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A32_S50_L007_R1_001.fastq.gz", "fastq", 472785040.0, 4681040.0, "GSM7812984 r3", "0:101", "A:116503463;C:114489771;G:108989839;T:132797698;N:4269", 101, null, null, null, 116503463, 114489771, 108989839, 132797698, 4269, "SRX21920655", "SRS19005174", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94373, null, 0.07285, null, 0.69467, null, 0.47913, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28151, "SRR26209685", "SRX21920655", "SRS19005174", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 K1 2", "GSM7812984", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K1|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 K1 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K1|treatment:unDMSO", "GSM7812984", "GSM7812984: unDMSO t1 K1 2; Danio rerio; RNA Seq", "GSM7812984 r1", "GSM7812984", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A32_S71_L007_R1_001.fastq.gz", "fastq", 561056414.0, 5555014.0, "GSM7812984 r4", "0:101", "A:138240115;C:136040813;G:129592563;T:157172399;N:10524", 101, null, null, null, 138240115, 136040813, 129592563, 157172399, 10524, "SRX21920655", "SRS19005174", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94357, null, 0.07109, null, 0.69544, null, 0.47169, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28152, "SRR26209686", "SRX21920655", "SRS19005174", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 K1 2", "GSM7812984", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K1|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 K1 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K1|treatment:unDMSO", "GSM7812984", "GSM7812984: unDMSO t1 K1 2; Danio rerio; RNA Seq", "GSM7812984 r1", "GSM7812984", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A32_S71_L008_R1_001.fastq.gz", "fastq", 563109744.0, 5575344.0, "GSM7812984 r5", "0:101", "A:138778764;C:136444809;G:129964766;T:157904708;N:16697", 101, null, null, null, 138778764, 136444809, 129964766, 157904708, 16697, "SRX21920655", "SRS19005174", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94358, null, 0.07253, null, 0.69345, null, 0.47443, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28153, "SRR26209687", "SRX21920654", "SRS19005173", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 K1 1", "GSM7812983", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K1|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 K1 1", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K1|treatment:unDMSO", "GSM7812983", "GSM7812983: unDMSO t1 K1 1; Danio rerio; RNA Seq", "GSM7812983 r1", "GSM7812983", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A31_S49_L005_R1_001.fastq.gz", "fastq", 576725857.0, 5710157.0, "GSM7812983 r1", "0:101", "A:142557020;C:140092748;G:133378036;T:160693137;N:4916", 101, null, null, null, 142557020, 140092748, 133378036, 160693137, 4916, "SRX21920654", "SRS19005173", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94239, null, 0.07259, null, 0.69398, null, 0.47675, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28154, "SRR26209688", "SRX21920654", "SRS19005173", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 K1 1", "GSM7812983", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K1|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 K1 1", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K1|treatment:unDMSO", "GSM7812983", "GSM7812983: unDMSO t1 K1 1; Danio rerio; RNA Seq", "GSM7812983 r1", "GSM7812983", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A31_S49_L006_R1_001.fastq.gz", "fastq", 569166310.0, 5635310.0, "GSM7812983 r2", "0:101", "A:140702145;C:138232540;G:131558917;T:158663414;N:9294", 101, null, null, null, 140702145, 138232540, 131558917, 158663414, 9294, "SRX21920654", "SRS19005173", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94221, null, 0.07252, null, 0.69524, null, 0.4833, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28155, "SRR26209689", "SRX21920654", "SRS19005173", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 K1 1", "GSM7812983", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K1|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 K1 1", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K1|treatment:unDMSO", "GSM7812983", "GSM7812983: unDMSO t1 K1 1; Danio rerio; RNA Seq", "GSM7812983 r1", "GSM7812983", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A31_S49_L007_R1_001.fastq.gz", "fastq", 505699425.0, 5006925.0, "GSM7812983 r3", "0:101", "A:124940125;C:122891114;G:116919354;T:140944307;N:4525", 101, null, null, null, 124940125, 122891114, 116919354, 140944307, 4525, "SRX21920654", "SRS19005173", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.944, null, 0.07242, null, 0.69473, null, 0.48289, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28156, "SRR26209690", "SRX21920654", "SRS19005173", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 K1 1", "GSM7812983", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K1|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 K1 1", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K1|treatment:unDMSO", "GSM7812983", "GSM7812983: unDMSO t1 K1 1; Danio rerio; RNA Seq", "GSM7812983 r1", "GSM7812983", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A31_S27_L007_R1_001.fastq.gz", "fastq", 598624374.0, 5926974.0, "GSM7812983 r4", "0:101", "A:147863525;C:145723385;G:138724140;T:166302217;N:11107", 101, null, null, null, 147863525, 145723385, 138724140, 166302217, 11107, "SRX21920654", "SRS19005173", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94426, null, 0.07312, null, 0.69479, null, 0.48056, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28157, "SRR26209691", "SRX21920654", "SRS19005173", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "unDMSO t1 K1 1", "GSM7812983", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K1|treatment:unDMSO|geo loc name:missing|collection date:missing", "unDMSO t1 K1 1", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K1|treatment:unDMSO", "GSM7812983", "GSM7812983: unDMSO t1 K1 1; Danio rerio; RNA Seq", "GSM7812983 r1", "GSM7812983", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A31_S27_L008_R1_001.fastq.gz", "fastq", 602654072.0, 5966872.0, "GSM7812983 r5", "0:101", "A:148869054;C:146693906;G:139571739;T:167501958;N:17415", 101, null, null, null, 148869054, 146693906, 139571739, 167501958, 17415, "SRX21920654", "SRS19005173", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.9433, null, 0.0732, null, 0.69552, null, 0.47807, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28158, "SRR26209692", "SRX21920653", "SRS19005172", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "IR t2 WT 3", "GSM7812982", null, "source name:whole embryo|tissue:whole embryo|timepoint:t2|genotype:WT|treatment:IR|geo loc name:missing|collection date:missing", "IR t2 WT 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t2|genotype:WT|treatment:IR", "GSM7812982", "GSM7812982: IR t2 WT 3; Danio rerio; RNA Seq", "GSM7812982 r1", "GSM7812982", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A21_S38_L005_R1_001.fastq.gz", "fastq", 617990619.0, 6118719.0, "GSM7812982 r1", "0:101", "A:155764078;C:148642484;G:140551460;T:173027146;N:5451", 101, null, null, null, 155764078, 148642484, 140551460, 173027146, 5451, "SRX21920653", "SRS19005172", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.93982, null, 0.07316, null, 0.68801, null, 0.48964, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28159, "SRR26209693", "SRX21920653", "SRS19005172", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "IR t2 WT 3", "GSM7812982", null, "source name:whole embryo|tissue:whole embryo|timepoint:t2|genotype:WT|treatment:IR|geo loc name:missing|collection date:missing", "IR t2 WT 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t2|genotype:WT|treatment:IR", "GSM7812982", "GSM7812982: IR t2 WT 3; Danio rerio; RNA Seq", "GSM7812982 r1", "GSM7812982", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A21_S38_L006_R1_001.fastq.gz", "fastq", 612677312.0, 6066112.0, "GSM7812982 r2", "0:101", "A:154425053;C:147379484;G:139208932;T:171653577;N:10266", 101, null, null, null, 154425053, 147379484, 139208932, 171653577, 10266, "SRX21920653", "SRS19005172", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.93954, null, 0.07439, null, 0.68945, null, 0.48768, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28160, "SRR26209694", "SRX21920653", "SRS19005172", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "IR t2 WT 3", "GSM7812982", null, "source name:whole embryo|tissue:whole embryo|timepoint:t2|genotype:WT|treatment:IR|geo loc name:missing|collection date:missing", "IR t2 WT 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t2|genotype:WT|treatment:IR", "GSM7812982", "GSM7812982: IR t2 WT 3; Danio rerio; RNA Seq", "GSM7812982 r1", "GSM7812982", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A21_S38_L007_R1_001.fastq.gz", "fastq", 545311221.0, 5399121.0, "GSM7812982 r3", "0:101", "A:137422024;C:131281461;G:123803444;T:152799164;N:5128", 101, null, null, null, 137422024, 131281461, 123803444, 152799164, 5128, "SRX21920653", "SRS19005172", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94119, null, 0.07433, null, 0.6886, null, 0.48763, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28161, "SRR26209695", "SRX21920653", "SRS19005172", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "IR t2 WT 3", "GSM7812982", null, "source name:whole embryo|tissue:whole embryo|timepoint:t2|genotype:WT|treatment:IR|geo loc name:missing|collection date:missing", "IR t2 WT 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t2|genotype:WT|treatment:IR", "GSM7812982", "GSM7812982: IR t2 WT 3; Danio rerio; RNA Seq", "GSM7812982 r1", "GSM7812982", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A21_S68_L007_R1_001.fastq.gz", "fastq", 643233246.0, 6368646.0, "GSM7812982 r4", "0:101", "A:162062613;C:155064589;G:146625670;T:179468362;N:12012", 101, null, null, null, 162062613, 155064589, 146625670, 179468362, 12012, "SRX21920653", "SRS19005172", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94076, null, 0.07335, null, 0.68747, null, 0.48953, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28162, "SRR26209696", "SRX21920653", "SRS19005172", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "IR t2 WT 3", "GSM7812982", null, "source name:whole embryo|tissue:whole embryo|timepoint:t2|genotype:WT|treatment:IR|geo loc name:missing|collection date:missing", "IR t2 WT 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t2|genotype:WT|treatment:IR", "GSM7812982", "GSM7812982: IR t2 WT 3; Danio rerio; RNA Seq", "GSM7812982 r1", "GSM7812982", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A21_S68_L008_R1_001.fastq.gz", "fastq", 643010339.0, 6366439.0, "GSM7812982 r5", "0:101", "A:161939065;C:154897858;G:146526716;T:179627762;N:18938", 101, null, null, null, 161939065, 154897858, 146526716, 179627762, 18938, "SRX21920653", "SRS19005172", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94077, null, 0.07428, null, 0.68852, null, 0.4878, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28163, "SRR26209697", "SRX21920652", "SRS19005171", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "IR t2 WT 2", "GSM7812981", null, "source name:whole embryo|tissue:whole embryo|timepoint:t2|genotype:WT|treatment:IR|geo loc name:missing|collection date:missing", "IR t2 WT 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t2|genotype:WT|treatment:IR", "GSM7812981", "GSM7812981: IR t2 WT 2; Danio rerio; RNA Seq", "GSM7812981 r1", "GSM7812981", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A20_S37_L005_R1_001.fastq.gz", "fastq", 608303002.0, 6022802.0, "GSM7812981 r1", "0:101", "A:151266125;C:146608795;G:139308397;T:171114479;N:5206", 101, null, null, null, 151266125, 146608795, 139308397, 171114479, 5206, "SRX21920652", "SRS19005171", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.9409, null, 0.06934, null, 0.68702, null, 0.48691, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28164, "SRR26209698", "SRX21920652", "SRS19005171", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "IR t2 WT 2", "GSM7812981", null, "source name:whole embryo|tissue:whole embryo|timepoint:t2|genotype:WT|treatment:IR|geo loc name:missing|collection date:missing", "IR t2 WT 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t2|genotype:WT|treatment:IR", "GSM7812981", "GSM7812981: IR t2 WT 2; Danio rerio; RNA Seq", "GSM7812981 r1", "GSM7812981", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A20_S37_L006_R1_001.fastq.gz", "fastq", 602278857.0, 5963157.0, "GSM7812981 r2", "0:101", "A:149885037;C:145060278;G:137831227;T:169492101;N:10214", 101, null, null, null, 149885037, 145060278, 137831227, 169492101, 10214, "SRX21920652", "SRS19005171", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94168, null, 0.06967, null, 0.68491, null, 0.48684, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28165, "SRR26209699", "SRX21920652", "SRS19005171", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "IR t2 WT 2", "GSM7812981", null, "source name:whole embryo|tissue:whole embryo|timepoint:t2|genotype:WT|treatment:IR|geo loc name:missing|collection date:missing", "IR t2 WT 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t2|genotype:WT|treatment:IR", "GSM7812981", "GSM7812981: IR t2 WT 2; Danio rerio; RNA Seq", "GSM7812981 r1", "GSM7812981", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A20_S37_L007_R1_001.fastq.gz", "fastq", 539699863.0, 5343563.0, "GSM7812981 r3", "0:101", "A:134101752;C:130207416;G:123553593;T:151832349;N:4753", 101, null, null, null, 134101752, 130207416, 123553593, 151832349, 4753, "SRX21920652", "SRS19005171", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94262, null, 0.06995, null, 0.68605, null, 0.48097, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28166, "SRR26209700", "SRX21920652", "SRS19005171", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "IR t2 WT 2", "GSM7812981", null, "source name:whole embryo|tissue:whole embryo|timepoint:t2|genotype:WT|treatment:IR|geo loc name:missing|collection date:missing", "IR t2 WT 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t2|genotype:WT|treatment:IR", "GSM7812981", "GSM7812981: IR t2 WT 2; Danio rerio; RNA Seq", "GSM7812981 r1", "GSM7812981", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A20_S13_L007_R1_001.fastq.gz", "fastq", 629529263.0, 6232963.0, "GSM7812981 r4", "0:101", "A:156345013;C:152106432;G:144536894;T:176529480;N:11444", 101, null, null, null, 156345013, 152106432, 144536894, 176529480, 11444, "SRX21920652", "SRS19005171", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94267, null, 0.06864, null, 0.68477, null, 0.47912, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28167, "SRR26209701", "SRX21920652", "SRS19005171", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "IR t2 WT 2", "GSM7812981", null, "source name:whole embryo|tissue:whole embryo|timepoint:t2|genotype:WT|treatment:IR|geo loc name:missing|collection date:missing", "IR t2 WT 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t2|genotype:WT|treatment:IR", "GSM7812981", "GSM7812981: IR t2 WT 2; Danio rerio; RNA Seq", "GSM7812981 r1", "GSM7812981", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A20_S13_L008_R1_001.fastq.gz", "fastq", 633828732.0, 6275532.0, "GSM7812981 r5", "0:101", "A:157411401;C:153033686;G:145422340;T:177942918;N:18387", 101, null, null, null, 157411401, 153033686, 145422340, 177942918, 18387, "SRX21920652", "SRS19005171", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94386, null, 0.06993, null, 0.68479, null, 0.48216, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28168, "SRR26209702", "SRX21920651", "SRS19005170", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 WT 3", "GSM7813000", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:WT|treatment:un|geo loc name:missing|collection date:missing", "un t1 WT 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:WT|treatment:un", "GSM7813000", "GSM7813000: un t1 WT 3; Danio rerio; RNA Seq", "GSM7813000 r1", "GSM7813000", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A3_S47_L005_R1_001.fastq.gz", "fastq", 576015423.0, 5703123.0, "GSM7813000 r1", "0:101", "A:142483427;C:134492274;G:128574929;T:170459571;N:5222", 101, null, null, null, 142483427, 134492274, 128574929, 170459571, 5222, "SRX21920651", "SRS19005170", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.93576, null, 0.07681, null, 0.6939, null, 0.4794, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28169, "SRR26209703", "SRX21920651", "SRS19005170", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 WT 3", "GSM7813000", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:WT|treatment:un|geo loc name:missing|collection date:missing", "un t1 WT 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:WT|treatment:un", "GSM7813000", "GSM7813000: un t1 WT 3; Danio rerio; RNA Seq", "GSM7813000 r1", "GSM7813000", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A3_S47_L006_R1_001.fastq.gz", "fastq", 568813012.0, 5631812.0, "GSM7813000 r2", "0:101", "A:140699035;C:132793802;G:126863421;T:168447319;N:9435", 101, null, null, null, 140699035, 132793802, 126863421, 168447319, 9435, "SRX21920651", "SRS19005170", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.93455, null, 0.07506, null, 0.69229, null, 0.47926, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28170, "SRR26209704", "SRX21920651", "SRS19005170", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 WT 3", "GSM7813000", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:WT|treatment:un|geo loc name:missing|collection date:missing", "un t1 WT 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:WT|treatment:un", "GSM7813000", "GSM7813000: un t1 WT 3; Danio rerio; RNA Seq", "GSM7813000 r1", "GSM7813000", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A3_S47_L007_R1_001.fastq.gz", "fastq", 510666908.0, 5056108.0, "GSM7813000 r3", "0:101", "A:126264547;C:119308486;G:114018656;T:151070721;N:4498", 101, null, null, null, 126264547, 119308486, 114018656, 151070721, 4498, "SRX21920651", "SRS19005170", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.93621, null, 0.07582, null, 0.6928, null, 0.48424, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28171, "SRR26209705", "SRX21920651", "SRS19005170", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 WT 3", "GSM7813000", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:WT|treatment:un|geo loc name:missing|collection date:missing", "un t1 WT 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:WT|treatment:un", "GSM7813000", "GSM7813000: un t1 WT 3; Danio rerio; RNA Seq", "GSM7813000 r1", "GSM7813000", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A3_S5_L007_R1_001.fastq.gz", "fastq", 602866980.0, 5968980.0, "GSM7813000 r4", "0:101", "A:148987273;C:141267314;G:134805122;T:177796181;N:11090", 101, null, null, null, 148987273, 141267314, 134805122, 177796181, 11090, "SRX21920651", "SRS19005170", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.93771, null, 0.07611, null, 0.69305, null, 0.48012, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28172, "SRR26209706", "SRX21920651", "SRS19005170", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 WT 3", "GSM7813000", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:WT|treatment:un|geo loc name:missing|collection date:missing", "un t1 WT 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:WT|treatment:un", "GSM7813000", "GSM7813000: un t1 WT 3; Danio rerio; RNA Seq", "GSM7813000 r1", "GSM7813000", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A3_S5_L008_R1_001.fastq.gz", "fastq", 605447934.0, 5994534.0, "GSM7813000 r5", "0:101", "A:149696103;C:141763945;G:135323063;T:178646888;N:17935", 101, null, null, null, 149696103, 141763945, 135323063, 178646888, 17935, "SRX21920651", "SRS19005170", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.93786, null, 0.0763, null, 0.6911, null, 0.48344, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28173, "SRR26209709", "SRX21920650", "SRS19005168", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 WT 2", "GSM7812999", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:WT|treatment:un|geo loc name:missing|collection date:missing", "un t1 WT 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:WT|treatment:un", "GSM7812999", "GSM7812999: un t1 WT 2; Danio rerio; RNA Seq", "GSM7812999 r1", "GSM7812999", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A2_S36_L005_R1_001.fastq.gz", "fastq", 556466166.0, 5509566.0, "GSM7812999 r1", "0:101", "A:139611141;C:131729703;G:125284158;T:159836124;N:5040", 101, null, null, null, 139611141, 131729703, 125284158, 159836124, 5040, "SRX21920650", "SRS19005168", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.93631, null, 0.07619, null, 0.69016, null, 0.47322, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28174, "SRR26209710", "SRX21920650", "SRS19005168", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 WT 2", "GSM7812999", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:WT|treatment:un|geo loc name:missing|collection date:missing", "un t1 WT 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:WT|treatment:un", "GSM7812999", "GSM7812999: un t1 WT 2; Danio rerio; RNA Seq", "GSM7812999 r1", "GSM7812999", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A2_S36_L006_R1_001.fastq.gz", "fastq", 550955707.0, 5455007.0, "GSM7812999 r2", "0:101", "A:138283185;C:130378801;G:123913867;T:158370327;N:9527", 101, null, null, null, 138283185, 130378801, 123913867, 158370327, 9527, "SRX21920650", "SRS19005168", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.93674, null, 0.07558, null, 0.69018, null, 0.47446, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28175, "SRR26209711", "SRX21920650", "SRS19005168", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 WT 2", "GSM7812999", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:WT|treatment:un|geo loc name:missing|collection date:missing", "un t1 WT 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:WT|treatment:un", "GSM7812999", "GSM7812999: un t1 WT 2; Danio rerio; RNA Seq", "GSM7812999 r1", "GSM7812999", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A2_S36_L007_R1_001.fastq.gz", "fastq", 489105125.0, 4842625.0, "GSM7812999 r3", "0:101", "A:122641903;C:115831859;G:110132706;T:140494104;N:4553", 101, null, null, null, 122641903, 115831859, 110132706, 140494104, 4553, "SRX21920650", "SRS19005168", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.93871, null, 0.07529, null, 0.69067, null, 0.47657, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28176, "SRR26209712", "SRX21920650", "SRS19005168", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 WT 2", "GSM7812999", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:WT|treatment:un|geo loc name:missing|collection date:missing", "un t1 WT 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:WT|treatment:un", "GSM7812999", "GSM7812999: un t1 WT 2; Danio rerio; RNA Seq", "GSM7812999 r1", "GSM7812999", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A2_S52_L007_R1_001.fastq.gz", "fastq", 584149862.0, 5783662.0, "GSM7812999 r4", "0:101", "A:146448684;C:138570019;G:131766472;T:167353726;N:10961", 101, null, null, null, 146448684, 138570019, 131766472, 167353726, 10961, "SRX21920650", "SRS19005168", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.93862, null, 0.07597, null, 0.69037, null, 0.47425, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28177, "SRR26209713", "SRX21920650", "SRS19005168", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 WT 2", "GSM7812999", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:WT|treatment:un|geo loc name:missing|collection date:missing", "un t1 WT 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:WT|treatment:un", "GSM7812999", "GSM7812999: un t1 WT 2; Danio rerio; RNA Seq", "GSM7812999 r1", "GSM7812999", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A2_S52_L008_R1_001.fastq.gz", "fastq", 587223595.0, 5814095.0, "GSM7812999 r5", "0:101", "A:147280051;C:139251420;G:132358015;T:168316824;N:17285", 101, null, null, null, 147280051, 139251420, 132358015, 168316824, 17285, "SRX21920650", "SRS19005168", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.93908, null, 0.07566, null, 0.69051, null, 0.47457, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28178, "SRR26209714", "SRX21920649", "SRS19005169", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 WT 1", "GSM7812998", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:WT|treatment:un|geo loc name:missing|collection date:missing", "un t1 WT 1", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:WT|treatment:un", "GSM7812998", "GSM7812998: un t1 WT 1; Danio rerio; RNA Seq", "GSM7812998 r1", "GSM7812998", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A1_S25_L005_R1_001.fastq.gz", "fastq", 586786669.0, 5809769.0, "GSM7812998 r1", "0:101", "A:146663914;C:138395633;G:131925721;T:169796344;N:5057", 101, null, null, null, 146663914, 138395633, 131925721, 169796344, 5057, "SRX21920649", "SRS19005169", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.93799, null, 0.0785, null, 0.68921, null, 0.47635, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28179, "SRR26209715", "SRX21920649", "SRS19005169", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 WT 1", "GSM7812998", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:WT|treatment:un|geo loc name:missing|collection date:missing", "un t1 WT 1", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:WT|treatment:un", "GSM7812998", "GSM7812998: un t1 WT 1; Danio rerio; RNA Seq", "GSM7812998 r1", "GSM7812998", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A1_S25_L006_R1_001.fastq.gz", "fastq", 580037142.0, 5742942.0, "GSM7812998 r2", "0:101", "A:145023616;C:136736616;G:130314515;T:167952749;N:9646", 101, null, null, null, 145023616, 136736616, 130314515, 167952749, 9646, "SRX21920649", "SRS19005169", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.9375, null, 0.0778, null, 0.69126, null, 0.4693, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28180, "SRR26209716", "SRX21920649", "SRS19005169", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 WT 1", "GSM7812998", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:WT|treatment:un|geo loc name:missing|collection date:missing", "un t1 WT 1", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:WT|treatment:un", "GSM7812998", "GSM7812998: un t1 WT 1; Danio rerio; RNA Seq", "GSM7812998 r1", "GSM7812998", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A1_S25_L007_R1_001.fastq.gz", "fastq", 520166160.0, 5150160.0, "GSM7812998 r3", "0:101", "A:129930970;C:122767131;G:117052309;T:150411128;N:4622", 101, null, null, null, 129930970, 122767131, 117052309, 150411128, 4622, "SRX21920649", "SRS19005169", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.93856, null, 0.07769, null, 0.68986, null, 0.47872, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28181, "SRR26209717", "SRX21920649", "SRS19005169", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 WT 1", "GSM7812998", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:WT|treatment:un|geo loc name:missing|collection date:missing", "un t1 WT 1", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:WT|treatment:un", "GSM7812998", "GSM7812998: un t1 WT 1; Danio rerio; RNA Seq", "GSM7812998 r1", "GSM7812998", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A1_S38_L007_R1_001.fastq.gz", "fastq", 613687716.0, 6076116.0, "GSM7812998 r4", "0:101", "A:153144671;C:145096423;G:138249991;T:177185506;N:11125", 101, null, null, null, 153144671, 145096423, 138249991, 177185506, 11125, "SRX21920649", "SRS19005169", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.93852, null, 0.07714, null, 0.69114, null, 0.47286, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28182, "SRR26209718", "SRX21920649", "SRS19005169", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 WT 1", "GSM7812998", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:WT|treatment:un|geo loc name:missing|collection date:missing", "un t1 WT 1", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:WT|treatment:un", "GSM7812998", "GSM7812998: un t1 WT 1; Danio rerio; RNA Seq", "GSM7812998 r1", "GSM7812998", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A1_S38_L008_R1_001.fastq.gz", "fastq", 616318665.0, 6102165.0, "GSM7812998 r5", "0:101", "A:153949045;C:145626513;G:138751875;T:177973081;N:18151", 101, null, null, null, 153949045, 145626513, 138751875, 177973081, 18151, "SRX21920649", "SRS19005169", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.93903, null, 0.07786, null, 0.68988, null, 0.47636, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28183, "SRR26209719", "SRX21920648", "SRS19005167", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 K2 3", "GSM7812997", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K2|treatment:un|geo loc name:missing|collection date:missing", "un t1 K2 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K2|treatment:un", "GSM7812997", "GSM7812997: un t1 K2 3; Danio rerio; RNA Seq", "GSM7812997 r1", "GSM7812997", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A9_S78_L005_R1_001.fastq.gz", "fastq", 724244336.0, 7170736.0, "GSM7812997 r1", "0:101", "A:186549355;C:171075233;G:162480404;T:204132811;N:6533", 101, null, null, null, 186549355, 171075233, 162480404, 204132811, 6533, "SRX21920648", "SRS19005167", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.93859, null, 0.0781, null, 0.69398, null, 0.47368, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28184, "SRR26209720", "SRX21920648", "SRS19005167", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 K2 3", "GSM7812997", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K2|treatment:un|geo loc name:missing|collection date:missing", "un t1 K2 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K2|treatment:un", "GSM7812997", "GSM7812997: un t1 K2 3; Danio rerio; RNA Seq", "GSM7812997 r1", "GSM7812997", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A9_S78_L006_R1_001.fastq.gz", "fastq", 715170900.0, 7080900.0, "GSM7812997 r2", "0:101", "A:184237250;C:168924034;G:160306739;T:201690849;N:12028", 101, null, null, null, 184237250, 168924034, 160306739, 201690849, 12028, "SRX21920648", "SRS19005167", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.9387, null, 0.07758, null, 0.69351, null, 0.47477, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28185, "SRR26209721", "SRX21920648", "SRS19005167", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 K2 3", "GSM7812997", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K2|treatment:un|geo loc name:missing|collection date:missing", "un t1 K2 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K2|treatment:un", "GSM7812997", "GSM7812997: un t1 K2 3; Danio rerio; RNA Seq", "GSM7812997 r1", "GSM7812997", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A9_S78_L007_R1_001.fastq.gz", "fastq", 640321517.0, 6339817.0, "GSM7812997 r3", "0:101", "A:164839141;C:151424251;G:143417815;T:180634187;N:6123", 101, null, null, null, 164839141, 151424251, 143417815, 180634187, 6123, "SRX21920648", "SRS19005167", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.93922, null, 0.07776, null, 0.69704, null, 0.47799, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28186, "SRR26209722", "SRX21920648", "SRS19005167", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 K2 3", "GSM7812997", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K2|treatment:un|geo loc name:missing|collection date:missing", "un t1 K2 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K2|treatment:un", "GSM7812997", "GSM7812997: un t1 K2 3; Danio rerio; RNA Seq", "GSM7812997 r1", "GSM7812997", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A9_S40_L007_R1_001.fastq.gz", "fastq", 761823507.0, 7542807.0, "GSM7812997 r4", "0:101", "A:196286252;C:180257625;G:171369071;T:213896271;N:14288", 101, null, null, null, 196286252, 180257625, 171369071, 213896271, 14288, "SRX21920648", "SRS19005167", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.9401, null, 0.07711, null, 0.69432, null, 0.47434, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28187, "SRR26209723", "SRX21920648", "SRS19005167", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 K2 3", "GSM7812997", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K2|treatment:un|geo loc name:missing|collection date:missing", "un t1 K2 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K2|treatment:un", "GSM7812997", "GSM7812997: un t1 K2 3; Danio rerio; RNA Seq", "GSM7812997 r1", "GSM7812997", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A9_S40_L008_R1_001.fastq.gz", "fastq", 766290434.0, 7587034.0, "GSM7812997 r5", "0:101", "A:197350392;C:181234905;G:172326999;T:215355106;N:23032", 101, null, null, null, 197350392, 181234905, 172326999, 215355106, 23032, "SRX21920648", "SRS19005167", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94063, null, 0.07837, null, 0.69286, null, 0.47547, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28188, "SRR26209724", "SRX21920647", "SRS19005166", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 K2 2", "GSM7812996", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K2|treatment:un|geo loc name:missing|collection date:missing", "un t1 K2 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K2|treatment:un", "GSM7812996", "GSM7812996: un t1 K2 2; Danio rerio; RNA Seq", "GSM7812996 r1", "GSM7812996", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A8_S77_L005_R1_001.fastq.gz", "fastq", 593569122.0, 5876922.0, "GSM7812996 r1", "0:101", "A:149278073;C:141195461;G:134126340;T:168963965;N:5283", 101, null, null, null, 149278073, 141195461, 134126340, 168963965, 5283, "SRX21920647", "SRS19005166", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.93767, null, 0.07505, null, 0.69146, null, 0.4769, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28189, "SRR26209725", "SRX21920647", "SRS19005166", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 K2 2", "GSM7812996", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K2|treatment:un|geo loc name:missing|collection date:missing", "un t1 K2 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K2|treatment:un", "GSM7812996", "GSM7812996: un t1 K2 2; Danio rerio; RNA Seq", "GSM7812996 r1", "GSM7812996", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A8_S77_L006_R1_001.fastq.gz", "fastq", 589735768.0, 5838968.0, "GSM7812996 r2", "0:101", "A:148392810;C:140188863;G:133132306;T:168011761;N:10028", 101, null, null, null, 148392810, 140188863, 133132306, 168011761, 10028, "SRX21920647", "SRS19005166", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.93804, null, 0.07637, null, 0.69112, null, 0.47875, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28190, "SRR26209726", "SRX21920647", "SRS19005166", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 K2 2", "GSM7812996", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K2|treatment:un|geo loc name:missing|collection date:missing", "un t1 K2 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K2|treatment:un", "GSM7812996", "GSM7812996: un t1 K2 2; Danio rerio; RNA Seq", "GSM7812996 r1", "GSM7812996", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A8_S77_L007_R1_001.fastq.gz", "fastq", 527272217.0, 5220517.0, "GSM7812996 r3", "0:101", "A:132562535;C:125471545;G:119166731;T:150066425;N:4981", 101, null, null, null, 132562535, 125471545, 119166731, 150066425, 4981, "SRX21920647", "SRS19005166", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.93967, null, 0.07529, null, 0.69138, null, 0.47674, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28191, "SRR26209727", "SRX21920647", "SRS19005166", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 K2 2", "GSM7812996", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K2|treatment:un|geo loc name:missing|collection date:missing", "un t1 K2 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K2|treatment:un", "GSM7812996", "GSM7812996: un t1 K2 2; Danio rerio; RNA Seq", "GSM7812996 r1", "GSM7812996", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A8_S23_L007_R1_001.fastq.gz", "fastq", 625918816.0, 6197216.0, "GSM7812996 r4", "0:101", "A:157368110;C:149165182;G:141695477;T:177678522;N:11525", 101, null, null, null, 157368110, 149165182, 141695477, 177678522, 11525, "SRX21920647", "SRS19005166", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.9397, null, 0.07494, null, 0.69098, null, 0.47166, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28192, "SRR26209728", "SRX21920647", "SRS19005166", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 K2 2", "GSM7812996", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K2|treatment:un|geo loc name:missing|collection date:missing", "un t1 K2 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K2|treatment:un", "GSM7812996", "GSM7812996: un t1 K2 2; Danio rerio; RNA Seq", "GSM7812996 r1", "GSM7812996", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A8_S23_L008_R1_001.fastq.gz", "fastq", 627642987.0, 6214287.0, "GSM7812996 r5", "0:101", "A:157833602;C:149532903;G:142007778;T:178250148;N:18556", 101, null, null, null, 157833602, 149532903, 142007778, 178250148, 18556, "SRX21920647", "SRS19005166", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.93937, null, 0.07383, null, 0.69264, null, 0.46903, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28193, "SRR26209729", "SRX21920646", "SRS19005165", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 K2 1", "GSM7812995", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K2|treatment:un|geo loc name:missing|collection date:missing", "un t1 K2 1", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K2|treatment:un", "GSM7812995", "GSM7812995: un t1 K2 1; Danio rerio; RNA Seq", "GSM7812995 r1", "GSM7812995", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A7_S76_L005_R1_001.fastq.gz", "fastq", 557161753.0, 5516453.0, "GSM7812995 r1", "0:101", "A:139596521;C:131831457;G:125907167;T:159821690;N:4918", 101, null, null, null, 139596521, 131831457, 125907167, 159821690, 4918, "SRX21920646", "SRS19005165", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.93861, null, 0.07458, null, 0.69292, null, 0.47371, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28194, "SRR26209730", "SRX21920646", "SRS19005165", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 K2 1", "GSM7812995", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K2|treatment:un|geo loc name:missing|collection date:missing", "un t1 K2 1", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K2|treatment:un", "GSM7812995", "GSM7812995: un t1 K2 1; Danio rerio; RNA Seq", "GSM7812995 r1", "GSM7812995", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A7_S76_L006_R1_001.fastq.gz", "fastq", 550172856.0, 5447256.0, "GSM7812995 r2", "0:101", "A:137900064;C:130137634;G:124245600;T:157880305;N:9253", 101, null, null, null, 137900064, 130137634, 124245600, 157880305, 9253, "SRX21920646", "SRS19005165", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.93743, null, 0.07438, null, 0.6927, null, 0.46612, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28195, "SRR26209731", "SRX21920646", "SRS19005165", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 K2 1", "GSM7812995", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K2|treatment:un|geo loc name:missing|collection date:missing", "un t1 K2 1", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K2|treatment:un", "GSM7812995", "GSM7812995: un t1 K2 1; Danio rerio; RNA Seq", "GSM7812995 r1", "GSM7812995", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A7_S76_L007_R1_001.fastq.gz", "fastq", 491286321.0, 4864221.0, "GSM7812995 r3", "0:101", "A:123003877;C:116341215;G:111062034;T:140874602;N:4593", 101, null, null, null, 123003877, 116341215, 111062034, 140874602, 4593, "SRX21920646", "SRS19005165", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.93869, null, 0.07274, null, 0.69077, null, 0.47295, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28196, "SRR26209732", "SRX21920646", "SRS19005165", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 K2 1", "GSM7812995", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K2|treatment:un|geo loc name:missing|collection date:missing", "un t1 K2 1", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K2|treatment:un", "GSM7812995", "GSM7812995: un t1 K2 1; Danio rerio; RNA Seq", "GSM7812995 r1", "GSM7812995", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A7_S32_L007_R1_001.fastq.gz", "fastq", 577161975.0, 5714475.0, "GSM7812995 r4", "0:101", "A:144483271;C:136876664;G:130683956;T:165107465;N:10619", 101, null, null, null, 144483271, 136876664, 130683956, 165107465, 10619, "SRX21920646", "SRS19005165", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.93865, null, 0.07406, null, 0.69203, null, 0.46021, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28197, "SRR26209733", "SRX21920646", "SRS19005165", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 K2 1", "GSM7812995", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K2|treatment:un|geo loc name:missing|collection date:missing", "un t1 K2 1", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K2|treatment:un", "GSM7812995", "GSM7812995: un t1 K2 1; Danio rerio; RNA Seq", "GSM7812995 r1", "GSM7812995", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A7_S32_L008_R1_001.fastq.gz", "fastq", 582306208.0, 5765408.0, "GSM7812995 r5", "0:101", "A:145810013;C:138058537;G:131781643;T:166638883;N:17132", 101, null, null, null, 145810013, 138058537, 131781643, 166638883, 17132, "SRX21920646", "SRS19005165", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.93981, null, 0.07365, null, 0.6925, null, 0.47491, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28198, "SRR26209734", "SRX21920645", "SRS19005164", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 K1 3", "GSM7812994", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K1|treatment:un|geo loc name:missing|collection date:missing", "un t1 K1 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K1|treatment:un", "GSM7812994", "GSM7812994: un t1 K1 3; Danio rerio; RNA Seq", "GSM7812994 r1", "GSM7812994", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A6_S75_L005_R1_001.fastq.gz", "fastq", 585188041.0, 5793941.0, "GSM7812994 r1", "0:101", "A:146187444;C:139060409;G:132313266;T:167621845;N:5077", 101, null, null, null, 146187444, 139060409, 132313266, 167621845, 5077, "SRX21920645", "SRS19005164", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.93793, null, 0.07294, null, 0.69223, null, 0.46629, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28199, "SRR26209735", "SRX21920645", "SRS19005164", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 K1 3", "GSM7812994", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K1|treatment:un|geo loc name:missing|collection date:missing", "un t1 K1 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K1|treatment:un", "GSM7812994", "GSM7812994: un t1 K1 3; Danio rerio; RNA Seq", "GSM7812994 r1", "GSM7812994", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A6_S75_L006_R1_001.fastq.gz", "fastq", 580715559.0, 5749659.0, "GSM7812994 r2", "0:101", "A:145163669;C:137998922;G:131187804;T:166355185;N:9979", 101, null, null, null, 145163669, 137998922, 131187804, 166355185, 9979, "SRX21920645", "SRS19005164", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.93853, null, 0.0729, null, 0.69035, null, 0.47625, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28200, "SRR26209736", "SRX21920645", "SRS19005164", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 K1 3", "GSM7812994", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K1|treatment:un|geo loc name:missing|collection date:missing", "un t1 K1 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K1|treatment:un", "GSM7812994", "GSM7812994: un t1 K1 3; Danio rerio; RNA Seq", "GSM7812994 r1", "GSM7812994", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A6_S75_L007_R1_001.fastq.gz", "fastq", 517815688.0, 5126888.0, "GSM7812994 r3", "0:101", "A:129297035;C:123107269;G:117117190;T:148289396;N:4798", 101, null, null, null, 129297035, 123107269, 117117190, 148289396, 4798, "SRX21920645", "SRS19005164", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.9397, null, 0.07185, null, 0.69234, null, 0.47459, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28201, "SRR26209737", "SRX21920645", "SRS19005164", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 K1 3", "GSM7812994", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K1|treatment:un|geo loc name:missing|collection date:missing", "un t1 K1 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K1|treatment:un", "GSM7812994", "GSM7812994: un t1 K1 3; Danio rerio; RNA Seq", "GSM7812994 r1", "GSM7812994", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A6_S50_L007_R1_001.fastq.gz", "fastq", 613195038.0, 6071238.0, "GSM7812994 r4", "0:101", "A:152868207;C:146093024;G:138971001;T:175251600;N:11206", 101, null, null, null, 152868207, 146093024, 138971001, 175251600, 11206, "SRX21920645", "SRS19005164", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.93936, null, 0.07123, null, 0.69333, null, 0.47591, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28202, "SRR26209738", "SRX21920645", "SRS19005164", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 K1 3", "GSM7812994", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K1|treatment:un|geo loc name:missing|collection date:missing", "un t1 K1 3", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K1|treatment:un", "GSM7812994", "GSM7812994: un t1 K1 3; Danio rerio; RNA Seq", "GSM7812994 r1", "GSM7812994", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A6_S50_L008_R1_001.fastq.gz", "fastq", 615596717.0, 6095017.0, "GSM7812994 r5", "0:101", "A:153526888;C:146591967;G:139462033;T:175997911;N:17918", 101, null, null, null, 153526888, 146591967, 139462033, 175997911, 17918, "SRX21920645", "SRS19005164", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.93993, null, 0.07151, null, 0.6913, null, 0.47319, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28203, "SRR26209739", "SRX21920644", "SRS19005163", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 K1 2", "GSM7812993", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K1|treatment:un|geo loc name:missing|collection date:missing", "un t1 K1 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K1|treatment:un", "GSM7812993", "GSM7812993: un t1 K1 2; Danio rerio; RNA Seq", "GSM7812993 r1", "GSM7812993", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A5_S69_L005_R1_001.fastq.gz", "fastq", 577110162.0, 5713962.0, "GSM7812993 r1", "0:101", "A:143222126;C:138374184;G:131796695;T:163711998;N:5159", 101, null, null, null, 143222126, 138374184, 131796695, 163711998, 5159, "SRX21920644", "SRS19005163", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94035, null, 0.06827, null, 0.69075, null, 0.48076, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28204, "SRR26209740", "SRX21920644", "SRS19005163", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 K1 2", "GSM7812993", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K1|treatment:un|geo loc name:missing|collection date:missing", "un t1 K1 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K1|treatment:un", "GSM7812993", "GSM7812993: un t1 K1 2; Danio rerio; RNA Seq", "GSM7812993 r1", "GSM7812993", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A5_S69_L006_R1_001.fastq.gz", "fastq", 573510724.0, 5678324.0, "GSM7812993 r2", "0:101", "A:142304701;C:137466974;G:130913504;T:162815434;N:10111", 101, null, null, null, 142304701, 137466974, 130913504, 162815434, 10111, "SRX21920644", "SRS19005163", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.93982, null, 0.06886, null, 0.69359, null, 0.47999, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28205, "SRR26209741", "SRX21920644", "SRS19005163", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 K1 2", "GSM7812993", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K1|treatment:un|geo loc name:missing|collection date:missing", "un t1 K1 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K1|treatment:un", "GSM7812993", "GSM7812993: un t1 K1 2; Danio rerio; RNA Seq", "GSM7812993 r1", "GSM7812993", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A5_S69_L007_R1_001.fastq.gz", "fastq", 510919004.0, 5058604.0, "GSM7812993 r3", "0:101", "A:126655386;C:122563954;G:116745706;T:144949102;N:4856", 101, null, null, null, 126655386, 122563954, 116745706, 144949102, 4856, "SRX21920644", "SRS19005163", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94168, null, 0.06886, null, 0.69191, null, 0.47037, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28206, "SRR26209742", "SRX21920644", "SRS19005163", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 K1 2", "GSM7812993", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K1|treatment:un|geo loc name:missing|collection date:missing", "un t1 K1 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K1|treatment:un", "GSM7812993", "GSM7812993: un t1 K1 2; Danio rerio; RNA Seq", "GSM7812993 r1", "GSM7812993", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A5_S9_L007_R1_001.fastq.gz", "fastq", 605041510.0, 5990510.0, "GSM7812993 r4", "0:101", "A:149954650;C:145370877;G:138469162;T:171236044;N:10777", 101, null, null, null, 149954650, 145370877, 138469162, 171236044, 10777, "SRX21920644", "SRS19005163", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94348, null, 0.06807, null, 0.69067, null, 0.47413, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28207, "SRR26209743", "SRX21920644", "SRS19005163", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 K1 2", "GSM7812993", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K1|treatment:un|geo loc name:missing|collection date:missing", "un t1 K1 2", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K1|treatment:un", "GSM7812993", "GSM7812993: un t1 K1 2; Danio rerio; RNA Seq", "GSM7812993 r1", "GSM7812993", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A5_S9_L008_R1_001.fastq.gz", "fastq", 604369355.0, 5983855.0, "GSM7812993 r5", "0:101", "A:149836950;C:145113533;G:138254711;T:171146474;N:17687", 101, null, null, null, 149836950, 145113533, 138254711, 171146474, 17687, "SRX21920644", "SRS19005163", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94178, null, 0.06882, null, 0.69262, null, 0.47335, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", "Undetermined", "Embryo", "Whole Organism", "All anatomical structures"], [28208, "SRR26209744", "SRX21920643", "SRS19005162", "SRP463749", "PRJNA1022096", "Zebrafish reveal new roles for Fam83f in hatching and DNA damage mediated autophagic responses", "GSE244291", "Transcriptome Analysis", "The FAM83 Family with sequence similarity 83 family is highly conserved in vertebrates  yet little is known of the functions of these proteins beyond a correlation with oncogenesis. Of the family  FAM83F is of particular interest because it is the only membrane targeted FAM83 protein. FAM83F has been shown to activate the canonical Wnt signalling pathway and bind to and stabilize p53 when overexpressed  two pathways often dysregulated in disease.  Insights into gene function can often be gained by studying the roles they play during development  and here we report the generation of fam83f knock out fam83f /  zebrafish  which we have used to elucidate the role of Fam83f in vivo. We show that endogenous fam83f is most strongly expressed in the proteolytic enzyme containing hatch gland of developing zebrafish embryos  and that fam83f /  embryos hatch earlier than WT counterparts  despite developing at a comparable temporal rate. We demonstrate that fam83f /  embryos are more sensitive to ionizing radiation than WT embryos  a finding that contrasts with the previously reported role of FAM83F as a stabilizer of p53. Transcriptomic analysis shows that loss of fam83f causes downregulation of phosphatidylinositol 3 phosphate PI3P binding proteins and impairment of cellular degradation pathways  particularly autophagy  which is a crucial component of the DNA damage response. Finally  we show that Fam83f protein is itself targeted to the lysosome when expressed in cultured cells  and that this localization is dependent upon a C' terminal signal sequence.  The zebrafish lines we have generated here suggest for the first time that Fam83f plays an important role in autophagic/lysosomal processes  resulting in dysregulated hatching and increased sensitivity to genotoxic stress in vivo. Overall design: fam83fa /  zebrafish are more sensitive to ionizing radiation IR than WT counterparts. We conducted bulk RNA seq on WT vs two different fam83fa /  K1 and K2 zebrafish lines by subjecting 24 hpf embryos from each genotype to IR then extracting total RNA at 2 and 10 hours following treament t1 and t2.  Three biological replicates of a minimum of 10 embryos per replicate were sequenced by bulk RNA seq to to identify any differences in the DNA damage response between WT and fam83fa /  mutants. Treatments: AD = Actinomycin D in DMSO vehicle IR = ionizing radiation 20 Grays gamma radiation unDMSO = untreated AD control vehicle only i.e. DMSO un = untreated IR control", null, "pubmed:39437839", null, "un t1 K1 1", "GSM7812992", null, "source name:whole embryo|tissue:whole embryo|timepoint:t1|genotype:K1|treatment:un|geo loc name:missing|collection date:missing", "un t1 K1 1", "Cutadapt  1.9.1 rsem 1.3.0 star 2.5.2a Assembly: GRCz11 assembly Supplementary files format and content: *.genes.results are rsem count files", "whole embryo", "Embryos were exposed to gamma IR of 20 Gy at xxx hpf", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", "Zebrafish embryos post collection were maintained at 28.5C in E2 medium at a density \u22dc  50 embryos", "tissue:whole embryo|timepoint:t1|genotype:K1|treatment:un", "GSM7812992", "GSM7812992: un t1 K1 1; Danio rerio; RNA Seq", "GSM7812992 r1", "GSM7812992", "1", "Total RNA was extracted using RNeasy Mini Kit QIAGEN rRNA depletion Rio Zero Plus rRNA Depletion Kit Ilumina  then library prep using KAPA mRNA HyperPrep Kit for Ilumina Platforms", null, "RNA-Seq", "TRANSCRIPTOMIC", "cDNA", "SINGLE", "ILLUMINA", "Illumina HiSeq 4000", null, "SRP463749", null, "loader:fastq load.py", "JON686A4_S58_L005_R1_001.fastq.gz", "fastq", 547485852.0, 5420652.0, "GSM7812992 r1", "0:101", "A:136326023;C:130857640;G:124806460;T:155490891;N:4838", 101, null, null, null, 136326023, 130857640, 124806460, 155490891, 4838, "SRX21920643", "SRS19005162", "SRA1722794", "Devenport, Molecular Biology, Princeton University", "Devenport, Molecular Biology, Princeton University", 1, 0.94052, null, 0.07162, null, 0.69372, null, 0.46973, null, 101, null, "B", null, "usable mapping rate", "illumina", "hiseq_era", "unknown", "rrna_depletion", "unknown", "bulk", "bulk", "bulk", null, "United States", "2023-09-28", 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