run_metadata: 30667
This data as json
| rowid | run.accession | experiment.accession | sample.accession | study.accession | bioproject | study.title | study.alias | study.type | study.abstract | study.attributes | study.PMIDs | sample.description | sample.title | sample.alias | sample.centername | sample.attributes | GEOsample.title | GEOsample.dataprocessing | GEOsample.source | GEOsample.treatmentprotocol | GEOsample.extractprotocol | GEOsample.growthprotocol | GEOsample.characteristics | GEOsample.accession | experiment.title | experiment.alias | experiment.library_name | experiment.design_description | experiment.library_construction_protocol | experiment.attributes | experiment.library_strategy | experiment.library_source | experiment.library_selection | experiment.library_layout | experiment.platform | experiment.instrument_model | experiment.spot_descriptor | experiment.study_ref | run.title | run.attributes | run.filename | run.semantic_name | run.total_bases | run.total_spots | run.alias | run.read_lengths | run.base_counts | run.r1_length | run.r2_length | run.r3_length | run.r4_length | run.Acount | run.Ccount | run.Gcount | run.Tcount | run.Ncount | run.experiment | run.pool_member | submission.accession | submission.srasource | submission.bioprojectsource | seqdetective.n_mates | seqdetective.mapping_rate.mate1 | seqdetective.mapping_rate.mate2 | seqdetective.nofeature_rate.mate1 | seqdetective.nofeature_rate.mate2 | seqdetective.sparsity.mate1 | seqdetective.sparsity.mate2 | seqdetective.pos_strand_rate.mate1 | seqdetective.pos_strand_rate.mate2 | seqdetective.readlen.mate1 | seqdetective.readlen.mate2 | seqdetective.judgement.mate1 | seqdetective.judgement.mate2 | seqdetective.judgement.reason | platform_family | instrument_generation | read_bias | selection_class | prep_kit | sc_or_bulk | tech_class | technology | tech_variant | submission.bioprojectsource.country | earliest_date | devstage_curation | devstage_curation_coarse | tissue_curation | tissue_curation_coarse |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 30667 | SRR28146893 | SRX23777733 | SRS20602698 | SRP492278 | PRJNA1081795 | Spring viraemia of carp virus infection induces hypoxia response in zebrafish by stabilizing hif1a | GSE260453 | Transcriptome Analysis | The hypoxia signaling pathway controls hypoxia adaptation and tolerance of organisms which is regulated by multiple mechanisms. Viral infection elicits various pathophysiological responses in the host. However whether viral infection can affect the hypoxia response is still largely unknown. In this study we found that Spring viraemia of carp virus SVCV infection in zebrafish caused symptoms similar to those in zebrafish under hypoxic conditions. Further assays indicated that SVCV infection activated the hypoxia signaling pathway in zebrafish. In addition SVCV infection caused increased glycolysis and ROS levels in cells. Mechanistically SVCV G protein interacted with hif1a a/b and attenuated their K48 linked polyubiquitination leading to their stabilization and subsequent enhancement of target gene expression. Moreover treatment with the HIF1a specific inhibitor PX478 enhanced the antiviral ability against SVCV infection in zebrafish and zebrafish cells. This study reveals a relationship between SVCV infection and the hypoxia signaling pathway in fish and provides a strategy for reducing the damage of viral disease in the aquaculture industry. Overall design: Zebrafish larvae were placed in disposable cell culture dishes 60 mm in diameter containing 4 mL of egg water and 2 mL of SVCV 5.0×107 TCID50/mL was added into each dish. Whole RNA of zebrafish larvae 3 dpf infected with or without xxx were purified using RNeasy Mini Kit QIAGEN NO. 74104. Three biological replicates were used for each sample. The transcriptome library for sequencing was generated using NEBNext Ultra RNA Library Prep Kit for Illumina NEB USA #E7530L following manufacturer's protocol In order to ensure the quality of information analysis the software fastp was used to remove the splice sequences filter the low quality N bases indicating that the base information could not be determined and obtain high quality clean data. clean data and the number of bases and sequences of the clean data were counted. At the same time GC Q20 Q30 content of the clean data were calculated GenePlus Beijing China. Heatmaps were generated using Multi Experiment Viewer MeV software. Gene Ontology GO enrichment analyses for the differentially expressed genes DEGs were performed using the cluster Profiler version 3.8. | pubmed:39601573 | zebrafish larvae svcv1 | GSM8117448 | source name:larvae|tissue:larvae|genotype:WT|treatment:svcv infection|geo loc name:missing|collection date:missing | zebrafish larvae svcv1 | Briefly mRNA was purified from total RNA using poly T oligo attached magnetic beads. Fastp version 0.19.7 was used to perform basic statistics on the quality of the raw reads. The clean reads were then mapped to the mouse genome using HISAT. Assembly: GRCz11 Supplementary files format and content: FPKM values for each Sample | larvae | Whole RNA of zebrafish larvae 3 dpf infected with or without xxx were purified using RNeasy Mini Kit QIAGEN NO. 74104. Sequencing libraries were generated using the NEB Next Ultra RNA Library Prep Kit for Illumina NEB USA #E7530L accordingly to the manufacturer’s protocol and index codes were added to assign sequences to each sample. | tissue:larvae|genotype:WT|treatment:svcv infection | GSM8117448 | GSM8117448: zebrafish larvae svcv1; Danio rerio; RNA Seq | GSM8117448 r1 | GSM8117448 | 1 | Whole RNA of zebrafish larvae 3 dpf infected with or without xxx were purified using RNeasy Mini Kit QIAGEN NO. 74104. Sequencing libraries were generated using the NEB Next Ultra RNA Library Prep Kit for Illumina NEB USA #E7530L accordingly to the manufacturer's protocol and index codes were added to assign sequences to each sample. | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP492278 | svcv-1_1.fq.gz svcv-1_2.fq.gz | fastq fastq | 10699844400.0 | 35666148.0 | GSM8117448 r1 | 0:150 1:150 | A:2874259238;C:2464699540;G:2474659412;T:2883944709;N:2281501 | 150 | 150 | 2874259238 | 2464699540 | 2474659412 | 2883944709 | 2281501 | SRX23777733 | SRS20602698 | SRA1812384 | ???????????? | 中国科学院水生生物研究所 | 2 | 0.94238 | 0.941 | 0.11297 | 0.11345 | 0.65218 | 0.65518 | 0.47212 | 0.47861 | 150 | 150 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | random_priming | nebnext | bulk | unknown | unknown | China | 2024-02-28 | Larval | Larval | Undetermined | Undetermined |