run_metadata: 71957
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| 71957 | SRR22143711 | SRX18123007 | SRS15624881 | SRP405931 | PRJNA896973 | Vitamin D Receptor regulation of hepatic energy metabolism in zebrafish | GSE217120 | Transcriptome Analysis | Vitamin D deficiency and mutations in Vitamin D Receptor VDR are associated with liver disease and obesity but the functions of vitamin D signaling in metabolism are poorly understood. Though vitamin D signaling is best known for its functions in mineral homeostasis and skeleton calcification in terrestrial vertebrates this is unlikely to be the evolutionary function of vitamin D signaling. We utilize tissue specific genetic modulation of Vdr signaling to investigate the function of the vitamin D endocrine system in zebrafish. We find that hepatocyte Vdr regulates organismal response to nutritional cues and coordinates hepatic and organismal energy metabolism by balancing energy storage and tissue growth. Overall design: Comparative gene expression profiling analysis of RNA seq data following hepatocyte specific Vdr modulation in larval and adult zebrafish. fabp10a:dn vdra and fabp10a:ca vdra transgenes were used to achieve hepatocyte Vdr impairment or hyperactivation respectively. Larval experiments were performed on sorted hepatocytes at 96 hpf and reflect approximately 35 pooled fish per sample. Adult experiments were performed on dissected male liver collected at 4.5 mpf mpf and are composed of 3 livers per sample. wild type controls are included for each experiment. For larval fabp10a:dn vdra N = 4 wt 4 dn vdra. For fabp10a:ca vdra N = 4 wt 3 ca vdra. For adult fabp10a:dn vdra N = 4 wt 4 dn vdra. | pubmed:38944835 | hepatocytes 96hpf cavdra expt2 rep3 | GSM6705365 | tissue:hepatocytes sorted|cell type:hepatocytes sorted|genotype:fabp10a:ca vdra|time:96 hpf | hepatocytes 96hpf cavdra expt2 rep3 | FASTQ files were mapped to GRCz11 using STAR v2.5.3 and read counting was performed using HTSeq v0.11.1. Read count normalization was performed using the R package DEseq2. Assembly: GRCz11 Supplementary files format and content: .csv files containing ensembl ids gene names and raw read counts or normalized read counts for each experiment | hepatocytes sorted | Hepatocytes were sorted into 75 uL Buffer RLT containing b mercaptoethanol. Total RNA was extracted using the Qiagen RNA Micro Kit with on column DNase treatment. cDNA synthesis and amplification were performed according to the Smart seq2 protocol https://doi.org/10.1038/nprot.2014.006. Library prep was performed with the Nextera XT DNA Library Preparation Kit Illumina. | Larval zebrafish were reared at 28.5 C in E3 salt solution. Adult fish were reared in density matched tanks and fed artemia twice daily. | cell type:hepatocytes sorted|genotype:fabp10a:ca vdra|time:96 hpf | GSM6705365 | GSM6705365: hepatocytes 96hpf cavdra expt2 rep3; Danio rerio; RNA Seq | GSM6705365 r1 | GSM6705365 | 1 | Hepatocytes were sorted into 75 uL Buffer RLT containing b mercaptoethanol. Total RNA was extracted using the Qiagen RNA Micro Kit with on column DNase treatment. cDNA synthesis and amplification were performed according to the Smart seq2 protocol https://doi.org/10.1038/nprot.2014.006. Library prep was performed with the Nextera XT DNA Library Preparation Kit Illumina. | RNA-Seq | TRANSCRIPTOMIC | cDNA | SINGLE | ILLUMINA | NextSeq 500 | SRP405931 | cavdra_expt2_rep3_R1.fastq.gz | fastq | 6706002750.0 | 44706685.0 | GSM6705365 r1 | 0:150 1:0 | A:1750156238;C:1597023915;G:1614921548;T:1743765130;N:135919 | 150 | 0 | 1750156238 | 1597023915 | 1614921548 | 1743765130 | 135919 | SRX18123007 | SRS15624881 | Goessling Lab, Brigham and Women's Hospital | 1 | 0.88313 | 0.04409 | 0.87661 | 0.55505 | 150 | B | usable mapping rate | illumina | nextseq | unknown | cdna_unspecified | nextera | sc | single_cell_plate | smartseq | United States | 2022-11-02 | Multi-stage | Multi-stage | Liver | Liver and Biliary System |