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SRX3343441: GSM2836302: Supt16h Mutant; Danio rerio; RNA-Seq
1 ILLUMINA (Illumina HiSeq 2500) run: 43M spots, 4.3G bases, 2.5Gb downloads

Submitted by: NCBI (GEO)
Study: RNA-sequencing based linkage analysis identifies supt16h as a target gene from a forward genetic screen
show Abstracthide Abstract
Chromatin organization and accessibility are fundamental to how genes are transcriptionally controlled. We identify the first vertebrate mutant for supt16h, a component of the FACT (FAcilitates Chromatin Transcription) complex along with Ssrp1 known to reorganize nucleosomes and assist in transcriptional elongation. We demonstrate its importance in hematopoietic stem cell (HSC) specification by regulating the elongation of Notch genes. Unexpectedly, Assay for Transposase Accessible Chromatin (ATAC) sequencing revealed that loss of supt16h does not affect histone accessibility on a Notch-specific or global level. Although the majority of genes are unaffected, loss of supt16h alters chromatin accessibility significantly at the p53 locus, leading to its overexpression in mutants. Upon downregulation of p53, both loss of Notch and loss of HSC phenotypes are rescued. Notably, ssrp1 mutants possessed normal elongation of Notch genes, levels of P53, and specification of HSCs. Our results highlight the discrete effects of Supt16h and Ssrp1 during HSC specification. Additionally, we demonstrate the relationship between supt16h and p53 during transcriptional elongation to specify HSC fate via modulation of Notch signaling. Overall design: RNA-sequencing was performed on 32hpf wildtype (WT) and supt16h-/- whole embryos to perform single nucleotide polymorphism (SNP) based linkage mapping.
Sample: Supt16h Mutant
SAMN07949292 • SRS2644596 • All experiments • All runs
Organism: Danio rerio
Library:
Instrument: Illumina HiSeq 2500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: Whole embryo was collected and RNA was extracted using TriZol reagent. llumina TruSeq Stranded mRNA Library Prep Kit (Cat# RS-122-2101) was used with 1 ug of total RNA for the construction of sequencing libraries. Libraries were prepared according to Illumina's instructions accompanying the mRNA Sample Kit (Part# 15031047). Briefly, mRNA was purified using poly-T oligo magnetic beads and fragmented. Samples were subjected to first strand cDNA synthesis using SuperScript II, which was then followed by a second strand cDNA synthesis using DNA Pol I and Rnase H. The 3' ends were then adenylated and adapters are attached. The products were finally purified and PCR amplified to create the final cDNA library. Paired end 50 libraries were sequenced on the Illumina HiSeq2500.
Experiment attributes:
GEO Accession: GSM2836302
Links:
Runs: 1 run, 43M spots, 4.3G bases, 2.5Gb
Run# of Spots# of BasesSizePublished
SRR623506643,046,1954.3G2.5Gb2020-01-02

ID:
4673472

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