U.S. flag

An official website of the United States government

Format

Send to:

Choose Destination

SRX24786138: GSM8302932: Test StwlEY_Replicate 3; Drosophila melanogaster; RNA-Seq
1 ILLUMINA (Illumina NovaSeq 6000) run: 28.4M spots, 2.9G bases, 863.3Mb downloads

External Id: GSM8302932_r1
Submitted by: Biology, ETH Zurich
Study: Effect of overexpession of Stonewall (Stwl) on gene expression in germline stem cell (GSC)-like cells compared to the control
show Abstracthide Abstract
The association of genomic loci to the nuclear periphery is proposed to facilitate cell type-specific gene repression and influence cell fate decisions. However, the interplay between gene position and expression remains incompletely understood, in part because the proteins that position genomic loci at the nuclear periphery remain unidentified. Here, we used an Oligopaint-based HiDRO screen targeting ~1000 genes to discover novel regulators of nuclear architecture in Drosophila cells.We identified the heterochromatin-associated protein Stonewall (Stwl) as a factor promoting perinuclear chromatin positioning. In female germline stem cells (GSCs), Stwl binds and positions chromatin loci, including GSC differentiation genes, at the nuclear periphery. Strikingly, Stwl-dependent perinuclear positioning is associated with transcriptional repression, highlighting a likely mechanism for Stwl's known role in GSC maintenance and ovary homeostasis. Thus, our study identifies perinuclear anchors in Drosophila and demonstrates the importance of gene repression at the nuclear periphery for cell fate. Overall design: To investigate the role of Stonewall on gene expression in GSCs, we enriched for GSC-like cells using genetic tools. We overexpressed Stwl in GSC-like cells and performed differential gene expression analysis using four replicates for each condition The two conditions include Control (Control_Stwl_Replicate (1-4)) or Stonewall overexpression (Test_StwlEY_Replicate (1-4))
Sample: Test StwlEY_Replicate 3
SAMN41658361 • SRS21503629 • All experiments • All runs
Library:
Name: GSM8302932
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: RNA extraction was performed using the RNA-easy kit (Qiagen). Samples were additionally treated with DNAse after extraction and RNA purification step was performed. RNA libraries were prepared by the Functional Genomic Center Zurich (FCGZ) using Tru-Seq mRNA library kit )as per manufacturer's protocol
Runs: 1 run, 28.4M spots, 2.9G bases, 863.3Mb
Run# of Spots# of BasesSizePublished
SRR2926850828,418,2252.9G863.3Mb2024-08-01

ID:
33111476

Supplemental Content

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...