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Series GSE197224 Query DataSets for GSE197224
Status Public on Feb 23, 2022
Title Integrating RNA-seq and assay for transposase-accessible chromatin by sequencing (ATAC-seq) predicts functionally-relevant chromatin regions
Organism Drosophila melanogaster
Experiment type Expression profiling by high throughput sequencing
Genome binding/occupancy profiling by high throughput sequencing
Summary Gene regulation is critical for proper cellular function. Next-generation sequencing technology has revealed the presence of regulatory networks that regulate gene expression and essential cellular functions. Studies investigating the epigenome have begun to uncover the complex mechanisms regulating transcription. Assay for transposase-accessible chromatin by sequencing (ATAC-seq) is quickly becoming the assay of choice for epigenomic investigations. Integrating epigenomic and transcriptomic data has the potential to reveal the chromatin-mediated mechanisms regulating transcription. However, integrating these two data types remains challenging. We used the insulin signaling pathway as a model to investigate chromatin regions and gene expression changes using ATAC- and RNA-seq in insulin-treated Drosophila S2 cells. We show that insulin causes widespread changes in chromatin accessibility and gene expression. Then, we attempted to integrate ATAC- and RNA-seq data to predict functionally-relevant chromatin regions that control the transcriptional response to insulin. We show that using differential chromatin accessibility can predict functionally-relevant genome regions, but that stratifying differentially-accessible chromatin regions by annotated feature type provides a better prediction of whether a chromatin region regulates gene expression. In particular, our data demonstrate a strong correlation between chromatin regions annotated to distal promoters (1-2 kb from the transcription start site). To test this prediction, we cloned candidate distal promoter regions upstream of luciferase and validated the functional relevance of these chromatin regions. Our data show that distal promoter regions selected by correlations with RNA-seq are more likely to control gene expression. Thus, correlating ATAC- and RNA-seq data can home in on functionally-relevant chromatin regions
 
Overall design ATAC-seq and mRNA profiles of insulin-treated Drosophila S2 cells
 
Contributor(s) Merrill CB, Montgomery AB, Pabon MA, Rodan AR, Rothenfluh A
Citation(s) 35614386
BioProject PRJNA730574
Submission date Feb 22, 2022
Last update date Jun 14, 2022
Contact name Adrian Rothenfluh
E-mail(s) adrian.rothenfluh@hsc.utah.edu
Organization name University of Utah
Department Psychiatry
Street address 15 N 2030 E
City Salt Lake City
State/province Utah
ZIP/Postal code 84132
Country USA
 
Platforms (1)
GPL17275 Illumina HiSeq 2500 (Drosophila melanogaster)
Samples (12)
GSM5911302 S2 cells - Vehicle-treated, ATAC-seq, rep1
GSM5911303 S2 cells - Vehicle-treated, ATAC-seq, rep2
GSM5911304 S2 cells - Vehicle-treated, ATAC-seq, rep3

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE197224_14989R_RNA_metrics.html.gz 396.1 Kb (ftp)(http) HTML
GSE197224_ATAC_GO_Pathways.csv.gz 7.1 Kb (ftp)(http) CSV
GSE197224_ATAC_Insulin.narrowPeak.gz 140.3 Kb (ftp)(http) NARROWPEAK
GSE197224_ATAC_Insulin_vs_Vehicle.DESeq.txt.gz 398.6 Kb (ftp)(http) TXT
GSE197224_ATAC_Peak_Annotation.xlsx 1.5 Mb (ftp)(http) XLSX
GSE197224_ATAC_Vehicle.narrowPeak.gz 138.8 Kb (ftp)(http) NARROWPEAK
GSE197224_RAW.tar 395.0 Mb (http)(custom) TAR (of BW)
GSE197224_RNA_Insulin_vs_Vehicle.DESeq.xlsx 4.5 Mb (ftp)(http) XLSX
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file
Processed data are available on Series record

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