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Series GSE81628 Query DataSets for GSE81628
Status Public on Sep 06, 2016
Title Integrative genomics outlines a biphasic glucose response and a ChREBP-RORγ axis regulating proliferation in β-cells
Organism Rattus norvegicus
Experiment type Expression profiling by high throughput sequencing
Genome binding/occupancy profiling by high throughput sequencing
Summary Glucose is an important regulator of pancreatic β-cell function. In addition to the acute stimulation of insulin secretion, glucose stimulates long-term adaptive changes in gene expression that can either promote or antagonize the proliferative potential and function of β-cells. The glucose-sensing transcription factor carbohydrate response element binding protein (ChREBP) has been shown to promote both β-cell proliferation and dysfunction; however, the molecular mechanisms underlying these pleiotropic effects of ChREBP and glucose are not well understood. Here, we have generated time-resolved profiles of enhancer and transcriptional activity in response to glucose in the INS-1E pancreatic β-cell line. Our data outline a biphasic response with a first wave during which metabolic genes are activated, and a second wave where cell cycle genes are induced and β-cell identity genes are repressed. We show that ChREBP directly activates first wave genes, whereas repression and activation of second wave genes by ChREBP is indirect. By integrating motif enrichment within late-regulated enhancers with expression profiles of the associated transcription factors, we identify multiple putative regulators of the second wave, including RAR-related orphan receptor (ROR) γ, which we demonstrate is a novel direct ChREBP target gene. Importantly, we show that RORγ activity is necessary for full glucose-induced proliferation of both INS-1E and primary rat β-cells.
 
Overall design Genome-wide assesment of the transcriptional response to glucose in INS-1E β-cells using RNA- ChIP- and DNase-seq
 
Contributor(s) Schmidt SF, Mandrup S
Citation(s) 27545881
Submission date May 19, 2016
Last update date May 15, 2019
Contact name Susanne Mandrup
E-mail(s) s.mandrup@bmb.sdu.dk
Phone +45 6550 2340
Organization name University of Southern Denmark
Department Biochemistry and Molecular Biology
Street address Campusvej 55
City Odense M
ZIP/Postal code 5230
Country Denmark
 
Platforms (1)
GPL18404 Illumina HiSeq 1500 (Rattus norvegicus)
Samples (54)
GSM2159947 RNA 0h glucose A
GSM2159948 RNA 0h glucose B
GSM2159949 RNA 1h glucose A
Relations
BioProject PRJNA322158
SRA SRP075411

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
GSE81628_CAChREBP_exon.txt.gz 556.6 Kb (ftp)(http) TXT
GSE81628_ChREBP_peakfile.txt.gz 2.1 Mb (ftp)(http) TXT
GSE81628_DNase_peakfile.txt.gz 2.0 Mb (ftp)(http) TXT
GSE81628_Glucose_exon.txt.gz 1.2 Mb (ftp)(http) TXT
GSE81628_Glucose_intron.txt.gz 1.1 Mb (ftp)(http) TXT
GSE81628_Knockdowns_exon.txt.gz 2.4 Mb (ftp)(http) TXT
GSE81628_MED1_peakfile.txt.gz 1.5 Mb (ftp)(http) TXT
GSE81628_RAW.tar 666.7 Mb (http)(custom) TAR (of BEDGRAPH)
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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