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Series GSE25694 Query DataSets for GSE25694
Status Public on Feb 05, 2011
Title [E-MTAB-115] ChIP-seq for FOXA2 HNF4a and NRF2 / GABP in HepG2
Organism Homo sapiens
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary In each cell type the expression of genes is regulated by the action of a large number of transcription factors, but so far we have only a rudimentary knowledge of the location of the gene regulatory elements where they bind. This can now be addressed with genome-wide ChIP experiments. In a previous ChIP-chip study of USF1 and USF2 we found evidence also of binding of GABP, FOXA2 and HNF4a within the enriched regions. Here we have applied ChIP-seq for these transcription factors and identified 3064 peaks of enrichment for GABP, 7266 for FOXA2 and 18783 for HNF4a. HNF4a and FOXA2 binding was found in at least half of the regions previously identified as bound by USF2 but not USF1, showing that they frequently bind the same regulatory elements. GABP peaks were found at transcription start sites whereas 94 % of FOXA2 and 90 % of HNF4a peaks were located at other positions. We developed a method based on the high resolution achieved by ChIP-seq to accurately define TFBS within peaks, and found the predicted sites to have an elevated conservation level compared to peak centers; however the majority of bindings were not evolutionary conserved. An unexpected interaction between HNF4a and GABP was seen at TSS, with as many as 1/3 of the HNF4a positive promoters being bound also by GABP, and co-immunoprecipitations show that these factors are in the same complex in the nucleus.

ArrayExpress Release Date: 2009-06-10

Publication Title: Molecular interactions between HNF4a, FOXA2 and GABP identified at regulatory DNA elements through ChIP-sequencing
Publication Author List: Ola Wallerman, Mehdi Motallebipour, Stefan Enroth, Kalicharan Patra, MadhuSudan Reddy Bysani, Jan Komorowski, Claes Wadelius

Person Roles: submitter
Person Last Name: Wallerman
Person First Name: Ola
Person Mid Initials:
Person Email: ola.wallerman@genpat.uu.se
Person Phone:
Person Address: IGP, Rudbecklab
Person Affiliation: Uppsala University

 
Overall design Experimental Design: high_throughput_sequencing_design
Experimental Design: binding_site_identification_design
Experimental Design: transcription profiling by high throughput sequencing
Experimental Factor Name: IMMUNOPRECIPITATE
Experimental Factor Name: LIBRARY_FRAGMENT_SIZE
Experimental Factor Type: immunoprecipitate
Experimental Factor Type: protocol
 
Citation(s) 19822575
Submission date Nov 29, 2010
Last update date Feb 21, 2019
Organization European Bioinformatics Institute
E-mail(s) miamexpress@ebi.ac.uk
Lab ArrayExpress
Street address Wellcome Trust Genome Campus
City Hinxton
State/province Cambridgeshire
ZIP/Postal code CB10 1SD
Country United Kingdom
 
Platforms (1)
GPL9052 Illumina Genome Analyzer (Homo sapiens)
Samples (11)
GSM630942 [E-MTAB-115] FOXA2_rep1long_lane_6.um.eland_rep1
GSM630943 [E-MTAB-115] FOXA2_rep1long_lane_7.um.eland
GSM630944 [E-MTAB-115] FOXA2_rep1short_lane_3.um.eland
Relations
ArrayExpress E-MTAB-115
BioProject PRJNA135845

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
GSE25694_RAW.tar 751.6 Mb (http)(custom) TAR (of TXT)
Raw data not provided for this record
Processed data provided as supplementary file

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