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Series GSE55740 Query DataSets for GSE55740
Status Public on Dec 11, 2022
Title Analysis of the impact of FOXA1 expression on MDA::ER E2-sensitive transcriptomes and ER cistromes [ChIP-Seq data]
Organism Homo sapiens
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary The primordial actions of the estrogen receptor alpha (ER) in controlling breast cancer cells proliferation rate are particularly documented. However, reintroducing ER into ER-negative cells does not reprogram their transcriptome towards an estrogen-sensitive growth phenotype. Member of the Forkhead (FKH) family of transcription factors, FOXA1 has been characterized to be essential for the appropriate binding of ER onto chromatin in MCF-7 cells. FOXA1 pioneering actions involve modulations of histone post-translational modifications (HPTMs) and local depletion in methylated CpGs. Using MDA-MB231 cells which are ER and FOXA1 negative, we aimed at determining whether the introduction of ER and FOXA1 would be sufficient to restore an estrogen-sensitive growth and to coincidently reprogram chromatin. We used ChIP-seq experiments to map ER and FOXA1 binding sites (BSs) and to profile H3K4me2 and H3K27ac marks, and surprisingly observed that FOXA1 had rather a global negative impact on ER actions, associated with an inhibition of growth and a reorientation of the transcriptome of the cells towards cell death. We demonstrate that the re-introduction of FOXA1 in these cells actually competes for the binding and pioneering actions of FOXA2, another FKH protein, on a number of ER BSs. As demonstrated for its alter ego FOXA1 in MCF-7 cells, abrogating FOXA2 expression drastically diminished ER binding onto its cognate sites, associated with a local loss of HPTMs for active chromatin.
 
Overall design Whole-genome analysis of estrogen receptor (ER) and its FOXA1 and/or FOXA2 pioneering factors binding events associated with the cartography of two histone marks (H3K4me2 and H3K27ac) in four ER/FOXA1 positive or negative breast cancer cells.
 
Contributor(s) Quintin J, Le Péron C, Mahé E, Seérandour AA, Palierne G, Bizot M, Percevault F, Avner S, Salbert G, Métivier R
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Submission date Mar 10, 2014
Last update date Dec 12, 2022
Contact name Raphaël Métivier
E-mail(s) raphael.metivier@univ-rennes1.fr
Organization name CNRS UMR 6290
Lab SP@RTE
Street address Campus de Beaulieu
City Rennes
ZIP/Postal code 35042 Cedex
Country France
 
Platforms (2)
GPL9115 Illumina Genome Analyzer II (Homo sapiens)
GPL11154 Illumina HiSeq 2000 (Homo sapiens)
Samples (19)
GSM1342613 MDA::ER input
GSM1342614 MCF-7 input
GSM1342615 MDA::ER::pCDNA ER ChIP
This SubSeries is part of SuperSeries:
GSE55741 Analysis of the impact of FOXA1 expression on MDA::ER E2-sensitive transcriptomes and ER cistromes
Relations
BioProject PRJNA241009
SRA SRP039963

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
GSE55740_RAW.tar 5.6 Gb (http)(custom) TAR (of WIG)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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