Reference : Cell-specific interaction of retinoic acid receptors with target genes in mouse embry...
Scientific journals : Article
Life sciences : Biochemistry, biophysics & molecular biology
http://hdl.handle.net/2268/102926
Cell-specific interaction of retinoic acid receptors with target genes in mouse embryonic fibroblasts and embryonic stem cells.
English
Delacroix, Laurence mailto [Université de Liège - ULg > Département des sciences cliniques > GIGA-R:Immunopath. - Maladies infect. et médec. inter. gén.]
Moutier, Emmanuel [> > > >]
Altobelli, Gioia [> > > >]
Legras, Stephanie [> > > >]
Poch, Olivier [> > > >]
Choukrallah, Mohamed-Amin [> > > >]
Bertin, Isabelle [> > > >]
Jost, Bernard [> > > >]
Davidson, Irwin [> > > >]
2010
Molecular & Cellular Biology
American Society for Microbiology (ASM)
30
1
231-44
Yes (verified by ORBi)
International
0270-7306
1098-5549
Washington
DC
[en] Amino Acid Motifs ; Animals ; Binding Sites ; Cells, Cultured ; Chromatin Immunoprecipitation ; Embryonic Stem Cells/metabolism ; Fibroblasts/metabolism ; Gene Expression Profiling ; Gene Expression Regulation ; Mice ; Oligonucleotide Array Sequence Analysis ; Receptors, Retinoic Acid/metabolism ; Transcription Factor TFIID/genetics ; Transcription Factors/metabolism
[en] All-trans retinoic acid (RA) induces transforming growth factor beta (TGF-beta)-dependent autocrine growth of mouse embryonic fibroblasts (MEFs). We have used chromatin immunoprecipitation to map 354 RA receptor (RAR) binding loci in MEFs, most of which were similarly occupied by the RAR alpha and RAR gamma receptors. Only a subset of the genes associated with these loci are regulated by RA, among which are several critical components of the TGF-beta pathway. We also show RAR binding to a novel series of target genes involved in cell cycle regulation, transformation, and metastasis, suggesting new pathways by which RA may regulate proliferation and cancer. Few of the RAR binding loci contained consensus direct-repeat (DR)-type elements. The majority comprised either degenerate DRs or no identifiable DRs but anomalously spaced half sites. Furthermore, we identify 462 RAR target loci in embryonic stem (ES) cells and show that their occupancy is cell type specific. Our results also show that differences in the chromatin landscape regulate the accessibility of a subset of more than 700 identified loci to RARs, thus modulating the repertoire of target genes that can be regulated and the biological effects of RA.
Giga-Neurosciences ; IGBMC
ANR
Researchers
http://hdl.handle.net/2268/102926
10.1128/MCB.00756-09

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