| Literature DB >> 24569880 |
Ziad Al Tanoury1, Samia Gaouar, Aleksandr Piskunov, Tao Ye, Sylvia Urban, Bernard Jost, Céline Keime, Irwin Davidson, Andrée Dierich, Cécile Rochette-Egly.
Abstract
Retinoic acid (RA) plays key roles in cell differentiation and growth arrest by activating nuclear RA receptors (RARs) (α, β and γ), which are ligand-dependent transcription factors. RARs are also phosphorylated in response to RA. Here, we investigated the in vivo relevance of the phosphorylation of RARs during RA-induced neuronal differentiation of mouse embryonic stem cells (mESCs). Using ESCs where the genes encoding each RAR subtype had been inactivated, and stable rescue lines expressing RARs mutated in phospho-acceptor sites, we show that RA-induced neuronal differentiation involves RARγ2 and requires RARγ2 phosphorylation. By gene expression profiling, we found that the phosphorylated form of RARγ2 regulates a small subset of genes through binding an unusual RA response element consisting of two direct repeats with a seven-base-pair spacer. These new findings suggest an important role for RARγ phosphorylation during cell differentiation and pave the way for further investigations during embryonic development.Entities:
Keywords: Differentiation; Nuclear receptor; Phosphorylation; RA; RAR; Retinoic acid; Transcription
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Year: 2014 PMID: 24569880 DOI: 10.1242/jcs.145979
Source DB: PubMed Journal: J Cell Sci ISSN: 0021-9533 Impact factor: 5.285