Journal
EMBO REPORTS
Volume 9, Issue 6, Pages 563-568Publisher
WILEY
DOI: 10.1038/embor.2008.55
Keywords
oestrogen receptor; cell cycle; chromatin-remodelling complex
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The female sex steroid hormone oestrogen stimulates both cell proliferation and cell differentiation in target tissues. These biological actions are mediated primarily through nuclear oestrogen receptors (ERs). The ligand-dependent transactivation of ERs requires several nuclear co-regulator complexes; however, the cell-cycle-dependent associations of these complexes are poorly understood. By using a synchronization system, we found that the transactivation function of ER alpha at G2/M was lowered. Biochemical approaches showed that ER alpha associated with two discrete classes of ATP-dependent chromatin-remodelling complex in a cell-cycle-dependent manner. The components of the NuRD-type complex were identified as G2/M-phase-specific ER alpha co-repressors. Thus, our results indicate that the transactivation function of ER alpha is cell-cycle dependent and is coupled with a cell-cycle-dependent association of chromatin-remodelling complexes.
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