Modulation of ERα transcriptional activity by the orphan nuclear receptor ERRβ and evidence for differential effects of long- and short-form splice variants

被引:27
作者
Bombail, Vincent [1 ]
Collins, Frances [1 ]
Brown, Pamela [1 ]
Saunders, Philippa T. K. [1 ]
机构
[1] Queens Med Res Inst, Human Reprod Sci Unit, MRC, Ctr Reprod Biol, Edinburgh EH16 4TJ, Midlothian, Scotland
基金
英国医学研究理事会;
关键词
Oestrogen receptor; Orphan receptor; F-domain; Splice variant; ESRRB; ESTROGEN-RELATED-RECEPTOR; F-DOMAIN; C-MYC; RESPONSE ELEMENTS; BINDING; GENE; IDENTIFICATION; ACTIVATION; EXPRESSION; COACTIVATOR;
D O I
10.1016/j.mce.2009.09.007
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Oestrogen receptor related proteins (ERRs) affect target gene expression without binding oestradiol. We investigated the functional activity of two splice variant isoforms of ERR beta (ERR beta S [short], ERR beta L [long]) expressed in human endometrium, where they are coexpressed with the oestrogen receptor alpha (ER alpha). Over-expression of ERR beta L enhanced ER alpha-dependent ligand-induced activation of an ERE-luciferase reporter construct, altered the induction of c-myc mRNA and increased proliferation of Ishikawa cells whereas ERR beta S was found to reduce these endpoints. Fluorescent recovery after photobleaching (FRAP) revealed that intra-nuclear mobility of YFP-ERR beta S was more rapid than YFP-ERR beta L Fluorescence resonance energy transfer (FRET) assays revealed a close association between ERR beta L and ER alpha following addition of ligand. We speculate that ERR beta L may alter ERa-dependent gene activation by enhancing the recruitment of co-activators. In conclusion, variant isoforms of ERRP have differential effects on ER alpha-dependent gene expression and this has implications for human endometrial cell function. (C) 2009 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:53 / 61
页数:9
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