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人钠氢交换调节因子/埃兹蛋白-根蛋白-膜突蛋白结合蛋白50(NHE-RF/EBP50)基因的雌激素受体诱导性涉及多个半雌激素反应元件。

Estrogen receptor inducibility of the human Na+/H+ exchanger regulatory factor/ezrin-radixin-moesin binding protein 50 (NHE-RF/EBP50) gene involving multiple half-estrogen response elements.

作者信息

Ediger Tracy R, Park Seong-Eun, Katzenellenbogen Benita S

机构信息

Department of Cell and Structural Biology, University of Illinois and College of Medicine, Urbana, Illinois 61801-3704, USA.

出版信息

Mol Endocrinol. 2002 Aug;16(8):1828-39. doi: 10.1210/me.2001-0290.

DOI:10.1210/me.2001-0290
PMID:12145337
Abstract

The Na+/H+ exchanger regulatory factor (NHE-RF; also known as ezrin-radixin-moesin binding protein 50) is a primary response gene under estrogen receptor (ER) control that may provide a link between estrogen action and the regulation of cytoskeletal and cell-signaling pathways. These studies were undertaken to define the human NHE-RF genomic regions and regulatory sequences mediating its robust estrogen responsiveness. Screening of a human genomic library yielded NHE-RF clones comprising the full gene, including the 5'-regulatory region and first exon, which were found to contain a large number (13) of consensus half-estrogen response elements (EREs), but to lack palindromic full EREs. Transfection-transactivation assays with wild-type and mutant ERs and reporter gene constructs linked to progressive deletions, or containing mutations, of the 5'-flanking region including a portion of exon I, and electrophoretic mobility and competitive gel shift assays were performed. These demonstrated direct ER interaction with the multiple half-ERE sites and the importance of the one proximal half-ERE and the multiple upstream half-EREs for eliciting the robust transcription activation of the NHE-RF gene by the estrogen-ER complex. Our findings highlight a paradigm for gene regulation via numerous half-ERE sites that expands the range of modes by which DNA recognition sites mediate the actions of this nuclear receptor.

摘要

钠/氢交换调节因子(NHE-RF;也称为埃兹蛋白-根蛋白-膜突蛋白结合蛋白50)是雌激素受体(ER)调控下的一个初级反应基因,它可能在雌激素作用与细胞骨架及细胞信号通路调控之间建立联系。开展这些研究是为了确定介导人NHE-RF强大雌激素反应性的基因组区域和调控序列。对人基因组文库进行筛选,获得了包含完整基因的NHE-RF克隆,包括5'调控区和第一个外显子,发现其含有大量(13个)共有半雌激素反应元件(ERE),但缺乏回文全ERE。用野生型和突变型ER以及与5'侧翼区(包括外显子I的一部分)的渐进缺失连接或含有突变的报告基因构建体进行转染-反式激活测定,并进行电泳迁移率和竞争性凝胶迁移试验。这些实验证明了ER与多个半ERE位点的直接相互作用,以及一个近端半ERE和多个上游半ERE对于雌激素-ER复合物引发NHE-RF基因强大转录激活的重要性。我们的研究结果突出了一种通过众多半ERE位点进行基因调控的模式,这种模式扩展了DNA识别位点介导该核受体作用的方式范围。

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