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孤儿核受体雌激素受体相关受体γ对转录的脱氧核糖核酸反应元件依赖性调控

Deoxyribonucleic acid response element-dependent regulation of transcription by orphan nuclear receptor estrogen receptor-related receptor gamma.

作者信息

Sanyal Sabyasachi, Matthews Jason, Bouton Didier, Kim Han-Jong, Choi Hueng-Sik, Treuter Eckardt, Gustafsson Jan-Ake

机构信息

Department of Biosciences at Novum, Karolinska Institutet, S-14157 Huddinge, Sweden.

出版信息

Mol Endocrinol. 2004 Feb;18(2):312-25. doi: 10.1210/me.2003-0165. Epub 2003 Nov 26.

Abstract

The estrogen receptor-related receptor gamma (ERR gamma/ERR3/NR3B3) is the newest member of the ERR subfamily that also includes ERR alpha and ERR beta. All three isoforms share a high degree of amino acid identity especially in the DNA binding domain. ERR gamma is a constitutively active transcriptional activator that regulates reporter elements driven by steroidogenic factor 1 response element (SF-1RE) and estrogen response element. However, it has the highest potency on a derivative of SF-1RE present in the small heterodimer partner gene promoter called sft4 and unlike ERR alpha and -beta, it fails to activate a palindromic thyroid hormone response element. To investigate the mechanism behind this response element-specific differential transcriptional activity of ERR gamma, the interactions of ERR gamma and the aforementioned response elements was monitored. EMSA and chromatin immunoprecipitation assays demonstrated that ERR gamma binds to sft4, SF-1RE, and palindromic thyroid hormone response element albeit with different degrees of affinity, but causes hyperacetylation of sft4 and SF-1RE templates only. Limited proteolysis assays showed that ERR gamma, bound to different elements, shows differential trypsin sensitivity. A search for novel coregulators of ERR gamma led to the identification of receptor interacting protein 140 as a potent corepressor and peroxisome proliferator-activated receptor gamma coactivator 1 as a potent coactivator of ERR gamma. DNA-dependent pull-down and transient transfection assays demonstrated that, on different DNA elements, ERR gamma exhibits differential cofactor interactions, which in turn dictate its transcriptional activity. Because ERR gamma shows a similar tissue distribution as peroxisome proliferator-activated receptor gamma coactivator 1 and receptor interacting protein 140, these two coregulators may act as key components of ERR gamma-mediated transcription.

摘要

雌激素受体相关受体γ(ERRγ/ERR3/NR3B3)是ERR亚家族的最新成员,该亚家族还包括ERRα和ERRβ。所有三种异构体都具有高度的氨基酸同一性,尤其是在DNA结合结构域。ERRγ是一种组成型活性转录激活因子,可调节由类固醇生成因子1反应元件(SF-1RE)和雌激素反应元件驱动的报告元件。然而,它对存在于小异二聚体伴侣基因启动子中的SF-1RE衍生物(称为sft4)具有最高的效力,并且与ERRα和-β不同,它无法激活回文甲状腺激素反应元件。为了研究ERRγ这种反应元件特异性差异转录活性背后的机制,监测了ERRγ与上述反应元件的相互作用。电泳迁移率变动分析(EMSA)和染色质免疫沉淀分析表明,ERRγ与sft4、SF-1RE和回文甲状腺激素反应元件结合,尽管亲和力不同,但仅导致sft4和SF-1RE模板的超乙酰化。有限蛋白酶解分析表明,与不同元件结合的ERRγ显示出不同的胰蛋白酶敏感性。对ERRγ新型共调节因子的搜索导致鉴定出受体相互作用蛋白140作为强效共抑制因子,过氧化物酶体增殖物激活受体γ共激活因子1作为ERRγ的强效共激活因子。DNA依赖性下拉和瞬时转染分析表明,在不同的DNA元件上,ERRγ表现出不同的辅因子相互作用,这反过来又决定了其转录活性。由于ERRγ显示出与过氧化物酶体增殖物激活受体γ共激活因子1和受体相互作用蛋白140相似的组织分布,这两种共调节因子可能作为ERRγ介导转录的关键成分。

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