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孤儿核受体ERRγ对转录调控的要求。

Requirements for transcriptional regulation by the orphan nuclear receptor ERRgamma.

作者信息

Huppunen Johanna, Wohlfahrt Gerd, Aarnisalo Piia

机构信息

Biomedicum Helsinki, Institute of Biomedicine, University of Helsinki, P.O. Box 63, FIN-00014 Helsinki, Finland.

出版信息

Mol Cell Endocrinol. 2004 Apr 30;219(1-2):151-60. doi: 10.1016/j.mce.2004.01.002.

Abstract

Estrogen-related receptor gamma (ERRgamma) is an orphan nuclear receptor lacking identified natural ligands. We have addressed the requirements for ERRgamma-mediated gene regulation. ERRgamma transactivates constitutively reporter genes driven by ERR response elements (ERREs) or estrogen response elements (EREs). The activation depends on an intact DNA-binding domain (DBD) and activation function-2 (AF2). ERRgamma-mediated transactivation is further enhanced by peroxisome proliferator-activated receptor coactivator-1. Interestingly, ligand-binding domain (LBD) mutations predicted to either enlarge or diminish the putative ligand-binding pocket have no effect on the transcriptional activity implying that ERRgamma activity does not depend on any ligands. Antiestrogens 4OH-tamoxifen (4OHT) and 4-hydroxytoremifene (4OHtor) inhibit the ability of ERR to transactivate ERRE and ERE reporters. In contrast, ERRgamma activates transcription at AP-1 sites in the presence of 4OHT and 4OHtor. Thus, the transcriptional activity of ERRgamma seems not to require ligand binding but is modulated by binding of certain small synthetic ligands.

摘要

雌激素相关受体γ(ERRγ)是一种缺乏已确定天然配体的孤儿核受体。我们已经研究了ERRγ介导的基因调控的要求。ERRγ组成性地反式激活由ERR反应元件(ERREs)或雌激素反应元件(EREs)驱动的报告基因。这种激活依赖于完整的DNA结合结构域(DBD)和激活功能2(AF2)。ERRγ介导的反式激活通过过氧化物酶体增殖物激活受体辅激活因子-1进一步增强。有趣的是,预测会扩大或缩小假定配体结合口袋的配体结合结构域(LBD)突变对转录活性没有影响,这意味着ERRγ的活性不依赖于任何配体。抗雌激素4-羟基他莫昔芬(4OHT)和4-羟基托瑞米芬(4OHtor)抑制ERR反式激活ERRE和ERE报告基因的能力。相反,在4OHT和4OHtor存在的情况下,ERRγ激活AP-1位点的转录。因此,ERRγ的转录活性似乎不需要配体结合,但受到某些小的合成配体结合的调节。

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