Estrogen-related receptor β (ERRβ) - renaissance receptor or receptor renaissance?

Nuclear receptor signaling Pub Date : 2016-06-21 eCollection Date: 2016-01-01 DOI:10.1621/nrs.14002
Shailaja D Divekar, Deanna M Tiek, Aileen Fernandez, Rebecca B Riggins
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引用次数: 26

Abstract

Estrogen-related receptors (ERRs) are founding members of the orphan nuclear receptor (ONR) subgroup of the nuclear receptor superfamily. Twenty-seven years of study have yet to identify cognate ligands for the ERRs, though they have firmly placed ERRα and ERRγ at the intersection of cellular metabolism and oncogenesis. The pace of discovery for novel functions of ERRβ, however, has until recently been somewhat slower than that of its family members. ERRβ has also been largely ignored in summaries and perspectives of the ONR literature. Here, we provide an overview of established and emerging knowledge of ERRβ in mouse, man, and other species, highlighting unique aspects of ERRβ biology that set it apart from the other two estrogen-related receptors, with a focus on the impact of alternative splicing on the structure and function of this receptor.

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雌激素相关受体β (ERRβ) -受体复兴还是受体复兴?
雌激素相关受体(ERRs)是核受体超家族孤儿核受体(ONR)亚群的创始成员。27年的研究尚未确定ERRs的同源配体,尽管他们已经坚定地将ERRα和ERRγ置于细胞代谢和肿瘤发生的交叉点。然而,直到最近,ERRβ新功能的发现速度比它的家族成员要慢一些。在ONR文献的总结和观点中,ERRβ也在很大程度上被忽略了。在这里,我们概述了小鼠、人类和其他物种中ERRβ的现有和新兴知识,强调了ERRβ生物学的独特方面,将其与其他两种雌激素相关受体区分开来,重点关注了选择性剪接对该受体结构和功能的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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