Department of Biochemistry, Emory University School of Medicine, Atlanta, GA 30322, U.S.A.
Biochem Soc Trans. 2021 Nov 1;49(5):2333-2343. doi: 10.1042/BST20210419.
The glucocorticoid receptor (GR) is a steroid hormone-activated transcription factor that binds to various glucocorticoid response elements to up- or down- regulate the transcription of thousands of genes involved in metabolism, development, stress and inflammatory responses. GR consists of two domains enabling interaction with glucocorticoids, DNA response elements and coregulators, as well as a large intrinsically disordered region that mediates condensate formation. A growing body of structural studies during the past decade have shed new light on GR interactions, providing a new understanding of the mechanisms driving context-specific GR activity. Here, we summarize the established and emerging mechanisms of action of GR, primarily from a structural perspective. This minireview also discusses how the current state of knowledge of GR function may guide future glucocorticoid design with an improved therapeutic index for different inflammatory disorders.
糖皮质激素受体 (GR) 是一种甾体激素激活的转录因子,可与各种糖皮质激素反应元件结合,上调或下调参与代谢、发育、应激和炎症反应的数千个基因的转录。GR 由两个结构域组成,这两个结构域使 GR 能够与糖皮质激素、DNA 反应元件和共激活因子相互作用,以及一个介导凝聚物形成的大型固有无序区域。在过去十年中,越来越多的结构研究为 GR 相互作用提供了新的见解,为驱动特定于上下文的 GR 活性的机制提供了新的认识。在这里,我们主要从结构角度总结了 GR 的既定和新兴作用机制。这篇迷你评论还讨论了 GR 功能的现有知识状态如何为不同炎症性疾病的糖皮质激素设计提供指导,以提高治疗指数。