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类固醇受体异二聚化在体外和体内均得到证实。

Steroid receptor heterodimerization demonstrated in vitro and in vivo.

作者信息

Liu W, Wang J, Sauter N K, Pearce D

机构信息

Department of Medicine, San Francisco General Hospital, CA, USA.

出版信息

Proc Natl Acad Sci U S A. 1995 Dec 19;92(26):12480-4. doi: 10.1073/pnas.92.26.12480.

Abstract

The mineralocorticoid and glucocorticoid receptors (MR and GR, respectively) are members of the intracellular receptor superfamily that bind as homodimers to the same hormone response elements (HREs). Physiological evidence suggests that MR and GR interact with each other in cells that express both receptors, implying that they might directly interact in the regulation of transcription initiation. Indeed, we have found that coexpressed MR and GR interact functionally at the transcriptional level and furthermore that they interact physically through heterodimer formation at a shared HRE in vitro and in vivo. We suggest from these findings that heterodimerization may play an important role in steroid receptor transcriptional regulation.

摘要

盐皮质激素受体和糖皮质激素受体(分别为MR和GR)是细胞内受体超家族的成员,它们作为同二聚体与相同的激素反应元件(HRE)结合。生理学证据表明,在同时表达这两种受体的细胞中,MR和GR会相互作用,这意味着它们可能在转录起始调控中直接相互作用。事实上,我们发现共表达的MR和GR在转录水平上有功能相互作用,而且它们在体外和体内通过在共享的HRE处形成异二聚体而发生物理相互作用。基于这些发现,我们认为异二聚化可能在类固醇受体转录调控中发挥重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7378/40381/8aaf0a582033/pnas01504-0545-a.jpg

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