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GPR158/179 通过控制 RGS7 复合物的定位和活性来调节 G 蛋白信号转导。

GPR158/179 regulate G protein signaling by controlling localization and activity of the RGS7 complexes.

机构信息

Department of Neuroscience, The Scripps Research Institute, Jupiter, FL 33458, USA.

出版信息

J Cell Biol. 2012 Jun 11;197(6):711-9. doi: 10.1083/jcb.201202123.

Abstract

The extent and temporal characteristics of G protein-coupled receptor (GPCR) signaling are shaped by the regulator of G protein signaling (RGS) proteins, which promote G protein deactivation. With hundreds of GPCRs and dozens of RGS proteins, compartmentalization plays a key role in establishing signaling specificity. However, the molecular details and mechanisms of this process are poorly understood. In this paper, we report that the R7 group of RGS regulators is controlled by interaction with two previously uncharacterized orphan GPCRs: GPR158 and GPR179. We show that GPR158/179 recruited RGS complexes to the plasma membrane and augmented their ability to regulate GPCR signaling. The loss of GPR179 in a mouse model of night blindness prevented targeting of RGS to the postsynaptic compartment of bipolar neurons in the retina, illuminating the role of GPR179 in night vision. We propose that the interaction of RGS proteins with orphan GPCRs promotes signaling selectivity in G protein pathways.

摘要

G 蛋白偶联受体(GPCR)信号的范围和时变特征受 G 蛋白信号调节因子(RGS)蛋白的调控,这些蛋白促进 G 蛋白失活。有数百种 GPCR 和数十种 RGS 蛋白,区室化在建立信号特异性方面起着关键作用。然而,这一过程的分子细节和机制还知之甚少。在本文中,我们报告说,R7 组 RGS 调节剂受与两个以前未表征的孤儿 GPCR(GPR158 和 GPR179)相互作用的控制。我们表明,GPR158/179 将 RGS 复合物募集到质膜,并增强了它们调节 GPCR 信号的能力。在夜盲症的小鼠模型中缺失 GPR179 会阻止 RGS 靶向视网膜双极神经元的突触后隔室,阐明了 GPR179 在夜视中的作用。我们提出,RGS 蛋白与孤儿 GPCR 的相互作用促进了 G 蛋白途径中信号的选择性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4a7d/3373406/b6195d58d3e6/JCB_201202123_Fig1.jpg

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