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G 蛋白偶联受体向翻译机器的信号转导。

GPCR signalling to the translation machinery.

机构信息

BIOS group, INRA, UMR, Unité Physiologie de la Reproduction et des Comportements, Nouzilly, France.

出版信息

Cell Signal. 2010 May;22(5):707-16. doi: 10.1016/j.cellsig.2009.10.012. Epub 2009 Oct 31.

Abstract

G protein-coupled receptors (GPCRs) are involved in most physiological processes, many of them being engaged in fully differentiated cells. These receptors couple to transducers of their own, primarily G proteins and beta-arrestins, which launch intracellular signalling cascades. Some of these signalling events regulate the translational machinery to fine-tune general cell metabolism or to alter protein expression pattern. Though extensively documented for tyrosine kinase receptors, translational regulation by GPCRs is still poorly appreciated. The objective of this review paper is to address the following questions: i) is there a "GPCR signature" impacting on the translational machinery, and ultimately on the type of mRNA translated? ii) are the regulatory networks involved similar as those utilized by tyrosine kinase receptors? In particular, we will discuss the specific features of translational control mediated by GPCRs and highlight the intrinsic properties of GPCRs these mechanisms could rely on.

摘要

G 蛋白偶联受体 (GPCRs) 参与大多数生理过程,其中许多受体与完全分化的细胞结合。这些受体与自身的转导器结合,主要是 G 蛋白和β-arrestin,它们启动细胞内信号级联反应。这些信号事件中的一些调节翻译机制,以微调一般细胞代谢或改变蛋白质表达模式。尽管酪氨酸激酶受体的翻译调控已经得到广泛的研究,但 GPCR 的翻译调控仍然知之甚少。本文的目的是探讨以下问题:i)是否存在影响翻译机制,最终影响翻译 mRNA 类型的“GPCR 特征”?ii)涉及的调控网络是否与酪氨酸激酶受体相同?特别是,我们将讨论 GPCR 介导的翻译控制的特定特征,并强调这些机制可能依赖的 GPCR 的内在特性。

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