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Gαq与Rho及其交换因子的物理和功能相互作用。

Physical and functional interactions of Galphaq with Rho and its exchange factors.

作者信息

Sagi S A, Seasholtz T M, Kobiashvili M, Wilson B A, Toksoz D, Brown J H

机构信息

Department of Pharmacology, University of California, San Diego, La Jolla, California 92093-0636, USA.

出版信息

J Biol Chem. 2001 May 4;276(18):15445-52. doi: 10.1074/jbc.M008961200. Epub 2001 Feb 6.

Abstract

Recent reports have shown that several heterotrimeric protein-coupled receptors that signal through Galpha(q) can induce Rho-dependent responses, but the pathways that mediate the interaction between Galpha(q) and Rho have not yet been identified. In this report we present evidence that Galpha(q) expressed in COS-7 cells coprecipitates with the Rho guanine nucleotide exchange factor (GEF) Lbc. Furthermore, Galpha(q) expression enhances Rho-dependent responses. Coexpressed Galpha(q) and Lbc have a synergistic effect on the Rho-dependent rounding of 1321N1 astrocytoma cells. In addition, serum response factor-dependent gene expression, as assessed by the SRE.L reporter gene, is synergistically activated by Galpha(q) and Rho GEFs. The synergistic effect of Galpha(q) on this response is inhibited by C3 exoenzyme and requires phospholipase C activation. Surprisingly, expression of Galpha(q), in contrast to that of Galpha(12) and Galpha(13), does not increase the amount of activated Rho. We also observe that Galpha(q) enhances SRE.L stimulation by activated Rho, indicating that the effect of Galpha(q) occurs downstream of Rho activation. Thus, Galpha(q) interacts physically and/or functionally with Rho GEFs; however this does not appear to lead to or result from increased activation of Rho. We suggest that Galpha(q)-generated signals enhance responses downstream of Rho activation.

摘要

最近的报告显示,几种通过Gαq信号传导的异源三聚体蛋白偶联受体可诱导Rho依赖性反应,但介导Gαq与Rho相互作用的途径尚未明确。在本报告中,我们提供证据表明,在COS-7细胞中表达的Gαq与Rho鸟嘌呤核苷酸交换因子(GEF)Lbc共沉淀。此外,Gαq的表达增强了Rho依赖性反应。共表达的Gαq和Lbc对1321N1星形细胞瘤细胞的Rho依赖性变圆具有协同作用。此外,通过SRE.L报告基因评估的血清反应因子依赖性基因表达被Gαq和Rho GEF协同激活。Gαq对该反应的协同作用被C3外切酶抑制,并且需要磷脂酶C激活。令人惊讶的是,与Gα12和Gα13相比,Gαq的表达不会增加活化Rho的量。我们还观察到Gαq增强了活化Rho对SRE.L的刺激,表明Gαq的作用发生在Rho激活的下游。因此,Gαq与Rho GEF在物理和/或功能上相互作用;然而,这似乎不会导致Rho活化增加,也不是由Rho活化增加引起的。我们认为,Gαq产生的信号增强了Rho激活下游的反应。

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Regulation of SRF activity by Rho family GTPases.
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