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β1肾上腺素能受体与环磷酸腺苷依赖性鸟嘌呤核苷酸交换因子CNrasGEF的直接结合导致Ras激活。

Direct binding of the beta1 adrenergic receptor to the cyclic AMP-dependent guanine nucleotide exchange factor CNrasGEF leads to Ras activation.

作者信息

Pak Youngshil, Pham Nam, Rotin Daniela

机构信息

Program in Cell Biology, The Hospital for Sick Children, and Biochemistry Department, University of Toronto, Toronto, M5G 1X8 Ontario, Canada.

出版信息

Mol Cell Biol. 2002 Nov;22(22):7942-52. doi: 10.1128/MCB.22.22.7942-7952.2002.

Abstract

G-protein-coupled receptors (GPCRs) can indirectly activate Ras primarily through the betagamma subunits of G proteins, which recruit c-Src, phosphatidylinositol 3-kinase, and Grb2-SOS. However, a direct interaction between a Ras activator (guanine nucleotide exchange factor [GEF]) and GPCRs that leads to Ras activation has never been demonstrated. We report here a novel mechanism for a direct GPCR-mediated Ras activation. The beta1 adrenergic receptor (beta1-AR) binds to the PDZ domain of the cyclic AMP (cAMP)-dependent Ras exchange factor, CNrasGEF, via its C-terminal SkV motif. In cells heterologously expressing beta1-AR and CNrasGEF, Ras is activated by the beta1-AR agonist isoproterenol, and this activation is abolished in beta1-AR mutants that cannot bind CNrasGEF or in CNrasGEF mutants lacking the catalytic CDC25 domain or cAMP-binding domain. Moreover, the activation is transduced via Gsalpha and not via Gbetagamma. In contrast to beta1-AR, the beta2-AR neither binds CNrasGEF nor activates Ras via CNrasGEF after agonist stimulation. These results suggest a model whereby the physical interaction between the beta1-AR and CNrasGEF facilitates the transduction of Gsalpha-induced cAMP signal into the activation of Ras. The present study provides the first demonstration of direct physical association between a Ras activator and a GPCR, leading to agonist-induced Ras activation

摘要

G蛋白偶联受体(GPCRs)主要通过G蛋白的βγ亚基间接激活Ras,βγ亚基可募集c-Src、磷脂酰肌醇3激酶和Grb2-SOS。然而,从未证实过Ras激活剂(鸟嘌呤核苷酸交换因子[GEF])与GPCRs之间存在直接相互作用并导致Ras激活。我们在此报告一种由GPCR直接介导Ras激活的新机制。β1肾上腺素能受体(β1-AR)通过其C端SkV基序与环磷酸腺苷(cAMP)依赖性Ras交换因子CNrasGEF的PDZ结构域结合。在异源表达β1-AR和CNrasGEF的细胞中,β1-AR激动剂异丙肾上腺素可激活Ras,而在无法结合CNrasGEF的β1-AR突变体或缺乏催化性CDC25结构域或cAMP结合结构域的CNrasGEF突变体中,这种激活作用消失。此外,激活作用是通过Gsα转导的,而非通过Gβγ。与β1-AR不同,β2-AR在激动剂刺激后既不结合CNrasGEF,也不通过CNrasGEF激活Ras。这些结果提示了一种模型,即β1-AR与CNrasGEF之间的物理相互作用有助于将Gsα诱导的cAMP信号转导为Ras激活。本研究首次证明了Ras激活剂与GPCR之间存在直接物理关联,从而导致激动剂诱导的Ras激活。

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