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RACK1调节Gβγ的特定功能。

RACK1 regulates specific functions of Gbetagamma.

作者信息

Chen Songhai, Dell Edward J, Lin Fang, Sai Jiqing, Hamm Heidi E

机构信息

Department of Pharmacology, Vanderbilt University Medical Center, Nashville, Tennessee 37232-6600, USA.

出版信息

J Biol Chem. 2004 Apr 23;279(17):17861-8. doi: 10.1074/jbc.M313727200. Epub 2004 Feb 12.

Abstract

We showed previously that Gbetagamma interacts with Receptor for Activated C Kinase 1 (RACK1), a protein that not only binds activated protein kinase C (PKC) but also serves as an adaptor/scaffold for many signaling pathways. Here we report that RACK1 does not interact with Galpha subunits or heterotrimeric G proteins but binds free Gbetagamma subunits released from activated heterotrimeric G proteins following the activation of their cognate receptors in vivo. The association with Gbetagamma promotes the translocation of RACK1 from the cytosol to the membrane. Moreover, binding of RACK1 to Gbetagamma results in inhibition of Gbetagamma-mediated activation of phospholipase C beta2 and adenylyl cyclase II. However, RACK1 has no effect on other functions of Gbetagamma, such as activation of the mitogen-activated protein kinase signaling pathway or chemotaxis of HEK293 cells via the chemokine receptor CXCR2. Similarly, RACK1 does not affect signal transduction through the Galpha subunits of G(i), G(s), or G(q). Collectively, these findings suggest a role of RACK1 in regulating specific functions of Gbetagamma.

摘要

我们之前发现,Gβγ与活化C激酶1受体(RACK1)相互作用,RACK1不仅能结合活化的蛋白激酶C(PKC),还作为许多信号通路的衔接蛋白/支架蛋白。在此我们报告,RACK1不与Gα亚基或异源三聚体G蛋白相互作用,而是在体内同源受体激活后,与从活化的异源三聚体G蛋白释放的游离Gβγ亚基结合。与Gβγ的结合促进RACK1从胞质溶胶向细胞膜的转位。此外,RACK1与Gβγ的结合导致Gβγ介导的磷脂酶Cβ2和腺苷酸环化酶II的激活受到抑制。然而,RACK1对Gβγ的其他功能没有影响,如丝裂原活化蛋白激酶信号通路的激活或通过趋化因子受体CXCR2介导的HEK293细胞趋化性。同样,RACK1不影响通过G(i)、G(s)或G(q)的Gα亚基进行的信号转导。这些发现共同表明RACK1在调节Gβγ的特定功能中发挥作用。

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