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Gα12通过小G蛋白Ras和Rac刺激c-Jun氨基末端激酶。

Galpha12 stimulates c-Jun NH2-terminal kinase through the small G proteins Ras and Rac.

作者信息

Collins L R, Minden A, Karin M, Brown J H

机构信息

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

出版信息

J Biol Chem. 1996 Jul 19;271(29):17349-53. doi: 10.1074/jbc.271.29.17349.

Abstract

The pertussis toxin (PTX) insensitive heterotrimeric G protein G12 has been implicated in mitogenesis and transformation, but its direct effectors remain unknown. To define potential signaling pathways utilized by G12, we expressed an activated mutant of its alpha subunit, Galpha12(Q229L), in HEK293 cells and examined its effects on Ras and mitogen-activated protein kinases (MAPKs). Transient expression of activated Galpha12 increased the percentage of Ras in the active, GTP-bound state, stimulated c-Jun NH2-terminal kinase (JNK) activity, and enhanced the transcriptional activity of c-Jun. Dominant negative Ras (N17Ras) inhibited Galpha12-mediated JNK activation in NIH3T3 cells but failed to do so in HEK293 cells. In contrast, dominant negative Rac (N17Rac1) inhibited JNK activation by Galpha12 in HEK293 cells as well as three other cell lines. In 1321N1 cells, where thrombin stimulates G12-dependent mitogenesis, coexpression of N17Rac1 or a dominant negative mutant of MEKK1 (MEKKDelta(K432M)) inhibits c-Jun/AP-1 sensitive reporter gene expression stimulated by thrombin or Galpha12. These data demonstrate that the alpha subunit of the heterotrimeric G protein G12, like tyrosine kinase growth factor receptors, activates Ras and recruits a signal transduction pathway involving the small GTP-binding protein Rac that leads to JNK activation.

摘要

百日咳毒素(PTX)不敏感的异源三聚体G蛋白G12与有丝分裂和细胞转化有关,但其直接效应器仍不清楚。为了确定G12利用的潜在信号通路,我们在HEK293细胞中表达了其α亚基Gα12(Q229L)的活化突变体,并研究了其对Ras和丝裂原活化蛋白激酶(MAPK)的影响。活化的Gα12的瞬时表达增加了处于活性、GTP结合状态的Ras的百分比,刺激了c-Jun氨基末端激酶(JNK)的活性,并增强了c-Jun的转录活性。显性负性Ras(N17Ras)在NIH3T3细胞中抑制Gα12介导的JNK活化,但在HEK293细胞中未能抑制。相反,显性负性Rac(N17Rac1)在HEK293细胞以及其他三种细胞系中抑制Gα12对JNK的活化。在凝血酶刺激G12依赖性有丝分裂的1321N1细胞中,N17Rac1或MEKK1的显性负性突变体(MEKKΔ(K432M))的共表达抑制了凝血酶或Gα12刺激的c-Jun/AP-1敏感报告基因的表达。这些数据表明,异源三聚体G蛋白G12的α亚基与酪氨酸激酶生长因子受体一样,激活Ras并募集一条涉及小GTP结合蛋白Rac的信号转导通路,该通路导致JNK活化。

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