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哺乳动物Gα及哺乳动物-酵母杂交Gα蛋白的表达对酵母信息素反应信号转导途径的影响。

Effects of expression of mammalian G alpha and hybrid mammalian-yeast G alpha proteins on the yeast pheromone response signal transduction pathway.

作者信息

Kang Y S, Kane J, Kurjan J, Stadel J M, Tipper D J

机构信息

Department of Molecular Genetics and Microbiology, University of Massachusetts Medical Center, Worcester 01655.

出版信息

Mol Cell Biol. 1990 Jun;10(6):2582-90. doi: 10.1128/mcb.10.6.2582-2590.1990.

DOI:10.1128/mcb.10.6.2582-2590.1990
PMID:2111439
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC360616/
Abstract

Scg1, the product of the Saccharomyces cerevisiae SCG1 (also called GPA1) gene, is homologous to the alpha subunits of G proteins involved in signal transduction in mammalian cells. Scg1 negatively controls the pheromone response pathway in haploid cells. Either pheromonal activation or an scg1 null mutation relieves the negative control and leads to an arrest of cell growth in the G1 phase of the cell cycle. Expression of rat G alpha s was previously shown to complement the growth defect of scg1 null mutants while not allowing mating. We have extended this analysis to examine the effects of the short form of G alpha s (which lacks 15 amino acids present in the long form), G alpha i2, G alpha o, and Scg1-mammalian G alpha hybrids. In addition, we have found that constructs able to complement scg1 are also able to inhibit the response to pheromone and mating when expressed in a wild-type SCG1 strain. Overexpression of Scg1 has a similar inhibitory effect. These results are consistent with a model proposed for the action of Scg1 as the alpha component of a heterotrimeric G protein in which the beta gamma component (Ste4/Ste18) activates the pheromone response after dissociation from Scg1. They suggest that the G alpha constructs able to complement scg1 can interact with beta gamma to prevent activation of the pathway but are unable to interact with pheromone receptors to activate the pathway.

摘要

Scg1是酿酒酵母SCG1(也称为GPA1)基因的产物,与参与哺乳动物细胞信号转导的G蛋白α亚基同源。Scg1对单倍体细胞中的信息素反应途径起负调控作用。信息素激活或scg1缺失突变均可解除负调控,并导致细胞周期G1期细胞生长停滞。先前的研究表明,大鼠Gαs的表达可弥补scg1缺失突变体的生长缺陷,但不允许细胞交配。我们扩展了这项分析,以研究短形式的Gαs(缺少长形式中存在的15个氨基酸)、Gαi2、Gαo以及Scg1-哺乳动物Gα杂种的作用。此外,我们发现能够弥补scg1的构建体在野生型SCG1菌株中表达时,也能够抑制对信息素的反应和细胞交配。Scg1的过表达具有类似的抑制作用。这些结果与提出的Scg1作为异源三聚体G蛋白α亚基作用的模型一致,其中βγ亚基(Ste4/Ste18)从Scg1解离后激活信息素反应途径。这表明能够弥补scg1的Gα构建体可以与βγ相互作用以阻止途径的激活,但不能与信息素受体相互作用以激活途径。

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