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酿酒酵母CDC24和CDC42之间功能相互作用的遗传证据。

Genetic evidence for a functional interaction between Saccharomyces cerevisiae CDC24 and CDC42.

作者信息

Ziman M, Johnson D I

机构信息

Department of Microbiology and Molecular Genetics, University of Vermont, Burlington 05401.

出版信息

Yeast. 1994 Apr;10(4):463-74. doi: 10.1002/yea.320100405.

Abstract

Cdc24p and Cdc42p are involved in the control of cell polarity during the Saccharomyces cerevisiae cell cycle. Cdc42p is a member of the Ras superfamily of GTPases and Cdc24p displays limited amino-acid sequence similarity with the Dbl proto-oncoprotein, which acts to stimulate guanine-nucleotide exchange on human Cdc42p. We have performed several genetic experiments to test whether Cdc24p and Cdc42p interact within the cell. First, overexpression of Cdc24p suppressed the dominant-negative cdc42D118A allele. Second, overexpression of wild-type CDC24 and CDC42 genes together was a lethal event resulting in a morphological phenotype of large, round, unbudded cells, indicating a loss of cell polarity. Third, a cdc24ts cdc42ts double mutant exhibited a synthetic-lethal phenotype at the semi-permissive temperature of 30 degrees C. These data suggest that Cdc24p and Cdc42p interact within the cell and that Cdc24p may be involved in the regulation of Cdc42p activity.

摘要

Cdc24p和Cdc42p参与酿酒酵母细胞周期中细胞极性的控制。Cdc42p是GTP酶Ras超家族的成员,Cdc24p与Dbl原癌蛋白的氨基酸序列相似性有限,Dbl原癌蛋白可刺激人Cdc42p上的鸟嘌呤核苷酸交换。我们进行了多项遗传学实验,以测试Cdc24p和Cdc42p在细胞内是否相互作用。首先,Cdc24p的过表达抑制了显性负性cdc42D118A等位基因。其次,野生型CDC24和CDC42基因一起过表达是一个致死事件,导致出现大的、圆形的、未出芽细胞的形态学表型,表明细胞极性丧失。第三,cdc24ts cdc42ts双突变体在30摄氏度的半允许温度下表现出合成致死表型。这些数据表明Cdc24p和Cdc42p在细胞内相互作用,并且Cdc24p可能参与Cdc42p活性的调节。

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