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酿酒酵母RAD6蛋白中半胱氨酸88的突变消除了其泛素结合活性及其各种生物学功能。

Mutation of cysteine-88 in the Saccharomyces cerevisiae RAD6 protein abolishes its ubiquitin-conjugating activity and its various biological functions.

作者信息

Sung P, Prakash S, Prakash L

机构信息

Department of Biology, University of Rochester, NY 14627.

出版信息

Proc Natl Acad Sci U S A. 1990 Apr;87(7):2695-9. doi: 10.1073/pnas.87.7.2695.

Abstract

The RAD6 gene of Saccharomyces cerevisiae is required for DNA repair, DNA damage-induced mutagenesis, and sporulation. RAD6 protein is a ubiquitin-conjugating enzyme (E2) that has been shown to attach multiple molecules of ubiquitin to histones H2A and H2B. We have now examined whether the E2 activity of RAD6 is involved in its various biological functions. Since the formation of a thioester adduct between E2 and ubiquitin is necessary for E2 activity, the single cysteine residue (Cys-88) present in RAD6 was changed to alanine or valine. The mutant proteins were overproduced in yeast cells and purified to near homogeneity. We show that the rad6 Ala-88 and rad6 Val-88 mutant proteins lack the capacity for thioester formation with ubiquitin and, as a consequence, are totally devoid of any E2 activity. The rad6 Ala-88 and rad6 Val-88 mutations confer a defect in DNA repair, mutagenesis, and sporulation equivalent to that in the rad6 null allele. We suggest that the biological functions of RAD6 require its E2 activity.

摘要

酿酒酵母的RAD6基因对于DNA修复、DNA损伤诱导的诱变以及孢子形成是必需的。RAD6蛋白是一种泛素结合酶(E2),已证明它能将多个泛素分子连接到组蛋白H2A和H2B上。我们现在研究了RAD6的E2活性是否参与其各种生物学功能。由于E2和泛素之间硫酯加合物的形成对于E2活性是必需的,因此将RAD6中存在的单个半胱氨酸残基(Cys-88)替换为丙氨酸或缬氨酸。突变蛋白在酵母细胞中过量表达并纯化至接近均一。我们表明,rad6 Ala-88和rad6 Val-88突变蛋白缺乏与泛素形成硫酯的能力,因此完全没有任何E2活性。rad6 Ala-88和rad6 Val-88突变导致DNA修复、诱变和孢子形成缺陷,等同于rad6无效等位基因中的缺陷。我们认为RAD6的生物学功能需要其E2活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0d9c/53757/4d7c87d978b7/pnas01032-0323-a.jpg

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