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酿酒酵母rad6、rad18和rad52突变体的特异性表现出对REV3基因产物(一种假定的非必需DNA聚合酶)不同程度的依赖性。

Specificities of the Saccharomyces cerevisiae rad6, rad18, and rad52 mutators exhibit different degrees of dependence on the REV3 gene product, a putative nonessential DNA polymerase.

作者信息

Roche H, Gietz R D, Kunz B A

机构信息

Department of Microbiology, University of Manitoba, Winnipeg, Canada.

出版信息

Genetics. 1995 Jun;140(2):443-56. doi: 10.1093/genetics/140.2.443.

Abstract

The Saccharomyces cerevisiae rad6, rad18, and rad52 mutants exhibit DNA repair deficiencies and distinct mutator phenotypes. DNA replication past unrepaired spontaneous damage might contribute to the specificities of these mutators. Because REV3 is thought to encode a DNA polymerase that specializes in translesion synthesis, we determined the REV3 dependence of the rad mutator specificities. Spontaneous mutagenesis at a plasmid-borne SUP4-o locus was examined in isogenic strains having combinations of normal or mutant REV3 and RAD6, RAD18, or RAD52 alleles. For the rad6 and rad18 mutators, the mutation rate increase relied largely, but not exclusively, on REV3 whereas the rad52 mutator was entirely REV3 dependent. The influence of REV3 on the specificity of the rad6 mutator differed markedly depending on the mutational class examined. However, the requirement of rev3 for the production of G.C-->T.A transversions by the rad18 mutator, which induces only these substitutions, was similar to that for rad6-mediated G.C-->T.A transversion. This supports a role for the Rad6-Rad18 protein complex in the control of spontaneous mutagenesis. The available data imply that the putative Rev3 polymerase can process a variety of spontaneous DNA lesions that normally are substrates for error-free repair.

摘要

酿酒酵母的rad6、rad18和rad52突变体表现出DNA修复缺陷和不同的突变表型。绕过未修复的自发损伤进行DNA复制可能导致这些突变体产生特异性。由于REV3被认为编码一种专门负责跨损伤合成的DNA聚合酶,我们确定了rad突变体特异性对REV3的依赖性。在具有正常或突变REV3与RAD6、RAD18或RAD52等位基因组合的同基因菌株中,检测了质粒携带的SUP4-o位点的自发诱变情况。对于rad6和rad18突变体,突变率的增加在很大程度上但并非完全依赖于REV3,而rad52突变体则完全依赖于REV3。REV3对rad6突变体特异性的影响根据所检测的突变类别而有显著差异。然而,rev3对于由仅诱导这些替换的rad18突变体产生G.C→T.A颠换的需求,与rad6介导的G.C→T.A颠换相似。这支持了Rad6-Rad18蛋白复合物在控制自发诱变中的作用。现有数据表明,假定的Rev3聚合酶可以处理多种通常是无错修复底物的自发DNA损伤。

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