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酵母rad18突变体特异性地增加了G.C到T.A的颠换,而不会降低G-A或C-T错配到G.C对的校正。

The yeast rad18 mutator specifically increases G.C----T.A transversions without reducing correction of G-A or C-T mismatches to G.C pairs.

作者信息

Kunz B A, Kang X L, Kohalmi L

机构信息

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

出版信息

Mol Cell Biol. 1991 Jan;11(1):218-25. doi: 10.1128/mcb.11.1.218-225.1991.

Abstract

Inactivation of the Saccharomyces cerevisiae RAD18 gene confers a mutator phenotype. To determine the specificity of this effect, a collection of 212 spontaneous SUP4-o mutants arising in a rad18 strain was characterized by DNA sequencing. Comparison of the resulting mutational spectrum with that for an isogenic wild-type (RAD18) strain revealed that the rad18 mutator specifically enhanced the frequency of single base pair substitutions. Further analysis indicated that an increase in the frequency of G.C----T.A transversions accounted for the elevated SUP4-o mutation frequency. Thus, rad18 is the first eucaryotic mutator found to generate only a particular base pair substitution. The majority of G.C pairs that were not mutated in the rad18 background were at sites where G.C----T.A events can be detected in SUP4-o, suggesting that DNA sequence context influences the rad18 mutator effect. Transformation of heteroduplex plasmid DNAs into the two strains demonstrated that the rad18 mutator did not reduce the efficiency of correcting G-A or C-T mismatches to G.C pairs or preferentially correct the mismatches to A.T pairs. We propose that the RAD18 gene product might contribute to the fidelity of DNA replication in S. cerevisiae by involvement in a process that serves to limit the formation of G-A and C-T mismatches at template guanine and cytosine sites during DNA synthesis.

摘要

酿酒酵母RAD18基因的失活赋予了一种突变体表型。为了确定这种效应的特异性,通过DNA测序对在rad18菌株中产生的212个自发SUP4-o突变体进行了表征。将所得突变谱与同基因野生型(RAD18)菌株的突变谱进行比较,发现rad18突变体特异性地提高了单碱基对替换的频率。进一步分析表明,G.C----T.A颠换频率的增加导致了SUP4-o突变频率的升高。因此,rad18是第一个被发现仅产生特定碱基对替换的真核突变体。在rad18背景中未发生突变的大多数G.C对位于在SUP4-o中可检测到G.C----T.A事件的位点,这表明DNA序列背景影响rad18突变体效应。将异源双链体质粒DNA转化到这两种菌株中表明,rad18突变体不会降低将G-A或C-T错配校正为G.C对的效率,也不会优先将错配校正为A.T对。我们提出,RAD18基因产物可能通过参与一个在DNA合成过程中限制模板鸟嘌呤和胞嘧啶位点处G-A和C-T错配形成的过程,对酿酒酵母中DNA复制的保真度做出贡献。

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