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异常复制诱导的突变体表型

Mutator phenotype induced by aberrant replication.

作者信息

Liu V F, Bhaumik D, Wang T S

机构信息

Department of Pathology, Stanford University School of Medicine, Stanford, California 94305-5324, USA.

出版信息

Mol Cell Biol. 1999 Feb;19(2):1126-35. doi: 10.1128/MCB.19.2.1126.

Abstract

We have identified thermosensitive mutants of five Schizosaccharomyces pombe replication proteins that have a mutator phenotype at their semipermissive temperatures. Allele-specific mutants of DNA polymerase delta (poldelta) and mutants of Polalpha, two Poldelta subunits, and ligase exhibited increased rates of deletion of sequences flanked by short direct repeats. Deletion of rad2(+), which encodes a nuclease involved in processing Okazaki fragments, caused an increased rate of duplication of sequences flanked by short direct repeats. The deletion mutation rates of all the thermosensitive replication mutators decreased in a rad2Delta background, suggesting that deletion formation requires Rad2 function. The duplication mutation rate of rad2Delta was also reduced in a thermosensitive polymerase background, but not in a ligase mutator background, which suggests that formation of duplication mutations requires normal DNA polymerization. Thus, although the deletion and duplication mutator phenotypes are distinct, their mutational mechanisms are interdependent. The deletion and duplication replication mutators all exhibited decreased viability in combination with deletion of a checkpoint Rad protein, Rad26. Interestingly, deletion of Cds1, a protein kinase functioning in a checkpoint Rad-mediated reversible S-phase arrest pathway, decreased the viability and exacerbated the mutation rate only in the thermosensitive deletion replication mutators but had no effect on rad2Delta. These findings suggest that aberrant replication caused by allele-specific mutations of these replication proteins can accumulate potentially mutagenic DNA structures. The checkpoint Rad-mediated pathways monitor and signal the aberrant replication in both the deletion and duplication mutators, while Cds1 mediates recovery from aberrant replication and prevents formation of deletion mutations specifically in the thermosensitive deletion replication mutators.

摘要

我们已经鉴定出五种粟酒裂殖酵母复制蛋白的温度敏感突变体,它们在半允许温度下具有诱变表型。DNA聚合酶δ(Poldelta)的等位基因特异性突变体以及Polalpha、两个Poldelta亚基和连接酶的突变体,表现出短直接重复序列侧翼序列缺失率增加。编码参与冈崎片段加工的核酸酶的rad2(+)缺失,导致短直接重复序列侧翼序列的重复率增加。所有温度敏感复制诱变剂的缺失突变率在rad2Delta背景下均降低,这表明缺失的形成需要Rad2功能。rad2Delta的重复突变率在温度敏感聚合酶背景下也降低,但在连接酶诱变剂背景下未降低,这表明重复突变的形成需要正常的DNA聚合作用。因此,尽管缺失和重复诱变表型不同,但其突变机制相互依赖。缺失和重复复制诱变剂与检查点Rad蛋白Rad26的缺失相结合时,均表现出活力降低。有趣的是,在检查点Rad介导的可逆S期停滞途径中起作用的蛋白激酶Cds1的缺失,仅在温度敏感缺失复制诱变剂中降低了活力并加剧了突变率,但对rad2Delta没有影响。这些发现表明,这些复制蛋白的等位基因特异性突变导致的异常复制会积累潜在的诱变DNA结构。检查点Rad介导的途径监测并发出缺失和重复诱变剂中异常复制的信号,而Cds1介导从异常复制中恢复,并特别防止在温度敏感缺失复制诱变剂中形成缺失突变。

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