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粟酒裂殖酵母rad26的一个新型突变等位基因在监测S期进程以防止过早有丝分裂方面存在缺陷。

A novel mutant allele of Schizosaccharomyces pombe rad26 defective in monitoring S-phase progression to prevent premature mitosis.

作者信息

Uchiyama M, Galli I, Griffiths D J, Wang T S

机构信息

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

出版信息

Mol Cell Biol. 1997 Jun;17(6):3103-15. doi: 10.1128/MCB.17.6.3103.

Abstract

A semipermissive growth condition was defined for a Schizosaccharomyces pombe strain carrying a thermosensitive allele of DNA polymerase delta (pol delta ts03). Under this condition, DNA polymerase delta is semidisabled and causes a delay in S-phase progression. Using a genetic strategy, we have isolated a panel of mutants that enter premature mitosis when DNA replication is incomplete but which are not defective for arrest in G2/M following DNA damage. We characterized the aya14 mutant, which enters premature mitosis when S phase is arrested by genetic or chemical means. However, this mutant is sensitive to neither UV nor gamma irradiation. Two genomic clones, rad26+ and cds1+, were found to suppress the hydroxyurea sensitivity of the aya14 mutant. Genetic analysis indicates that aya14 is a novel allele of the cell cycle checkpoint gene rad26+, which we have named rad26.a14. cds1+ is a suppressor which suppresses the S-phase feedback control defect of rad26.a14 when S phase is inhibited by either hydroxyurea or cdc22, but it does not suppress the defect when S phase is arrested by a mutant DNA polymerase. Analyses of rad26.a14 in a variety of cdc mutant backgrounds indicate that strains containing rad26.a14 bypass S-phase arrest but not G1 or late S/G2 arrest. A model of how Rad26 monitors S-phase progression to maintain the dependency of cell cycle events and coordinates with other rad/hus checkpoint gene products in responding to radiation damage is proposed.

摘要

为携带DNA聚合酶δ(pol δ ts03)热敏等位基因的粟酒裂殖酵母菌株定义了一种半许可生长条件。在这种条件下,DNA聚合酶δ功能半失活,导致S期进程延迟。我们采用遗传策略分离出一组突变体,这些突变体在DNA复制不完全时进入早熟有丝分裂,但在DNA损伤后G2/M期阻滞方面没有缺陷。我们对aya14突变体进行了表征,当通过遗传或化学手段使S期阻滞时,该突变体进入早熟有丝分裂。然而,该突变体对紫外线和γ射线均不敏感。发现两个基因组克隆rad26 +和cds1 +可抑制aya14突变体对羟基脲的敏感性。遗传分析表明aya14是细胞周期检查点基因rad26 +的一个新等位基因,并将其命名为rad26.a14。cds1 +是一种抑制因子,当S期被羟基脲或cdc22抑制时,它可抑制rad26.a14的S期反馈控制缺陷,但当S期被突变的DNA聚合酶阻滞时,它不能抑制该缺陷。在多种cdc突变背景下对rad26.a14进行分析表明,含有rad26.a14的菌株绕过S期阻滞,但不绕过G1期或S期后期/G2期阻滞。我们提出了一个关于Rad26如何监测S期进程以维持细胞周期事件依赖性,并与其他rad/hus检查点基因产物协同应对辐射损伤的模型。

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