Song J M, Montelone B A, Siede W, Friedberg E C
Department of Pathology, Stanford University School of Medicine, California 94305.
J Bacteriol. 1990 Dec;172(12):6620-30. doi: 10.1128/jb.172.12.6620-6630.1990.
A yeast strain was constructed that had a disruption of the chromosomal RAD3 gene and carried a series of centromeric plasmids with defined mutations in this gene. Using this isogenic collection, we examined sensitivity to UV radiation, spontaneous and UV radiation-induced mutagenesis, and mitotic recombination. Several alleles resulted in a marked increase in UV sensitivity. Most of these alleles were found to carry mutations located in consensus motifs for DNA helicases. Other alleles caused a modest or no increase in UV sensitivity and carried mutations in regions of the Rad3 polypeptide that are apparently not conserved. This correlation suggests that the DNA helicase activity of Rad3 protein is required for nucleotide excision repair of DNA. Some rad3 alleles conferred a marked increase in the frequency of spontaneous mutagenesis, including nonsuppressor reversion of the lys2-1 ochre mutation. These alleles also showed a good correlation with conserved DNA helicase domains, suggesting that the Rad3 DNA helicase also plays a role in the fidelity of DNA synthesis or postreplicative mismatch correction. Several rad3 mutator alleles also resulted in increased levels of mitotic recombination. Increased spontaneous mutagenesis and mitotic recombination are characteristic features of the Rem- phenotype. However, in contrast to the prototypic Rem- phenotype, the rad3 mutator alleles identified in this study did not confer inviability in the presence of mutations in the RAD50 or RAD52 gene required for strand break repair of DNA.
构建了一种酵母菌株,其染色体RAD3基因被破坏,并携带一系列在该基因中具有特定突变的着丝粒质粒。利用这个同基因菌株库,我们检测了对紫外线辐射的敏感性、自发及紫外线辐射诱导的诱变以及有丝分裂重组。有几个等位基因导致对紫外线的敏感性显著增加。发现这些等位基因中的大多数携带位于DNA解旋酶共有基序中的突变。其他等位基因导致对紫外线的敏感性适度增加或没有增加,并且在Rad3多肽中明显不保守的区域携带突变。这种相关性表明,Rad3蛋白的DNA解旋酶活性是DNA核苷酸切除修复所必需的。一些rad3等位基因使自发诱变频率显著增加,包括lys2-1赭石突变的非抑制性回复突变。这些等位基因也与保守的DNA解旋酶结构域有良好的相关性,表明Rad3 DNA解旋酶在DNA合成保真度或复制后错配修复中也起作用。几个rad3诱变等位基因还导致有丝分裂重组水平增加。自发诱变和有丝分裂重组增加是Rem-表型的特征。然而,与典型的Rem-表型不同,本研究中鉴定的rad3诱变等位基因在DNA链断裂修复所需的RAD50或RAD52基因存在突变的情况下并不导致 inviability。