Kokoska R J, Stefanovic L, DeMai J, Petes T D
Department of Biology, Curriculum in Genetics and Molecular Biology, University of North Carolina, Chapel Hill, North Carolina 27599-3280, USA.
Mol Cell Biol. 2000 Oct;20(20):7490-504. doi: 10.1128/MCB.20.20.7490-7504.2000.
In Saccharomyces cerevisiae, POL3 encodes the catalytic subunit of DNA polymerase delta. While yeast POL3 mutant strains that lack the proofreading exonuclease activity of the polymerase have a strong mutator phenotype, little is known regarding the role of other Pol3p domains in mutation avoidance. We identified a number of pol3 mutations in regions outside of the exonuclease domain that have a mutator phenotype, substantially elevating the frequency of deletions. These deletions appear to reflect an increased frequency of DNA polymerase slippage. In addition, we demonstrate that reduction in the level of wild-type DNA polymerase results in a similar mutator phenotype. Lowered levels of DNA polymerase also result in increased sensitivity to the DNA-damaging agent methyl methane sulfonate. We conclude that both the quantity and the quality of DNA polymerase delta is important in ensuring genome stability.
在酿酒酵母中,POL3编码DNA聚合酶δ的催化亚基。虽然缺乏聚合酶校对核酸外切酶活性的酵母POL3突变菌株具有强烈的突变体表型,但关于Pol3p其他结构域在避免突变中的作用知之甚少。我们在核酸外切酶结构域之外的区域鉴定出许多具有突变体表型的pol3突变,这些突变显著提高了缺失频率。这些缺失似乎反映了DNA聚合酶滑动频率的增加。此外,我们证明野生型DNA聚合酶水平的降低会导致类似的突变体表型。DNA聚合酶水平的降低还会导致对DNA损伤剂甲磺酸甲酯的敏感性增加。我们得出结论,DNA聚合酶δ的数量和质量对于确保基因组稳定性都很重要。