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本文引用的文献

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The distribution of the numbers of mutants in bacterial populations.细菌群体中突变体数量的分布。
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2
Minor groove interactions at the DNA polymerase beta active site modulate single-base deletion error rates.DNA聚合酶β活性位点的小沟相互作用调节单碱基缺失错误率。
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3
Saccharomyces cerevisiae pol30 (proliferating cell nuclear antigen) mutations impair replication fidelity and mismatch repair.酿酒酵母pol30(增殖细胞核抗原)突变会损害复制保真度和错配修复。
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Novel DNA polymerases offer clues to the molecular basis of mutagenesis.新型DNA聚合酶为诱变的分子基础提供了线索。
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Direct interaction of proliferating cell nuclear antigen with the p125 catalytic subunit of mammalian DNA polymerase delta.增殖细胞核抗原与哺乳动物DNA聚合酶δ的p125催化亚基的直接相互作用。
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Gross chromosomal rearrangements in Saccharomyces cerevisiae replication and recombination defective mutants.酿酒酵母复制和重组缺陷突变体中的染色体大片段重排
Nat Genet. 1999 Sep;23(1):81-5. doi: 10.1038/12687.
7
Protein kinase activity and identification of a toxic effector domain of the target of rapamycin TOR proteins in yeast.酵母中雷帕霉素靶蛋白TOR的蛋白激酶活性及毒性效应结构域的鉴定
Mol Biol Cell. 1999 Aug;10(8):2531-46. doi: 10.1091/mbc.10.8.2531.
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Multiple pathways of recombination induced by double-strand breaks in Saccharomyces cerevisiae.酿酒酵母中双链断裂诱导的多种重组途径。
Microbiol Mol Biol Rev. 1999 Jun;63(2):349-404. doi: 10.1128/MMBR.63.2.349-404.1999.
9
Detection of mutations in the DNA polymerase delta gene of human sporadic colorectal cancers and colon cancer cell lines.人类散发性结直肠癌及结肠癌细胞系中DNA聚合酶δ基因的突变检测
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10
A mutation of the yeast gene encoding PCNA destabilizes both microsatellite and minisatellite DNA sequences.编码增殖细胞核抗原的酵母基因突变会使微卫星和小卫星DNA序列不稳定。
Genetics. 1999 Feb;151(2):511-9. doi: 10.1093/genetics/151.2.511.

由编码DNA聚合酶δ的酵母基因突变或DNA聚合酶δ细胞水平降低所产生的基因组缺失率增加。

Increased rates of genomic deletions generated by mutations in the yeast gene encoding DNA polymerase delta or by decreases in the cellular levels of DNA polymerase delta.

作者信息

Kokoska R J, Stefanovic L, DeMai J, Petes T D

机构信息

Department of Biology, Curriculum in Genetics and Molecular Biology, University of North Carolina, Chapel Hill, North Carolina 27599-3280, USA.

出版信息

Mol Cell Biol. 2000 Oct;20(20):7490-504. doi: 10.1128/MCB.20.20.7490-7504.2000.

DOI:10.1128/MCB.20.20.7490-7504.2000
PMID:11003646
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC86302/
Abstract

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.

摘要

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。