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DNA聚合酶ε及其在基因组稳定性中的作用。

DNA polymerase ε and its roles in genome stability.

作者信息

Henninger Erin E, Pursell Zachary F

机构信息

Department of Biochemistry and Molecular Biology, Tulane University School of Medicine, New Orleans, LA, USA.

出版信息

IUBMB Life. 2014 May;66(5):339-51. doi: 10.1002/iub.1276. Epub 2014 May 24.

Abstract

DNA Polymerase Epsilon (Pol ε) is one of three DNA Polymerases (along with Pol δ and Pol α) required for nuclear DNA replication in eukaryotes. Pol ε is comprised of four subunits, the largest of which is encoded by the POLE gene and contains the catalytic polymerase and exonuclease activities. The 3'-5' exonuclease proofreading activity is able to correct DNA synthesis errors and helps protect against genome instability. Recent cancer genome sequencing efforts have shown that 3% of colorectal and 7% of endometrial cancers contain mutations within the exonuclease domain of POLE and are associated with significantly elevated levels of single nucleotide substitutions (15-500 per Mb) and microsatellite stability. POLE mutations have also been found in other tumor types, though at lower frequency, suggesting roles in tumorigenesis more broadly in different tissue types. In addition to its proofreading activity, Pol ε contributes to genome stability through multiple mechanisms that are discussed in this review.

摘要

DNA聚合酶ε(Pol ε)是真核生物细胞核DNA复制所需的三种DNA聚合酶之一(另外两种是Pol δ和Pol α)。Pol ε由四个亚基组成,其中最大的亚基由POLE基因编码,包含催化性聚合酶和核酸外切酶活性。3'-5'核酸外切酶校对活性能够校正DNA合成错误,并有助于防止基因组不稳定。最近的癌症基因组测序研究表明,3%的结直肠癌和7%的子宫内膜癌在POLE核酸外切酶结构域内存在突变,并且与单核苷酸替换水平显著升高(每兆碱基15 - 500个)和微卫星稳定性相关。在其他肿瘤类型中也发现了POLE突变,尽管频率较低,这表明其在更广泛的不同组织类型肿瘤发生中发挥作用。除了校对活性外,Pol ε还通过多种机制促进基因组稳定性,本文将对此进行讨论。

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