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MCM8/9 复合物:参与基因组维护的解旋酶中的新成员。

The MCM8/9 complex: A recent recruit to the roster of helicases involved in genome maintenance.

机构信息

Department of Chemistry and Biochemistry, Baylor University, Waco, Texas, 76798, USA.

Department of Chemistry and Biochemistry, Baylor University, Waco, Texas, 76798, USA.

出版信息

DNA Repair (Amst). 2019 Apr;76:1-10. doi: 10.1016/j.dnarep.2019.02.003. Epub 2019 Feb 5.

Abstract

There are several DNA helicases involved in seemingly overlapping aspects of homologous and homoeologous recombination. Mutations of many of these helicases are directly implicated in genetic diseases including cancer, rapid aging, and infertility. MCM8/9 are recent additions to the catalog of helicases involved in recombination, and so far, the evidence is sparse, making assignment of function difficult. Mutations in MCM8/9 correlate principally with primary ovarian failure/insufficiency (POF/POI) and infertility indicating a meiotic defect. However, they also act when replication forks collapse/break shuttling products into mitotic recombination and several mutations are found in various somatic cancers. This review puts MCM8/9 in context with other replication and recombination helicases to narrow down its genomic maintenance role. We discuss the known structure/function relationship, the mutational spectrum, and dissect the available cellular and organismal data to better define its role in recombination.

摘要

有几种 DNA 解旋酶参与同源重组和同系重组的相似方面。这些解旋酶中的许多突变直接与包括癌症、快速衰老和不育在内的遗传疾病有关。MCM8/9 是参与重组的解旋酶目录中的最新成员,到目前为止,证据很少,因此很难确定其功能。MCM8/9 的突变主要与原发性卵巢功能衰竭/不足(POF/POI)和不育相关,表明减数分裂缺陷。然而,当复制叉崩溃/断裂时,它们也会发生,将产物穿梭到有丝分裂重组中,并且在各种体细胞癌中发现了几种突变。这篇综述将 MCM8/9 置于其他复制和重组解旋酶的背景下,以缩小其基因组维持作用。我们讨论了已知的结构/功能关系,突变谱,并剖析了现有的细胞和机体数据,以更好地定义其在重组中的作用。

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