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减数分裂重组:两种重组酶的协同作用

Meiotic recombination: an affair of two recombinases.

作者信息

Sehorn Michael G, Sung Patrick

机构信息

Department of Molecular Biophysics and Biochemistry, Yale University School of Medicine, New Haven, Connecticut 06520-8024, USA.

出版信息

Cell Cycle. 2004 Nov;3(11):1375-7. doi: 10.4161/cc.3.11.1364. Epub 2004 Nov 20.

Abstract

In E. coli, homologous recombination is catalyzed by the RecA recombinase. Two RecA-like factors, Rad51 and Dmc1, are found in eukaryotes. Whereas Rad51 is needed for homologous recombination reactions in both mitotic and meiotic cells, the role of Dmc1 is restricted to meiosis. Recent work has shown that, like RecA and Rad51, Dmc1 mediates the homologous DNA pairing strand exchange reaction via a filamentous intermediate assembled on single-stranded DNA. Emerging evidence suggests that the tumor suppressor BRCA2 functions in the assembly of nucleoprotein filaments of Rad51 and Dmc1. The manner in which Rad51 and Dmc1 functionally cooperate in meiotic recombination remains to be determined.

摘要

在大肠杆菌中,同源重组由RecA重组酶催化。真核生物中发现了两种类RecA因子,即Rad51和Dmc1。Rad51在有丝分裂和减数分裂细胞的同源重组反应中都是必需的,而Dmc1的作用仅限于减数分裂。最近的研究表明,与RecA和Rad51一样,Dmc1通过在单链DNA上组装的丝状中间体介导同源DNA配对链交换反应。新出现的证据表明,肿瘤抑制因子BRCA2在Rad51和Dmc1的核蛋白丝组装中发挥作用。Rad51和Dmc1在减数分裂重组中功能协作的方式仍有待确定。

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