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由哺乳动物细胞活性催化的分支迁移和霍利迪连接点解析。

Branch migration and Holliday junction resolution catalyzed by activities from mammalian cells.

作者信息

Constantinou A, Davies A A, West S C

机构信息

Imperial Cancer Research Fund, Clare Hall Laboratories, Blanche Lane, South Mimms, EN6 3LD, Hertfordshire, United Kingdom.

出版信息

Cell. 2001 Jan 26;104(2):259-68. doi: 10.1016/s0092-8674(01)00210-0.

Abstract

During homologous recombination, DNA strand exchange leads to Holliday junction formation. The movement, or branch migration, of this junction along DNA extends the length of the heteroduplex joint. In prokaryotes, branch migration and Holliday junction resolution are catalyzed by the RuvA and RuvB proteins, which form a complex with RuvC resolvase to form a "resolvasome". Mammalian cell-free extracts have now been fractionated to reveal analogous activities. An ATP-dependent branch migration activity, which migrates junctions through >2700 bp, cofractionates with the Holliday junction resolvase during several chromatographic steps. Together, the two activities promote concerted branch migration/resolution reactions similar to those catalyzed by E. coli RuvABC, highlighting the preservation of this essential pathway in recombination and DNA repair from prokaryotes to mammals.

摘要

在同源重组过程中,DNA链交换导致霍利迪连接体的形成。该连接体沿DNA的移动,即分支迁移,会延长异源双链接头的长度。在原核生物中,分支迁移和霍利迪连接体的解离由RuvA和RuvB蛋白催化,它们与RuvC解离酶形成复合物以形成“解离体”。现在已经对哺乳动物无细胞提取物进行了分级分离以揭示类似的活性。一种依赖ATP的分支迁移活性,可使连接体迁移超过2700 bp,在几个色谱步骤中与霍利迪连接体解离酶共分级。这两种活性共同促进了类似于大肠杆菌RuvABC催化的协同分支迁移/解离反应,突出了从原核生物到哺乳动物在重组和DNA修复中这一基本途径的保守性。

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