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内源性Mus81-Eme1复合物通过切口和反切口机制解析霍利迪连接体。

The endogenous Mus81-Eme1 complex resolves Holliday junctions by a nick and counternick mechanism.

作者信息

Gaillard Pierre-Henri L, Noguchi Eishi, Shanahan Paul, Russell Paul

机构信息

Department of Molecular Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.

出版信息

Mol Cell. 2003 Sep;12(3):747-59. doi: 10.1016/s1097-2765(03)00342-3.

Abstract

Functional studies strongly suggest that the Mus81-Eme1 complex resolves Holliday junctions (HJs) in fission yeast, but in vitro it preferentially cleaves flexible three-way branched structures that model replication forks or 3' flaps. Here we report that a nicked HJ is the preferred substrate of endogenous and recombinant Mus81-Eme1. Cleavage occurs specifically on the strand that opposes the nick, resulting in resolution of the structure into linear duplex products. Resolving cuts made by the endogenous Mus81-Eme1 complex on an intact HJ are quasi-simultaneous, indicating that Mus81-Eme1 resolves HJs by a nick and counternick mechanism, with a large rate enhancement of the second cut arising from the flexible nature of the nicked HJ intermediate. Recombinant Mus81-Eme1 is ineffective at making the first cut. We also report that HJs accumulate in a DNA polymerase alpha mutant that lacks Mus81, providing further evidence that the Mus81-Eme1 complex targets HJs in vivo.

摘要

功能研究有力地表明,在裂殖酵母中,Mus81-Eme1复合物可拆分霍利迪连接体(HJs),但在体外,它优先切割模拟复制叉或3' 瓣的柔性三链分支结构。在此,我们报告带切口的HJ是内源性和重组Mus81-Eme1的首选底物。切割特异性地发生在与切口相对的链上,导致该结构分解为线性双链产物。内源性Mus81-Eme1复合物在完整HJ上进行的拆分切割几乎是同时发生的,这表明Mus81-Eme1通过切口和反切口机制拆分HJs,由于带切口的HJ中间体的柔性,第二次切割的速率大幅提高。重组Mus81-Eme1在进行第一次切割时效率低下。我们还报告说,在缺乏Mus81的DNA聚合酶α突变体中,HJs会积累,这进一步证明Mus81-Eme1复合物在体内靶向HJs。

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