Gaillard Pierre-Henri L, Noguchi Eishi, Shanahan Paul, Russell Paul
Department of Molecular Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, CA 92037, USA.
Mol Cell. 2003 Sep;12(3):747-59. doi: 10.1016/s1097-2765(03)00342-3.
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.
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。