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前复制复合物组装的动力学。

Dynamics of pre-replicative complex assembly.

机构信息

Department of Biology, Cambridge, Massachusetts 02139.

Department of Biology, Cambridge, Massachusetts 02139; Howard Hughes Medical Institute, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139.

出版信息

J Biol Chem. 2010 Mar 26;285(13):9437-9443. doi: 10.1074/jbc.M109.072504. Epub 2010 Jan 22.

Abstract

The pre-replicative complex (pre-RC) is formed at all potential origins of replication through the action of the origin recognition complex (ORC), Cdc6, Cdt1, and the Mcm2-7 complex. The end result of pre-RC formation is the loading of the Mcm2-7 replicative helicase onto origin DNA. We examined pre-RC formation in vitro and found that it proceeds through separable binding events. Origin-bound ORC recruits Cdc6, and this ternary complex then promotes helicase loading in the presence of a pre-formed Mcm2-7-Cdt1 complex. Using a stepwise pre-RC assembly assay, we investigated the fate of pre-RC components during later stages of the reaction. We determined that helicase loading is accompanied by dissociation of ORC, Cdc6, and Cdt1 from origin DNA. This dissociation requires ATP hydrolysis at a late stage of pre-RC assembly. Our results indicate that pre-RC formation is a dynamic process.

摘要

前复制复合物(pre-RC)通过原点识别复合物(ORC)、Cdc6、Cdt1 和 Mcm2-7 复合物的作用在所有潜在的复制起点形成。 pre-RC 形成的最终结果是将 Mcm2-7 复制解旋酶加载到原点 DNA 上。我们在体外检查了 pre-RC 的形成,发现它通过可分离的结合事件进行。原点结合的 ORC 招募 Cdc6,然后在预形成的 Mcm2-7-Cdt1 复合物存在的情况下促进解旋酶加载。使用逐步的 pre-RC 组装测定法,我们研究了反应后期 pre-RC 成分的命运。我们确定解旋酶加载伴随着 ORC、Cdc6 和 Cdt1 从原点 DNA 解离。这种解离需要在 pre-RC 组装的后期阶段进行 ATP 水解。我们的结果表明,pre-RC 的形成是一个动态过程。

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本文引用的文献

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