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Cdc6和ORC依次进行ATP水解引导Mcm2-7解旋酶的装载。

Sequential ATP hydrolysis by Cdc6 and ORC directs loading of the Mcm2-7 helicase.

作者信息

Randell John C W, Bowers Jayson L, Rodríguez Heather K, Bell Stephen P

机构信息

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

出版信息

Mol Cell. 2006 Jan 6;21(1):29-39. doi: 10.1016/j.molcel.2005.11.023.

Abstract

Loading of the Mcm2-7 DNA replicative helicase onto origin-proximal DNA is a critical and tightly regulated event during the initiation of eukaryotic DNA replication. The resulting protein-DNA assembly is called the prereplicative complex (pre-RC), and its formation requires the origin recognition complex (ORC), Cdc6, Cdt1, and ATP. ATP hydrolysis by ORC is required for multiple rounds of Mcm2-7 loading. Here, we investigate the role of ATP hydrolysis by Cdc6 during pre-RC assembly. We find that Cdc6 is an ORC- and origin DNA-dependent ATPase that functions at a step preceding ATP hydrolysis by ORC. Inhibiting Cdc6 ATP hydrolysis stabilizes Cdt1 on origin DNA and prevents Mcm2-7 loading. In contrast, the initial association of Mcm2-7 with the other pre-RC components does not require ATP hydrolysis by Cdc6. Importantly, these coordinated yet distinct functions of ORC and Cdc6 ensure the correct temporal and spatial regulation of pre-RC formation.

摘要

将Mcm2-7 DNA复制解旋酶加载到靠近起始点的DNA上是真核生物DNA复制起始过程中的一个关键且受到严格调控的事件。由此产生的蛋白质-DNA组装体称为复制前复合体(pre-RC),其形成需要起始点识别复合体(ORC)、Cdc6、Cdt1和ATP。ORC进行ATP水解是多轮加载Mcm2-7所必需的。在这里,我们研究了Cdc6在pre-RC组装过程中ATP水解的作用。我们发现Cdc6是一种依赖于ORC和起始点DNA的ATP酶,其作用于ORC进行ATP水解之前的步骤。抑制Cdc6的ATP水解可使Cdt1稳定在起始点DNA上,并阻止Mcm2-7的加载。相反,Mcm2-7与其他pre-RC组分的初始结合并不需要Cdc6进行ATP水解。重要的是,ORC和Cdc6的这些协调但不同的功能确保了pre-RC形成的正确时空调控。

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