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如何将复制性解旋酶加载到染色质上:在进化过程中这一问题愈发复杂。

How to load a replicative helicase onto chromatin: a more and more complex matter during evolution.

作者信息

Lutzmann Malik, Méchali Marcel

机构信息

Institute of Human Genetics, CNRS, Montpellier, France.

出版信息

Cell Cycle. 2009 May 1;8(9):1309-13. doi: 10.4161/cc.8.9.8216. Epub 2009 May 18.

Abstract

In all eukaryotes, the heterohexameric MCM2-7 complex functions as the main replicative helicase during S phase. During early G1 phase, it is recruited onto chromatin in a sequence of reactions called pre-replication complex (pre-RC) formation or DNA licensing. This process is ATP-dependent and at least two different chromatin-bound ATPase activities are required besides several others essential, but not enzymatically active, proteins. Although functionally conserved during evolution, pre-RC formation and the way the MCM2-7 helicase is loaded onto DNA are more complex in metazoans than in single-cell eukaryotes. Recently, we characterized a new essential factor for pre-RC assembly and DNA licensing, the vertebrate-specific MCM9 protein that contains not only an ATPase but also a helicase domain. MCM9 adds another layer of complexity to how vertebrates achieve and regulate the loading of the MCM2-7 helicase and DNA replication.

摘要

在所有真核生物中,异源六聚体MCM2 - 7复合物在S期作为主要的复制解旋酶发挥作用。在G1期早期,它通过一系列称为复制前复合物(pre - RC)形成或DNA许可的反应被招募到染色质上。这个过程是ATP依赖的,除了其他几种必需但无酶活性的蛋白质外,还需要至少两种不同的与染色质结合的ATP酶活性。尽管在进化过程中功能保守,但后生动物中pre - RC的形成以及MCM2 - 7解旋酶加载到DNA上的方式比单细胞真核生物更为复杂。最近,我们鉴定了一种pre - RC组装和DNA许可的新的必需因子,即脊椎动物特异性的MCM9蛋白,它不仅含有一个ATP酶结构域,还含有一个解旋酶结构域。MCM9为脊椎动物实现和调节MCM2 - 7解旋酶的加载及DNA复制增加了另一层复杂性。

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