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对真核生物DNA复制起始的见解

Insights into the Initiation of Eukaryotic DNA Replication.

作者信息

Bruck Irina, Perez-Arnaiz Patricia, Colbert Max K, Kaplan Daniel L

机构信息

a Department of Biomedical Science; Florida State University College of Medicine ; Tallahassee , FL USA.

出版信息

Nucleus. 2015;6(6):449-54. doi: 10.1080/19491034.2015.1115938. Epub 2015 Dec 28.

Abstract

The initiation of DNA replication is a highly regulated event in eukaryotic cells to ensure that the entire genome is copied once and only once during S phase. The primary target of cellular regulation of eukaryotic DNA replication initiation is the assembly and activation of the replication fork helicase, the 11-subunit assembly that unwinds DNA at a replication fork. The replication fork helicase, called CMG for Cdc45-Mcm2-7, and GINS, assembles in S phase from the constituent Cdc45, Mcm2-7, and GINS proteins. The assembly and activation of the CMG replication fork helicase during S phase is governed by 2 S-phase specific kinases, CDK and DDK. CDK stimulates the interaction between Sld2, Sld3, and Dpb11, 3 initiation factors that are each required for the initiation of DNA replication. DDK, on the other hand, phosphorylates the Mcm2, Mcm4, and Mcm6 subunits of the Mcm2-7 complex. Sld3 recruits Cdc45 to Mcm2-7 in a manner that depends on DDK, and recent work suggests that Sld3 binds directly to Mcm2-7 and also to single-stranded DNA. Furthermore, recent work demonstrates that Sld3 and its human homolog Treslin substantially stimulate DDK phosphorylation of Mcm2. These data suggest that the initiation factor Sld3/Treslin coordinates the assembly and activation of the eukaryotic replication fork helicase by recruiting Cdc45 to Mcm2-7, stimulating DDK phosphorylation of Mcm2, and binding directly to single-stranded DNA as the origin is melted.

摘要

在真核细胞中,DNA复制的起始是一个受到高度调控的事件,以确保整个基因组在S期被复制一次且仅复制一次。真核生物DNA复制起始的细胞调控的主要靶点是复制叉解旋酶的组装和激活,复制叉解旋酶是一种由11个亚基组成的复合物,它在复制叉处解开DNA双链。复制叉解旋酶,即由Cdc45、Mcm2-7和GINS组成的CMG复合物,在S期由其组成蛋白Cdc45、Mcm2-7和GINS组装而成。CMG复制叉解旋酶在S期的组装和激活由两种S期特异性激酶CDK和DDK控制。CDK刺激Sld2、Sld3和Dpb11之间的相互作用,这三种起始因子都是DNA复制起始所必需的。另一方面,DDK使Mcm2-7复合物的Mcm2、Mcm4和Mcm6亚基磷酸化。Sld3以依赖于DDK的方式将Cdc45招募到Mcm2-7上,最近的研究表明Sld3直接与Mcm2-7以及单链DNA结合。此外,最近的研究表明Sld3及其人类同源物Treslin能显著刺激Mcm2的DDK磷酸化。这些数据表明,起始因子Sld3/Treslin通过将Cdc45招募到Mcm2-7、刺激Mcm2的DDK磷酸化以及在复制起点解链时直接与单链DNA结合,来协调真核生物复制叉解旋酶的组装和激活。

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Insights into the Initiation of Eukaryotic DNA Replication.对真核生物DNA复制起始的见解
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