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真核细胞核DNA聚合酶的复制编排:与辅助蛋白的特异性相互作用将DNA聚合酶α、δ和ε排列在复制体中,用于前导链和后随链DNA复制。

Arranging eukaryotic nuclear DNA polymerases for replication: Specific interactions with accessory proteins arrange Pols α, δ, and ϵ in the replisome for leading-strand and lagging-strand DNA replication.

作者信息

Kunkel Thomas A, Burgers Peter M J

机构信息

Genome Integrity and Structural Biology Laboratory, National Institute of Environmental Health Sciences, NIH, DHHS, Research Triangle Park, NC, USA.

Department of Biochemistry and Molecular Biophysics, Washington University School of Medicine, St. Louis, MO, USA.

出版信息

Bioessays. 2017 Aug;39(8). doi: 10.1002/bies.201700070.

Abstract

Biochemical and cryo-electron microscopy studies have just been published revealing interactions among proteins of the yeast replisome that are important for highly coordinated synthesis of the two DNA strands of the nuclear genome. These studies reveal key interactions important for arranging DNA polymerases α, δ, and ϵ for leading and lagging strand replication. The CMG (Mcm2-7, Cdc45, GINS) helicase is central to this interaction network. These are but the latest examples of elegant studies performed in the recent past that lead to a much better understanding of how the eukaryotic replication fork achieves efficient DNA replication that is accurate enough to prevent diseases yet allows evolution.

摘要

生化和冷冻电子显微镜研究刚刚发表,揭示了酵母复制体中蛋白质之间的相互作用,这些相互作用对于核基因组两条DNA链的高度协调合成至关重要。这些研究揭示了对于排列DNA聚合酶α、δ和ε以进行前导链和后随链复制很重要的关键相互作用。CMG(Mcm2-7、Cdc45、GINS)解旋酶是这个相互作用网络的核心。这些只是近期进行的出色研究的最新例子,这些研究使人们对真核生物复制叉如何实现高效DNA复制有了更好的理解,这种复制足够精确以预防疾病,同时又允许进化。

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Mechanism of Lagging-Strand DNA Replication in Eukaryotes.真核生物滞后链 DNA 复制的机制。
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Eukaryotic DNA Replication Fork.真核生物DNA复制叉
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