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真核生物DNA复制叉处的聚合酶动力学

Polymerase dynamics at the eukaryotic DNA replication fork.

作者信息

Burgers Peter M J

机构信息

Department of Biochemistry and Molecular Biophysics, Washington University School of Medicine, St. Louis, Missouri 63110, USA.

出版信息

J Biol Chem. 2009 Feb 13;284(7):4041-5. doi: 10.1074/jbc.R800062200. Epub 2008 Oct 3.

Abstract

This review discusses recent insights in the roles of DNA polymerases (Pol) delta and epsilon in eukaryotic DNA replication. A growing body of evidence specifies Pol epsilon as the leading strand DNA polymerase and Pol delta as the lagging strand polymerase during undisturbed DNA replication. New evidence supporting this model comes from the use of polymerase mutants that show an asymmetric mutator phenotype for certain mispairs, allowing an unambiguous strand assignment for these enzymes. On the lagging strand, Pol delta corrects errors made by Pol alpha during Okazaki fragment initiation. During Okazaki fragment maturation, the extent of strand displacement synthesis by Pol delta determines whether maturation proceeds by the short or long flap processing pathway. In the more common short flap pathway, Pol delta coordinates with the flap endonuclease FEN1 to degrade initiator RNA, whereas in the long flap pathway, RNA removal is initiated by the Dna2 nuclease/helicase.

摘要

本综述讨论了DNA聚合酶(Pol)δ和ε在真核生物DNA复制中作用的最新见解。越来越多的证据表明,在未受干扰的DNA复制过程中,Pol ε是前导链DNA聚合酶,而Pol δ是后随链聚合酶。支持该模型的新证据来自对聚合酶突变体的研究,这些突变体对某些错配显示出不对称的突变表型,从而能够明确确定这些酶所负责的链。在后随链上,Pol δ校正Pol α在冈崎片段起始过程中产生的错误。在冈崎片段成熟过程中,Pol δ进行链置换合成的程度决定了成熟过程是通过短瓣处理途径还是长瓣处理途径进行。在更常见的短瓣途径中,Pol δ与瓣内切酶FEN1协同作用以降解引发RNA,而在长瓣途径中,RNA的去除由Dna2核酸酶/解旋酶启动。

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Polymerase dynamics at the eukaryotic DNA replication fork.真核生物DNA复制叉处的聚合酶动力学
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