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复制前复合体组装过程中的瞬时双链DNA断裂。

Transient dsDNA breaks during pre-replication complex assembly.

作者信息

Rampakakis Emmanouil, Zannis-Hadjopoulos Maria

机构信息

Goodman Cancer Center and Department of Biochemistry, McGill University, Montreal, Quebec, Canada H3A 1A3.

出版信息

Nucleic Acids Res. 2009 Sep;37(17):5714-24. doi: 10.1093/nar/gkp617. Epub 2009 Jul 28.

Abstract

Initiation of DNA replication involves the ordered assembly of the multi-protein pre-replicative complex (pre-RC) during G(1) phase. Previously, DNA topoisomerase II (topo II) was shown to associate with the DNA replication origin located in the lamin B2 gene locus in a cell-cycle-modulated manner. Here we report that activation of both the early-firing lamin B2 and the late-firing hOrs8 human replication origins involves DNA topo II-dependent, transient, site-specific dsDNA-break formation. Topo IIbeta in complex with the DNA repair protein Ku associates in vivo and in vitro with the pre-RC region, introducing dsDNA breaks in a biphasic manner, during early and mid-G(1) phase. Inhibition of topo II activity interferes with the pre-RC assembly resulting in prolonged G(1) phase. The data mechanistically link DNA topo IIbeta-dependent dsDNA breaks and the components of the DNA repair machinery with the initiation of DNA replication and suggest an important role for DNA topology in origin activation.

摘要

DNA复制的起始涉及多蛋白前复制复合体(pre-RC)在G1期的有序组装。此前研究表明,DNA拓扑异构酶II(topo II)以细胞周期调控的方式与位于层粘连蛋白B2基因位点的DNA复制起点相关联。在此我们报告,早期激活的层粘连蛋白B2和晚期激活的hOrs8人类复制起点的激活均涉及DNA topo II依赖性、瞬时、位点特异性双链DNA断裂的形成。与DNA修复蛋白Ku形成复合体的Topo IIβ在体内和体外均与pre-RC区域相关联,在G1期早期和中期以双相方式引入双链DNA断裂。抑制topo II活性会干扰pre-RC组装,导致G1期延长。这些数据从机制上把DNA topo IIβ依赖性双链DNA断裂以及DNA修复机制的组分与DNA复制的起始联系起来,并提示DNA拓扑结构在起点激活中具有重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d3b/2761281/402dec876558/gkp617f1.jpg

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