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Functional association of poly(ADP-ribose) polymerase with DNA polymerase alpha-primase complex: a link between DNA strand break detection and DNA replication.

机译:聚(ADP-核糖)聚合酶与DNA聚合酶α-primase复杂的功能关联:DNA链断裂检测和DNA复制之间的联系。

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摘要

Poly(ADP-ribose) polymerase (PARP) is an element of the DNA damage surveillance network evolved by eukaryotic cells to cope with numerous environmental and endogenous genotoxic agents. PARP has been found to be involved in vivo in both cell proliferation and base excision repair of DNA. In this study the interaction between PARP and the DNA polymerase alpha-primase tetramer has been examined. We provide evidence that in proliferating cells: (i) PARP is physically associated with the catalytic subunit of the DNA polymerase alpha-primase tetramer, an association confirmed by confocal microscopy, demonstrating that both enzymes are co-localized at the nuclear periphery of HeLa cells; (ii) this interaction requires the integrity of the second zinc finger of PARP and is maximal during the S and G2/M phases of the cell cycle; (iii) PARP-deficient cells derived from PARP knock-out mice exhibited reduced DNA polymerase activity, compared with the parental cells, a reduction accentuated following exposure to sublethal doses of methylmethanesulfonate. Altogether, the present results strongly suggest that PARP participates in a DNA damage survey mechanism implying its nick-sensor function as part of the control of replication fork progression when breaks are present in the template.
机译:聚(ADP-核糖)聚合酶(PARP)是由真核细胞进化以应对众多环境和内源性遗传毒性试剂的DNA损伤监测网络的组成部分。已经发现PARP在体内参与DNA的细胞增殖和碱基切除修复。在这项研究中,已经研究了PARP和DNA聚合酶α-primase四聚体之间的相互作用。我们提供的证据表明,在增殖的细胞中:(i)PARP与DNA聚合酶α-primase四聚体的催化亚基物理相关,这是通过共聚焦显微镜证实的,表明这两种酶共定位于HeLa细胞的核周边; (ii)这种相互作用需要PARP的第二个锌指的完整性,并且在细胞周期的S和G2 / M阶段最大。 (iii)与亲代细胞相比,源自PARP基因敲除小鼠的PARP缺陷细胞表现出降低的DNA聚合酶活性,这种降低在暴露于亚致死剂量的甲基磺酸甲酯后加剧。总体而言,本结果强烈表明,当模板中存在断裂时,PARP参与DNA损伤调查机制,这暗示其缺口传感器功能是控制复制叉进程的一部分。

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