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

被引:135
作者
Dantzer, F
Nasheuer, HP
Vonesch, JL
de Murcia, G
Menissier-De Murcia, J
机构
[1] Ecole Super Biotechnol Strasbourg, CEA 14, CNRS, UPR 9003, F-67400 Illkirch Graffenstaden, France
[2] Inst Molek Biotechnol, D-07745 Jena, Germany
[3] Coll France, CNRS, INSERM, ULP,Inst Genet & Biol Mol & Cellulaire, F-67404 Illkirch Graffenstaden, France
关键词
D O I
10.1093/nar/26.8.1891
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
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 PARR 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 PARR 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.
引用
收藏
页码:1891 / 1898
页数:8
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