Mediation of proliferating cell nuclear antigen (PCNA)-dependent DNA replication through a conserved p21Cip1-like PCNA-binding motif present in the third subunit of human DNA polymerase δ

被引:89
|
作者
Ducoux, M
Urbach, S
Baldacci, G
Hübscher, U
Koundrioukoff, S
Christensen, J
Hughes, P
机构
[1] Ctr Univ Orsay, CNRS, UMR 2027, Inst Curie, F-91405 Orsay, France
[2] Univ Zurich Irchel, Dept Vet Biochem, CH-8057 Zurich, Switzerland
[3] Univ Copenhagen, Dept Immunol & Microbiol, DK-2200 Copenhagen, Denmark
关键词
D O I
10.1074/jbc.M106990200
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
The subunit that mediates binding of proliferating cell nuclear antigen (PCNA) to human DNA polymerase delta has not been clearly defined. We show that the third subunit of human DNA polymerase delta, p66, interacts with PCNA through a canonical PCNA-binding sequence located in its C terminus. Conversely, p66 interacts with the domain-interconnecting loop of PCNA, a region previously shown to be important for DNA polymerase delta activity and for binding of the cell cycle inhibitor P21(CiP1). In accordance with this, a peptide containing the PCNA-binding domain of p21(CiP1) inhibited p66 binding to PCNA and the activity of native three-subunit DNA polymerase delta. Furthermore, pull-down assays showed that DNA polymerase delta requires p66 for interaction with PCNA. More importantly, only reconstituted three-subunit DNA polymerase delta displayed PCNA-dependent DNA replication that could be inhibited by the PCNA-binding domain of p21(CiP1). Direct participation of p66 in PCNA-dependent DNA replication in vivo is demonstrated by co-localization of p66 with PCNA and DNA polymerase 8 within DNA replication foci. Finally, in vitro phosphorylation of p66 by cyclin-dependent kinases suggests that p66 activity may be subject to cell cycle-dependent regulation. These results suggest that p66 is the chief mediator of PCNA-dependent DNA synthesis by DNA polymerase delta.
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收藏
页码:49258 / 49266
页数:9
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