Linking PCNA-dependent replication and ATR by human claspin

被引:11
作者
Brondello, Jean-Marc [1 ]
Ducommun, Bernard
Fernandez, Anne
Lamb, Ned J.
机构
[1] CRLC Val dAurelle, INSERM, EMI 0229, F-34298 Montpellier 5, France
[2] Univ Toulouse 3, LBCMCP, CNRS, UMR5088,IFR 109, F-31062 Toulouse, France
[3] CNRS, UPR 1142, Cell Biol Unit, Inst Genet Humaine, F-34396 Montpellier 5, France
关键词
DNA; damage checkpoint; ATR; claspin; PCNA; replication;
D O I
10.1016/j.bbrc.2007.01.091
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
Recent studies in Xenopus have identified a new checkpoint protein called Claspin that is believed to transduce the checkpoint DNA damage signals to Chk1 kinase. Here we show that the human Claspin homolog is a chromatin bound protein either in the absence or in the presence of damaged DNA, independent of its association with ATR. Furthermore, we show that human Claspin is found in complex with PCNA, an essential component of the DNA replication machinery, and is released upon DNA replication arrest. Interfering with PCNA function by overexpression of p21 mutant, impaired in its interaction with Cdks but not with PCNA, leads to ATR-dependent Chk1 activation. These findings suggest that the dissociation of Claspin-PCNA could be part of the signal leading to Chk1 activation. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:1028 / 1033
页数:6
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