Kumagai, Akiko and Kim, Soo-Mi and Dunphy, William G. (2004) Claspin and the Activated Form of ATR-ATRIP Collaborate in the Activation of Chk1. Journal of Biological Chemistry, 279 (48). pp. 49599-49608. ISSN 0021-9258. http://resolver.caltech.edu/CaltechAUTHORS:KUMjbc04
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Claspin is necessary for the ATR-dependent activation of Chk1 in Xenopus egg extracts containing incompletely replicated DNA. ATR possesses a regulatory partner called ATRIP. We have studied the respective roles of ATR-ATRIP and Claspin in the activation of Chk1. ATR-ATRIP bound well to various DNA templates in Xenopus egg extracts. ATR-ATRIP bound to a single-stranded DNA template was weakly active. By contrast, the ATR-ATRIP complex on a DNA template containing both single- and double-stranded regions displayed a large increase in kinase activity. This observation suggests that ATR-ATRIP normally undergoes activation upon association with specific nucleic acid structures at DNA replication forks. Without Claspin, activated ATR-ATRIP phosphorylated Chk1 weakly in a cell-free reaction. The addition of Claspin to this reaction strongly stimulated the phosphorylation of Chk1 by ATR-ATRIP. Claspin also induced significant autophosphorylation of Chk1 in the absence of ATR-ATRIP. Taken together, these results indicate that the checkpoint-dependent phosphorylation of Chk1 is a multistep process involving activation of the ATR-ATRIP complex at replication forks and presentation of Chk1 to this complex by Claspin.
|Additional Information:||© 2004 the American Society for Biochemistry and Molecular Biology. Received for publication, July 23, 2004, and in revised form, September 13, 2004. We are grateful to our colleagues in the laboratory for helpful comments on the manuscript. This work was supported in part by National Institutes of Health Grants GM043974 and GM070891. The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact. The nucleotide sequence(s) reported in this paper has been submitted to the GenBankTM/EBI Data Bank with accession number(s) AY644453.|
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|Deposited On:||04 Dec 2006|
|Last Modified:||04 Nov 2016 17:43|
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