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XB-ART-6598
J Cell Biol September 2, 2002; 158 (5): 863-72.

DNA replication is required for the checkpoint response to damaged DNA in Xenopus egg extracts.

Stokes MP , Van Hatten R , Lindsay HD , Michael WM .


Abstract
Alkylating agents, such as methyl methanesulfonate (MMS), damage DNA and activate the DNA damage checkpoint. Although many of the checkpoint proteins that transduce damage signals have been identified and characterized, the mechanism that senses the damage and activates the checkpoint is not yet understood. To address this issue for alkylation damage, we have reconstituted the checkpoint response to MMS in Xenopus egg extracts. Using four different indicators for checkpoint activation (delay on entrance into mitosis, slowing of DNA replication, phosphorylation of the Chk1 protein, and physical association of the Rad17 checkpoint protein with damaged DNA), we report that MMS-induced checkpoint activation is dependent upon entrance into S phase. Additionally, we show that the replication of damaged double-stranded DNA, and not replication of damaged single-stranded DNA, is the molecular event that activates the checkpoint. Therefore, these data provide direct evidence that replication forks are an obligate intermediate in the activation of the DNA damage checkpoint.

PubMed ID: 12213834
PMC ID: PMC2173144
Article link: J Cell Biol
Grant support: [+]
Genes referenced: chek1 gem gmnn rad17 tbx2


Article Images: [+] show captions
References [+] :
Abraham, Cell cycle checkpoint signaling through the ATM and ATR kinases. 2001, Pubmed


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