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XB-ART-38987
Mol Cell 2008 Dec 26;326:862-9. doi: 10.1016/j.molcel.2008.12.005.
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The role of Dbf4/Drf1-dependent kinase Cdc7 in DNA-damage checkpoint control.

Tsuji T , Lau E , Chiang GG , Jiang W .


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The Dbf4/Drf1-dependent S-phase-promoting kinase Cdc7 (Ddk) is thought to be an essential target inactivated by the S-phase checkpoint machinery that inhibits DNA replication. However, we show here that the complex formation, chromatin association, and kinase activity of Ddk are not inhibited during the DNA-damage-induced S-phase checkpoint response in Xenopus egg extracts and mammalian cells. Instead, we find that Ddk plays an active role in regulating S-phase checkpoint signaling. Addition of purified Ddk to Xenopus egg extracts or overexpression of Dbf4 in HeLa cells downregulates ATR-Chk1 checkpoint signaling and overrides the inhibition of DNA replication and cell-cycle progression induced by DNA-damaging agents. These results indicate that Ddk functions as an upstream regulator to monitor S-phase checkpoint signaling. We propose that Ddk modulates the S-phase checkpoint control by attenuating checkpoint signaling and triggering DNA replication reinitiation during the S-phase checkpoint recovery.

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Species referenced: Xenopus
Genes referenced: atr cdc7 chek1 dbf4 dbf4b diaph1

References [+] :
Aparicio, Components and dynamics of DNA replication complexes in S. cerevisiae: redistribution of MCM proteins and Cdc45p during S phase. 1997, Pubmed