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Curr Opin Cell Biol. 2009 Apr;21(2):237-44. doi: 10.1016/j.ceb.2009.01.017. Epub 2009 Feb 21.

ATR/Mec1: coordinating fork stability and repair.

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1
Friedrich Miescher Institute for Biomedical Research, Basel, Switzerland.

Abstract

During S phase, eukaryotic cells unwind and duplicate a tremendous amount of DNA, generating structures that are very sensitive to both endogenous and exogenous insults. The collision of DNA polymerases with damaged DNA or other obstructions to fork progression generates replication stress, which can evolve into fork collapse if the replisome components are not stabilized. To ensure genome integrity, stalled replication forks are recognized by a checkpoint, whose central player is the human kinase ATR or Mec1 in S. cerevisiae. This review will discuss recent findings revealing roles of the ATR/Mec1 kinase: both in stabilizing the replisome directly and in activating the checkpoint response to regulate origin firing, DNA repair, fork restart, and cell cycle progression.

PMID:
19230642
DOI:
10.1016/j.ceb.2009.01.017
[Indexed for MEDLINE]
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