Friedel Anna M, Pike Brietta L, Gasser Susan M
Friedrich Miescher Institute for Biomedical Research, Basel, Switzerland.
Curr Opin Cell Biol. 2009 Apr;21(2):237-44. doi: 10.1016/j.ceb.2009.01.017. Epub 2009 Feb 21.
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.
在S期,真核细胞解开并复制大量DNA,生成对内源和外源损伤都非常敏感的结构。DNA聚合酶与受损DNA或其他阻碍叉状结构进展的物质发生碰撞会产生复制应激,如果复制体组件不稳定,这种应激可能会演变成叉状结构崩溃。为确保基因组完整性,停滞的复制叉由一个检查点识别,其核心成分是人类激酶ATR或酿酒酵母中的Mec1。本综述将讨论最近的研究发现,揭示ATR/Mec1激酶的作用:既直接稳定复制体,又激活检查点反应以调节起始点激发、DNA修复、叉状结构重启和细胞周期进程。