Costanzo V, Robertson K, Ying C Y, Kim E, Avvedimento E, Gottesman M, Grieco D, Gautier J
Department of Genetics and Development, Columbia University, New York, NY 10032, USA.
Mol Cell. 2000 Sep;6(3):649-59. doi: 10.1016/s1097-2765(00)00063-0.
Cell cycle checkpoints lead to the inhibition of cell cycle progression following DNA damage. A cell-free system derived from Xenopus eggs has been established that reconstitutes the checkpoint pathway inhibiting DNA replication initiation. DNA containing double-strand breaks inhibits replication initiation in a dose-dependent manner. Upon checkpoint activation, a prereplicative complex is assembled that contains ORC, Cdc6, Cdc7, and MCM proteins but lacks Cdc45. The checkpoint is ATM dependent. Cdk2/CyclinE acts downstream of ATM and is downregulated by Cdk2 phosphorylation on tyrosine 15. Cdk2AF/CyclinE is refractory to checkpoint signaling, and Cdc25A overrides the checkpoint and restores DNA replication. This report provides the description of a DNA damage checkpoint pathway that prevents the onset of S phase independently of the transcriptional function of p53 in a vertebrate organism.
细胞周期检查点可导致DNA损伤后细胞周期进程的抑制。已建立了一种源自非洲爪蟾卵的无细胞系统,该系统可重建抑制DNA复制起始的检查点途径。含有双链断裂的DNA以剂量依赖的方式抑制复制起始。在检查点激活后,会组装一个前复制复合体,该复合体包含ORC、Cdc6、Cdc7和MCM蛋白,但缺乏Cdc45。该检查点依赖于ATM。Cdk2/细胞周期蛋白E在ATM下游起作用,并通过酪氨酸15上的Cdk2磷酸化而下调。Cdk2AF/细胞周期蛋白E对检查点信号不敏感,而Cdc25A可绕过检查点并恢复DNA复制。本报告描述了一种DNA损伤检查点途径,该途径可在脊椎动物中独立于p53的转录功能阻止S期的开始。