Li Lei, Zou Lee
Department of Experimental Radiation Oncology, The University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA.
J Cell Biochem. 2005 Feb 1;94(2):298-306. doi: 10.1002/jcb.20355.
The DNA damage and replication checkpoints are signaling mechanisms that regulate and coordinate cellular responses to genotoxic conditions. Unlike typical signal transduction mechanisms that respond to one or a few stimuli, checkpoints can be activated by a broad spectrum of extrinsically or intrinsically derived DNA damage or replication interference. Recent investigations have shed light on how the damage and replication checkpoints are able to respond to such diverse stimuli. The activation of checkpoints not only attenuates cell cycle progression but also facilitates DNA repair and recovery of faltered replication forks, thereby preventing DNA lesions from being converted to inheritable mutations. Recently, more checkpoint targets from the cell cycle and DNA replication apparatus have been identified, revealing the increasing complexity of the checkpoint control of the cell cycle. In this article, we discuss current models of the DNA damage and replication checkpoints and highlight recent advances in the field.
DNA损伤和复制检查点是调节和协调细胞对基因毒性条件反应的信号传导机制。与响应一种或几种刺激的典型信号转导机制不同,检查点可被多种外在或内在来源的DNA损伤或复制干扰激活。最近的研究揭示了损伤和复制检查点如何能够响应如此多样的刺激。检查点的激活不仅会减弱细胞周期进程,还会促进DNA修复和停滞复制叉的恢复,从而防止DNA损伤转化为可遗传的突变。最近,已从细胞周期和DNA复制装置中鉴定出更多的检查点靶点,这揭示了细胞周期检查点控制的复杂性日益增加。在本文中,我们讨论了DNA损伤和复制检查点的当前模型,并强调了该领域的最新进展。