Karagiannis T C, El-Osta A
Molecular Radiation Biology, Trescowthick Research Laboratories, Peter MacCallum Cancer Centre, Melbourne, Australia.
Cell Mol Life Sci. 2004 Sep;61(17):2137-47. doi: 10.1007/s00018-004-4174-0.
Double-strand breaks arise frequently in the course of endogenous - normal and pathological - cellular DNA metabolism or can result from exogenous agents such as ionizing radiation. It is generally accepted that these lesions represent one of the most severe types of DNA damage with respect to preservation of genomic integrity. Therefore, cells have evolved complex mechanisms that include cell-cycle arrest, activation of various genes, including those associated with DNA repair, and in certain cases induction of the apoptotic pathway to respond to double-strand breaks. In this review we discuss recent progress in our understanding of cellular responses to DNA double-strand breaks. In addition to an analysis of the current paradigms of detection, signaling and repair, insights into the significance of chromatin remodeling in the double-strand break-response pathways are provided.
双链断裂在内源性(正常和病理)细胞DNA代谢过程中频繁出现,也可能由诸如电离辐射等外源性因素导致。人们普遍认为,就基因组完整性的维持而言,这些损伤代表了最严重的DNA损伤类型之一。因此,细胞进化出了复杂的机制,包括细胞周期停滞、激活各种基因(包括与DNA修复相关的基因),以及在某些情况下诱导凋亡途径来应对双链断裂。在这篇综述中,我们讨论了我们对细胞对DNA双链断裂反应的理解方面的最新进展。除了分析检测、信号传导和修复的当前范式外,还提供了对染色质重塑在双链断裂反应途径中的重要性的见解。