Double-strand breaks: signaling pathways and repair mechanisms

被引:67
作者
Karagiannis, TC
El-Osta, A
机构
[1] Baker Med Res Inst, Alfred Med Res & Educ Precinct, Epigenet Human Hlth & Dis Lab, Prahran, Vic 3181, Australia
[2] Peter MacCallum Canc Ctr, Trescowthick Res Labs, Melbourne, Vic, Australia
关键词
DNA double-strand breaks; signal transduction; trancriptional responses; homologous recombination; non-homologous end-joining; chromatin remodeling;
D O I
10.1007/s00018-004-4174-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:2137 / 2147
页数:11
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