The two edges of the ATM sword:: Co-operation between repair and checkpoint functions

被引:63
作者
Löbrich, M
Jeggo, PA
机构
[1] Univ Saarland, Fachrichtung Biophys, D-66421 Homburg, Germany
[2] Univ Sussex, Genome Damage & Stabil Ctr, Brighton BN1 9RH, E Sussex, England
关键词
DNA double strand breaks; signal transduction; ionising radiation; radiosensitivity; ataxia telagiectasia; artemis;
D O I
10.1016/j.radonc.2005.06.027
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
ATM is a central component of a signal transduction process that responds to DNA double strand breaks (DSBs) ultimately effecting cell cycle checkpoint arrest and/or apoptosis. Recent studies have shown that ATM also regulates a mechanism of processing a subset of DNA ends that appear to be difficult to ligate, since they are rejoined with slow kinetics in control cells. In the absence of this process, which involves the nuclease, Artemis, the DSBs either remain unrejoined or potentially undergo misrejoining. Thus, ATM's checkpoint function specifically facilitates its repair function. Here, we discuss the contribution of this novel function of ATM to survival after ionising irradiation and to cancer avoidance. We suggest that ATM's strength as a damage response protein lies in the co-ordination of its repair and checkpoint functions making a razor sharp knife out of two blunter edges. (C) 2005 Elsevier Ireland Ltd.
引用
收藏
页码:112 / 118
页数:7
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