共 118 条
Regulation of the cellular DNA double-strand break response
被引:78
作者:

Cann, Kendra L.
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h-index: 0
机构:
Univ Manitoba, Manitoba Inst Cell Biol, Winnipeg, MB R3E 0V9, Canada Univ Manitoba, Manitoba Inst Cell Biol, Winnipeg, MB R3E 0V9, Canada

Hicks, Geoffrey G.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Manitoba, Manitoba Inst Cell Biol, Winnipeg, MB R3E 0V9, Canada Univ Manitoba, Manitoba Inst Cell Biol, Winnipeg, MB R3E 0V9, Canada
机构:
[1] Univ Manitoba, Manitoba Inst Cell Biol, Winnipeg, MB R3E 0V9, Canada
来源:
BIOCHEMISTRY AND CELL BIOLOGY-BIOCHIMIE ET BIOLOGIE CELLULAIRE
|
2007年
/
85卷
/
06期
关键词:
DNA double-strand breaks;
cell-cycle checkpoints;
apoptosis;
DNA repair;
gamma radiation;
D O I:
10.1139/O07-135
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:
DNA double-strand breaks occur frequently in cycling cells, and are also induced by exogenous sources, including ionizing radiation. Cells have developed integrated double-strand break response pathways to cope with these lesions, including pathways that initiate DNA repair (either via homologous recombination or nonhomologous end joining), the cell-cycle checkpoints (G(1)-S, intra-S phase, and G(2)-M) that provide time for repair, and apoptosis. However, before any of these pathways can be activated, the damage must first be recognized. In this review, we will discuss how the response of mammalian cells to DNA double-strand breaks is regulated, beginning with the activation of ATM, the pinnacle kinase of the double-strand break signalling cascade.
引用
收藏
页码:663 / 674
页数:12
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