MRE11/RAD50/NBS1: complex activities

被引:105
作者
Assenmacher, N [1 ]
Hopfner, KP [1 ]
机构
[1] Univ Munich, Gene Ctr, D-81377 Munich, Germany
关键词
ABC : ATP binding cassette; AT : Ataxia telangiectasia; ATM : Ataxia telangiectasia mutated; DSB : DNA double-strand break; dsDNA : double-strand DNA; ssDNA : single-strand DNA; HR : homologous recombination; NBS : Nijmegen breakage syndrome; NHEJ : non-homologous end joining; WS : Werner syndrome;
D O I
10.1007/s00412-004-0306-4
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
The MRE11/RAD50/NBS1 complex (Mre11 complex) is a central player in most aspects of the cellular response to DNA double-strand breaks, including homologous recombination, non-homologous end joining, telomere maintenance and DNA damage checkpoint activation. Several of these findings are explained by the unusual enzymatic activities and macromolecular structure of the Mre11 complex. The Mre11 complex possesses an ATP-stimulated nuclease to process heterogeneous DNA ends and long coiled-coil tails to link DNA ends and/or sister chromatids. However, the mechanistic role of the Mre11 complex in checkpoint activation has been unclear until recently. New data suggest that the Mre11 complex can directly activate the ATM checkpoint kinase at DNA breaks. These findings, together with newly determined functional interactions, identify the Mre11 complex as an architectural and mechanistic keystone of cellular response events emerging from DNA breaks.
引用
收藏
页码:157 / 166
页数:10
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