The Mre11 complex and the metabolism of chromosome breaks: the importance of communicating and holding things together

被引:211
作者
Stracker, TH
Theunissen, JWF
Morales, M
Petrini, JHJ [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Program Mol Biol, New York, NY 10021 USA
[2] Cornell Univ, Grad Sch Med Sci, New York, NY 10021 USA
关键词
Mre11; complex; double strand breaks; checkpoints; ATM;
D O I
10.1016/j.dnarep.2004.03.014
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The conserved Mre11 complex (Mre11, Rad50, and Nbs1) plays a role in each aspect of chromosome break metabolism. The complex acts as a break sensor and functions in the activation and propagation of signaling pathways that govern cell cycle checkpoint functions in response to DNA damage. In addition, the Mre11 complex influences recombinational DNA repair through promoting recombination between sister chromatids. The Mre11 complex is required for mammalian cell viability but hypomorphic Mutants of Mre11 and Nbs1 have been identified in human genetic instability disorders. These hypomorphic mutations, as well as those identified in yeast, have provided a benchmark for establishing mouse models of Mre11 complex deficiency. In addition to consideration of Mre11 complex functions in human cells and yeast, this review will discuss the characterization of mouse models and insight gleaned from those models regarding the metabolism of chromosome breaks. The current picture of break metabolism Supports a central role for the Mre11 complex at the interface of chromosome stability and the regulation of cell growth. Further genetic analysis of the Mre11 complex will be an invaluable tool for dissecting its function on an organismal level and determining its role in the prevention of malignancy. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:845 / 854
页数:10
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