Hijacking of the mismatch repair system to cause CAG expansion and cell death in neurodegenerative disease

被引:65
作者
McMurray, Cynthia T. [1 ,2 ]
机构
[1] Mayo Clin, Dept Mol Pharmacol & Expt Therapeut, Rochester, MN 55905 USA
[2] Mayo Clin, Dept Biochem & Mol Biol, Rochester, MN 55905 USA
关键词
mismatch repair; MSH2; MSH3; MSH6; DNA repair; microsatellite instability; trinucleotide repeats; CAG repeats; CTG repeats; base excision repair; break repair; OGG1; Huntington's disease; myotonic dystrophy; cisplatin lesions; DNA lesions; chemical lesions;
D O I
10.1016/j.dnarep.2008.03.013
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Mammalian cells have evolved sophisticated DNA repair systems to correct mispaired or damaged bases and extrahelical loops. Emerging evidence suggests that, in some cases, the normal DNA repair machinery is "hijacked" to become a causative factor in mutation and disease, rather than act as a safeguard of genomic integrity. In this review, we consider two cases in which active MMR leads to mutation or to cell death. There may be similar mechanisms by which uncoupling of normal MMR recognition from downstream repair allows triplet expansions underlying human neurodegenerative disease, or cell death in response to chemical lesion. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:1121 / 1134
页数:14
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