The Repeat Expansion Diseases: The dark side of DNA repair

被引:47
|
作者
Zhao, Xiao-Nan [1 ]
Usdin, Karen [1 ]
机构
[1] Natl Inst Diabet Digest & Kidney Dis, Sect Genom Struct & Funct, Lab Cell & Mol Biol, NIH, Bethesda, MD 20892 USA
关键词
Repeat Expansion Diseases; Mismatch repair; Base excision repair; Transcription coupled repair; Global genome repair; Oxidative damage; BASE EXCISION-REPAIR; DOMINANT CEREBELLAR-ATAXIA; TRANSCRIPTION-COUPLED REPAIR; MYOTONIC-DYSTROPHY TYPE-2; CAG TRINUCLEOTIDE REPEAT; KNOCK-IN MICE; SPINOCEREBELLAR ATAXIA; TRIPLET-REPEAT; MISMATCH-REPAIR; CTG REPEAT;
D O I
10.1016/j.dnarep.2015.04.019
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
DNA repair normally protects the genome against mutations that threaten genome integrity and thus cell viability. However, growing evidence suggests that in the case of the Repeat Expansion Diseases, disorders that result from an increase in the size of a disease-specific microsatellite, the disease-causing mutation is actually the result of aberrant DNA repair. A variety of proteins from different DNA repair pathways have thus far been implicated in this process. This review will summarize recent findings from patients and from mouse models of these diseases that shed light on how these pathways may interact to cause repeat expansion. Published by Elsevier B.V.
引用
收藏
页码:96 / 105
页数:10
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