DNA repair deficiency and neurological disease

被引:233
作者
McKinnon, Peter J. [1 ]
机构
[1] St Jude Childrens Hosp, Dept Genet & Tumour Cell Biol, Memphis, TN 38105 USA
来源
NATURE REVIEWS NEUROSCIENCE | 2009年 / 10卷 / 02期
基金
美国国家卫生研究院;
关键词
STRAND BREAK REPAIR; NUCLEOTIDE EXCISION-REPAIR; OCULAR MOTOR APRAXIA; CENTRAL-NERVOUS-SYSTEM; TRANSCRIPTION-COUPLED REPAIR; TELANGIECTASIA-LIKE DISORDER; EARLY EMBRYONIC LETHALITY; HEMATOPOIETIC STEM-CELLS; SUBSTANTIA-NIGRA NEURONS; HUMAN GENETIC-DISEASE;
D O I
10.1038/nrn2559
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The ability to respond to genotoxic stress is a prerequisite for the successful development of the nervous system. Mutations in various DNA repair factors can lead to human diseases that are characterized by pronounced neuropathology. In many of these syndromes the neurological component is among the most deleterious aspects of the disease. The nervous system poses a particular challenge in terms of clinical intervention, as the neuropathology associated with these diseases often arises during nervous system development and can be fully penetrant by childhood. Understanding how DNA repair deficiency affects the nervous system will provide a rational basis for therapies targeted at ameliorating the neurological problems in these syndromes.
引用
收藏
页码:100 / 112
页数:13
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