Genome integrity and disease prevention in the nervous system

被引:109
|
作者
McKinnon, Peter J. [1 ]
机构
[1] St Jude Childrens Res Hosp, Dept Genet, 332 N Lauderdale St, Memphis, TN 38105 USA
基金
美国国家卫生研究院;
关键词
DNA damage; nervous system; genome stability; neurodevelopment; neurologic disease; STRAND BREAK REPAIR; HUMAN POLYNUCLEOTIDE KINASE; AICARDI-GOUTIERES-SYNDROME; BASE EXCISION-REPAIR; TRANSCRIPTIONAL PAUSE SITES; EARLY EMBRYONIC LETHALITY; ENDOGENOUS DNA-DAMAGE; OCULAR MOTOR APRAXIA; ATM PROTEIN-KINASE; ATAXIA-TELANGIECTASIA;
D O I
10.1101/gad.301325.117
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Multiple DNA repair pathways maintain genome stability and ensure that DNA remains essentially unchanged over the life of a cell. Various human diseases occur if DNA repair is compromised, and most of these impact the nervous system, in some cases exclusively. However, it is often unclear what specific endogenous damage underpins disease pathology. Generally, the types of causative DNA damage are associated with replication, transcription, or oxidative metabolism; other direct sources of endogenous lesions may arise from aberrant topoisomerase activity or ribonucleotide incorporation into DNA. This review focuses on the etiology of DNA damage in the nervous system and the genome stability pathways that prevent human neurologic disease.
引用
收藏
页码:1180 / 1194
页数:15
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