Danish Centre for Molecular Gerontology and Danish Aging Research Center, University of Aarhus, Department of Molecular Biology, Aarhus, Denmark.
Prog Neurobiol. 2011 Jul;94(2):166-200. doi: 10.1016/j.pneurobio.2011.04.013. Epub 2011 Apr 30.
Deficiency in repair of nuclear and mitochondrial DNA damage has been linked to several neurodegenerative disorders. Many recent experimental results indicate that the post-mitotic neurons are particularly prone to accumulation of unrepaired DNA lesions potentially leading to progressive neurodegeneration. Nucleotide excision repair is the cellular pathway responsible for removing helix-distorting DNA damage and deficiency in such repair is found in a number of diseases with neurodegenerative phenotypes, including Xeroderma Pigmentosum and Cockayne syndrome. The main pathway for repairing oxidative base lesions is base excision repair, and such repair is crucial for neurons given their high rates of oxygen metabolism. Mismatch repair corrects base mispairs generated during replication and evidence indicates that oxidative DNA damage can cause this pathway to expand trinucleotide repeats, thereby causing Huntington's disease. Single-strand breaks are common DNA lesions and are associated with the neurodegenerative diseases, ataxia-oculomotor apraxia-1 and spinocerebellar ataxia with axonal neuropathy-1. DNA double-strand breaks are toxic lesions and two main pathways exist for their repair: homologous recombination and non-homologous end-joining. Ataxia telangiectasia and related disorders with defects in these pathways illustrate that such defects can lead to early childhood neurodegeneration. Aging is a risk factor for neurodegeneration and accumulation of oxidative mitochondrial DNA damage may be linked with the age-associated neurodegenerative disorders Alzheimer's disease, Parkinson's disease and amyotrophic lateral sclerosis. Mutation in the WRN protein leads to the premature aging disease Werner syndrome, a disorder that features neurodegeneration. In this article we review the evidence linking deficiencies in the DNA repair pathways with neurodegeneration.
核和线粒体 DNA 损伤修复缺陷与几种神经退行性疾病有关。许多最近的实验结果表明,有丝分裂后神经元特别容易积累未修复的 DNA 损伤,这可能导致进行性神经退行性变。核苷酸切除修复是负责清除螺旋扭曲 DNA 损伤的细胞途径,在包括着色性干皮病和 Cockayne 综合征在内的许多具有神经退行性表型的疾病中,都发现这种修复存在缺陷。修复氧化碱基损伤的主要途径是碱基切除修复,鉴于神经元的高代谢率,这种修复对神经元至关重要。错配修复纠正复制过程中产生的碱基错配,有证据表明,氧化 DNA 损伤可导致该途径扩展三核苷酸重复,从而导致亨廷顿病。单链断裂是常见的 DNA 损伤,与神经退行性疾病共济失调-眼动不能-口面运动障碍-1 和脊髓小脑共济失调伴轴索性神经病-1 有关。DNA 双链断裂是有毒的损伤,存在两种主要的修复途径:同源重组和非同源末端连接。共济失调毛细血管扩张症和相关疾病中这些途径的缺陷表明,这种缺陷可能导致儿童早期神经退行性变。衰老也是神经退行性变的一个风险因素,氧化线粒体 DNA 损伤的积累可能与与年龄相关的神经退行性疾病阿尔茨海默病、帕金森病和肌萎缩侧索硬化症有关。WRN 蛋白的突变导致早老病 Werner 综合征,这是一种以神经退行性变为特征的疾病。本文综述了 DNA 修复途径缺陷与神经退行性变之间的关联证据。