Oldies but Goldies mtDNA Population Variants and Neurodegenerative Diseases

被引:53
作者
Chinnery, Patrick F. [1 ,2 ]
Gomez-Duran, Aurora [1 ,2 ]
机构
[1] Univ Cambridge, Sch Clin Med, Dept Clin Neurosci, Cambridge, England
[2] MRC, Mitochondrial Biol Unit, Cambridge Biomed Campus, Cambridge, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
mtDNA; haplogroups; PD; LHON; neurodegenerative diseases; HEREDITARY OPTIC NEUROPATHY; MITOCHONDRIAL-DNA HAPLOGROUPS; CYBRID CELL-LINES; AMYOTROPHIC-LATERAL-SCLEROSIS; PARKINSONS-DISEASE; MULTIPLE-SCLEROSIS; OXIDATIVE-PHOSPHORYLATION; PHYLOGENETIC ANALYSIS; ALZHEIMERS-DISEASE; SPANISH POPULATION;
D O I
10.3389/fnins.2018.00682
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
mtDNA is transmitted through the maternal line and its sequence variability, which is population specific, is assumed to be phenotypically neutral. However, several studies have shown associations between the variants defining some genetic backgrounds and the susceptibility to several pathogenic phenotypes, including neurodegenerative diseases. Many of these studies have found that some of these variants impact many of these phenotypes, including the ones defining the Caucasian haplogroups H, J, and Uk, while others, such as the ones defining the T haplogroup, have phenotype specific associations. In this review, we will focus on those that have shown a pleiotropic effect in population studies in neurological diseases. We will also explore their bioenergetic and genomic characteristics in order to provide an insight into the role of these variants in disease. Given the importance of mitochondrial population variants in neurodegenerative diseases a deeper analysis of their effects might unravel new mechanisms of disease and help design new strategies for successful treatments.
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页数:11
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