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.
机构:
Tabriz Univ Med Sci, Imam Reza Hosp, Neurosci Res Ctr, Tabriz, IranTabriz Univ Med Sci, Imam Reza Hosp, Neurosci Res Ctr, Tabriz, Iran
Andalib, Sasan
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h-index:
机构:
Talebi, Mahnaz
;
Sakhinia, Ebrahim
论文数: 0引用数: 0
h-index: 0
机构:
Univ Manchester, Fac Med & Human Sci, Sch Med, Div Regenerat Med, Manchester M13 9PL, Lancs, England
Tabriz Univ Med Sci, Dept Med Genet, Fac Med, Tabriz, IranTabriz Univ Med Sci, Imam Reza Hosp, Neurosci Res Ctr, Tabriz, Iran
机构:
Tabriz Univ Med Sci, Imam Reza Hosp, Neurosci Res Ctr, Tabriz, IranTabriz Univ Med Sci, Imam Reza Hosp, Neurosci Res Ctr, Tabriz, Iran
Andalib, Sasan
;
论文数: 引用数:
h-index:
机构:
Talebi, Mahnaz
;
Sakhinia, Ebrahim
论文数: 0引用数: 0
h-index: 0
机构:
Univ Manchester, Fac Med & Human Sci, Sch Med, Div Regenerat Med, Manchester M13 9PL, Lancs, England
Tabriz Univ Med Sci, Dept Med Genet, Fac Med, Tabriz, IranTabriz Univ Med Sci, Imam Reza Hosp, Neurosci Res Ctr, Tabriz, Iran