Leber’s hereditary optic neuropathy is associated with mitochondrial ND6 T14502C mutation |
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Authors: | Fuxin Zhao Minqiang Guan Xiangtian Zhou Meixia Yuan Ming Liang Qi Liu Yongmei Zhang Li Yang Qi-Ping Wei Jia Qu Min-Xin Guan |
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Institution: | a School of Ophthalmology and Optometry, Wenzhou Medical College, Wenzhou, Zhejiang 325003, China b Zhejiang Provincial Key Laboratory of Medical Genetics, School of Life Sciences, Wenzhou Medical College, Wenzhou, Zhejiang 325003, China c Division of Human Genetics, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH 45229, USA d The First Affiliated Hospital, Fujian Medical University, Fuzhou, Fujian 350005, China e Department of Ophthalmology, Dongfang Hospital, Beijing University of Chinese Medicine and Pharmacology, Beijing 100078, China f Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH 45229, USA |
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Abstract: | We report here the clinical, genetic, and molecular characterization of three Chinese families with Leber’s hereditary optic neuropathy (LHON). There were variable severity and age of onset in visual impairment among these families. Strikingly, there were extremely low penetrances of visual impairment in these Chinese families. Sequence analysis of complete mitochondrial genomes in these pedigrees showed the homoplasmic T14502C (I58V) mutation, which localized at a highly conserved isoleucine at position 58 of ND6, and distinct sets of mtDNA polymorphisms belonging to haplogroups M10a, F1a1, and H2. The occurrence of T14502C mutation in these several genetically unrelated subjects affected by visual impairment strongly indicates that this mutation is involved in the pathogenesis of visual impairment. Here, mtDNA variants I187T in the ND1, A122V in CO1, S99A in the A6, and V254I in CO3 exhibited an evolutionary conservation, indicating a potential modifying role in the development of visual impairment associated with T14502C mutation in those families. Furthermore, nuclear modifier gene(s) or environmental factor(s) may play a role in the phenotypic manifestation of the LHON-associated T14502C mutation in these Chinese families. |
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Keywords: | Mitochondrial DNA ND6 Mutation Leber&rsquo s hereditary optic neuropathy Visual loss Penetrance Haplogroup Maternally Chinese |
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