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Title: The coexistence of mitochondrial ND6 T14484C and 12S rRNA A1555G mutations in a Chinese family with Leber's hereditary optic neuropathy and hearing loss

Journal Article · · Biochemical and Biophysical Research Communications
OSTI ID:20991386
 [1];  [2];  [3];  [1];  [1];  [3];  [3];  [2];  [2];  [4]
  1. Department of Ophthalmology, Dongfang Hospital, Beijing University of Chinese Medicine and Pharmacology, Beijing 100078 (China)
  2. School of Ophthalmology and Optometry, Wenzhou Medical College, Wenzhou, Zhejiang 325003 (China)
  3. Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229 (United States)
  4. Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH 45229 (United States) and Zhejiang Provincial Key Laboratory of Medical Genetics, School of Life Sciences, Wenzhou Medical College, Wenzhou, Zhejiang 325003 (China) and Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH 45229 (United States)

We report here the clinical, genetic and molecular characterization of one three-generation Han Chinese family with Leber's hereditary optic neuropathy (LHON) and hearing loss. Four of 14 matrilineal relatives exhibited the moderate central vision loss at the average age of 12.5 years. Of these, one subject exhibited both LHON and mild hearing impairment. Sequence analysis of the complete mitochondrial genomes in the pedigree showed the presence of homoplasmic LHON-associated ND6 T14484C mutation, deafness-associated 12S rRNA A1555 mutation and 47 other variants belonging to Eastern Asian haplogroup H2. None of other mitochondrial variants was evolutionarily conserved and functional significance. Therefore, the coexistence of the A1555G mutation and T14484C mutations in this Chinese family indicate that the A1555G mutation may play a synergistic role in the phenotypic manifestation of LHON associated ND6 T14484C mutation. However, the incomplete penetrance of vision and hearing loss suggests the involvement of nuclear modifier genes and environmental factors in the phenotypic expression of these mtDNA mutations.

OSTI ID:
20991386
Journal Information:
Biochemical and Biophysical Research Communications, Vol. 357, Issue 4; Other Information: DOI: 10.1016/j.bbrc.2007.04.025; PII: S0006-291X(07)00735-8; Copyright (c) 2007 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved; Country of input: International Atomic Energy Agency (IAEA); ISSN 0006-291X
Country of Publication:
United States
Language:
English

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