Analysis of mitochondrial DNA variations in a Chinese family with spinocerebellar ataxia

Aiping Zeng, Xinwei Liu, Lijun Shen, Weizhen Li, Zhongying Ding, Yidong Bai, Jianxin Lu

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Abstract

Mitochondrial dysfunction and mitochondrial DNA (mtDNA) variations have been shown to have a role in several neurological diseases. To determine whether there is an association between mtDNA variations and spinocerebellar ataxia (SCA), we analyzed the mtDNA main control region (D-loop), as well as mtDNA content and the prevalence of the common deletion, in blood samples from members of a large Chinese family (14 individuals with SCA and 13 healthy individuals). All 14 individuals with SCA were genotyped as SCA3. Thirteen mtDNA haplotypes were identified among the 27 subjects. We detected no mutations in the mtDNA D-loop region and found no significant differences in mtDNA copy number or common deletion level between patients and their healthy relatives. Contrary to some previous reports, our study showed that mtDNA variations seem to be a rare event in individuals with SCA3.

Original languageEnglish (US)
Pages (from-to)60-64
Number of pages5
JournalJournal of Clinical Neuroscience
Volume19
Issue number1
DOIs
StatePublished - Jan 1 2012

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Keywords

  • Chinese family
  • Haplotype
  • Mitochondrial DNA
  • Spinocerebellar ataxia

ASJC Scopus subject areas

  • Surgery
  • Neurology
  • Clinical Neurology
  • Physiology (medical)

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