Association of a citrate synthase missense mutation with age-related hearing loss in A/J mice

Neurobiol Aging. 2012 Aug;33(8):1720-9. doi: 10.1016/j.neurobiolaging.2011.05.009. Epub 2011 Jul 30.

Abstract

We previously mapped a locus (ahl4) on distal Chromosome 10 that contributes to the age-related hearing loss of A/J strain mice. Here, we report on a refined genetic map position for ahl4 and its association with a mutation in the citrate synthase gene (Cs). We mapped ahl4 to the distal-most 7 megabases (Mb) of chromosome 10 by analysis of a new linkage backcross and then further narrowed the interval to 5.5 Mb by analysis of 8 C57BL/6J congenic lines with different A/J-derived segments of chromosome 10. A nucleotide variant in exon 3 of Cs is the only known DNA difference within the ahl4 candidate gene interval that is unique to the A/J strain and that causes a nonsynonymous codon change. Multiple lines of evidence implicate this missense mutation (H55N) as the underlying cause of ahl4-related hearing loss, likely through its effects on mitochondrial adenosine trisphosphate (ATP) and free radical production in cochlear hair cells. The A/J mouse thus provides a new model system for in vivo studies of mitochondrial function and hearing loss.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Aging / genetics*
  • Animals
  • Citrate (si)-Synthase / genetics*
  • Genetic Association Studies
  • Genetic Linkage / genetics*
  • Hearing Loss / genetics*
  • Mice
  • Mutation, Missense / genetics*
  • Polymorphism, Single Nucleotide / genetics*

Substances

  • Citrate (si)-Synthase