A nuclear-mitochondrial DNA interaction affecting hearing impairment in mice

Nat Genet. 2001 Feb;27(2):191-4. doi: 10.1038/84831.


The pathophysiologic pathways and clinical expression of mitochondrial DNA (mtDNA) mutations are not well understood. This is mainly the result of the heteroplasmic nature of most pathogenic mtDNA mutations and of the absence of clinically relevant animal models with mtDNA mutations. mtDNA mutations predisposing to hearing impairment in humans are generally homoplasmic, yet some individuals with these mutations have severe hearing loss, whereas their maternal relatives with the identical mtDNA mutation have normal hearing. Epidemiologic, biochemical and genetic data indicate that nuclear genes are often the main determinants of these differences in phenotype. To identify a mouse model for maternally inherited hearing loss, we screened reciprocal backcrosses of three inbred mouse strains, A/J, NOD/LtJ and SKH2/J, with age-related hearing loss (AHL). In the (A/J x CAST/Ei) x A/J backcross, mtDNA derived from the A/J strain exerted a significant detrimental effect on hearing when compared with mtDNA from the CAST/Ei strain. This effect was not seen in the (NOD/LtJ x CAST/Ei) x NOD/LtJ and (SKH2/J x CAST/Ei) x SKH2/J backcrosses. Genotyping revealed that this effect was seen only in mice homozygous for the A/J allele at the Ahl locus on mouse chromosome 10. Sequencing of the mitochondrial genome in the three inbred strains revealed a single nucleotide insertion in the tRNA-Arg gene (mt-Tr) as the probable mediator of the mitochondrial effect. This is the first mouse model with a naturally occurring mtDNA mutation affecting a clinical phenotype, and it provides an experimental model to dissect the pathophysiologic processes connecting mtDNA mutations to hearing loss.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Age Factors
  • Animals
  • Base Sequence
  • Cell Nucleus / genetics*
  • Crosses, Genetic
  • DNA, Mitochondrial / genetics*
  • Deafness / genetics*
  • Evoked Potentials, Auditory / genetics
  • Evolution, Molecular
  • Mice
  • Mice, Inbred Strains
  • Mitochondria / genetics*
  • Molecular Sequence Data
  • Nucleic Acid Conformation
  • Point Mutation
  • RNA, Transfer, Arg / genetics
  • Sequence Homology, Nucleic Acid


  • DNA, Mitochondrial
  • RNA, Transfer, Arg

Associated data

  • GENBANK/L07095
  • GENBANK/L07096