The homologue of the Duchenne locus is defective in X-linked muscular dystrophy of dogs

Nature. 1988 Jul 14;334(6178):154-6. doi: 10.1038/334154a0.


Duchenne muscular dystrophy (DMD) is the most common and the most severe of the muscular dystrophies in man. It is inherited as an X-linked recessive trait and is characterized by ongoing necrosis of skeletal muscle fibres with regeneration and eventually fibrosis and fatty infiltration. Although the gene and gene product which are defective in DMD have recently been identified, the pathogenesis of the disease is still poorly understood. A myopathy has been described in the dog which has been shown to be inherited as an X-linked trait and which is therefore a potential model of the human disease. We have studied the phenotypic expression of the disease, canine X-linked muscular dystrophy (CXMD), and have examined the molecular relationship between it and DMD. We report here that dogs with CXMD faithfully mimic the phenotype of Duchenne muscular dystrophy and that they lack the Duchenne gene transcript and its protein product, dystrophin.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Dogs / genetics*
  • Dystrophin
  • Immunosorbent Techniques
  • Muscle Proteins / genetics*
  • Muscle Proteins / immunology
  • Muscular Dystrophy, Animal / genetics*
  • Muscular Dystrophy, Animal / pathology
  • X Chromosome


  • Dystrophin
  • Muscle Proteins