The molecular basis of muscular dystrophy in the mdx mouse: a point mutation

Sicinski, P; Geng, Y; Ryder-Cook, AS; Barnard, EA; Darlison, MG; Barnard, PJ

Abstract

The mdx mouse is an X-linked myopathic mutant, an animal model for human Duchenne muscular dystrophy. In both mouse and man the mutations lie within the dystrophin gene, but the phenotypic differences of the disease in the two species confer much interest on the molecular basis of the mdx mutation. The complementary DNA for mouse dystrophin has been cloned, and the sequence has been used in the polymerase chain reaction to amplify normal and mdx dystrophin transcripts in the area of the mdx mutation. Sequence analysis of the amplification products showed that the mdx mouse has a single base substitution within an exon, which causes premature termination of the polypeptide chain.

Citation

Sicinski, P., Geng, Y., Ryder-Cook, A., Barnard, E., Darlison, M., & Barnard, P. (1989). The molecular basis of muscular dystrophy in the mdx mouse: a point mutation. Science, 244(4912), 1578-1580. https://doi.org/10.1126/science.2662404

• Journal Article Type: Article
• Publication Date: Jun 30, 1989
• Deposit Date: Jul 27, 2016
• Journal: Science
• Print ISSN: 0036-8075
• Electronic ISSN: 1095-9203
• Publisher: American Association for the Advancement of Science
• Peer Reviewed: Peer Reviewed
• Volume: 244
• Issue: 4912
• Pages: 1578-1580
• DOI: https://doi.org/10.1126/science.2662404
• Keywords: Multidisciplinary
• Public URL: http://researchrepository.napier.ac.uk/Output/317375