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Regional localization of the murine Duchenne muscular dystrophy gene on the mouse X chromosome
Authors:Jeffrey S. Chamberlain  Stephen G. Grant  Alice A. Reeves  Linda J. Mullins  Dennis A. Stephenson  Eric P. Hoffman  Anthony P. Monaco  Louis M. Kunkel  C. Thomas Caskey  Verne M. Chapman
Affiliation:(1) Institute for Molecular Genetics, Baylor College of Medicine, One Baylor Plaza, 77030 Houston, Texas;(2) New York State Department of Health, Roswell Park Memorial Institute, 14263 Buffalo, New York;(3) Division of Genetics, Department of Pediatrics, Harvard Medical School Children's Hospital, 02115 Boston, Massachusetts;(4) The Program in Neuroscience, Harvard University, 02138 Cambridge, Massachusetts
Abstract:The murine locus corresponding to the human Duchenne/Becker muscular dystrophy (DMD) gene has been regionally mapped on the mouse X chromosome by hybridizing DNA from interspecies mouse crosses with a cDNA clone for the mouse Dmd gene. The results demonstrate that the relative organization of genes on the murine and human X chromosomes is more divergent than has previously been postulated. Furthermore, the mouse Dmd gene maps to a similar region of the X chromosome as does the mouse muscular dystrophy mutation mdx, providing further evidence that the mdx mutant may be a murine equivalent of human DMD. However, Southern analysis of portions of the mouse Dmd gene has not yet revealed any differences between mdx and wild-type mice.
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