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PMID: 2481825 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Dystrophin distribution in heterozygote MDX mice.

Muscle & nerve ·Vol. 12 ·No. 10 ·1989-10-00 ·Pages 861-8

Watkins SC, Hoffman EP, Slayter HS, Kunkel LM

Abstract

The distribution of dystrophin in myofibers from normal, mdx hemizygous, and mdx heterozygous mice was studied at various times in development. While normal mice exhibit dystrophin immunostaining around the entire fiber periphery regardless of age, mdx hemizygous mice exhibit no staining (0-35 days). In contrast, young (10 day) heterozygous mdx mice showed neighboring dystrophin-negative and dystrophin-positive fibers as well as fibers with a discontinuous or patchy dystrophin labelling. Older heterozygotes displayed very few negative fibers, with most fibers exhibiting apparently complete dystrophin immunostaining. This, coupled with the absence of muscle fiber degeneration at any age point, and the apparently normal levels of dystrophin in older heterozygous mice, indicates that myonuclei containing the dystrophin gene can compensate for myonuclei which do not contain the dystrophin gene within the same myofiber.

MeSH Terms
Animals Dystrophin Fluorescent Antibody Technique Heterozygote Mice Mice, Inbred C57BL Muscle Proteins/analysis Muscles/analysis Muscular Dystrophy, Animal/metabolism Staining and Labeling
Chemicals
Dystrophin Muscle Proteins
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Watkins S C
Laboratory of Structural Molecular Biology, Dana-Farber Cancer Institute, Boston, MA 02115.
Hoffman E P
Slayter H S
Kunkel L M
Article Info
Journal
Muscle & nerve
Abbr.
Muscle Nerve
ISSN
0148-639X
Published
1989-10-00
Pages
861-8
Language
English
Region
United States
NLM ID
7803146
Subset
IM
Grants
NIGMS NIH HHS · GM14237 · United States
NINDS NIH HHS · NS23740 · United States
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