Journal Article

Null mutation of calpain 3 (p94) in mice causes abnormal sarcomere formation <i>in vivo</i> and <i>in vitro</i>

I. Kramerova, E. Kudryashova, J.G. Tidball and Melissa J. Spencer

in Human Molecular Genetics

Volume 13, issue 13, pages 1373-1388
Published in print July 2004 | ISSN: 0964-6906
Published online May 2004 | e-ISSN: 1460-2083 | DOI: http://dx.doi.org/10.1093/hmg/ddh153
Null mutation of calpain 3 (p94) in mice causes abnormal sarcomere formation in vivo and in vitro

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The giant protein titin serves a primary role as a scaffold for sarcomere assembly; however, proteins that mediate this remodeling have not been identified. One potential mediator of this process is the protease calpain 3 (C3), the protein mutated in limb girdle muscular dystrophy type 2A. To test the hypothesis that C3 mediates remodeling during myofibrillogenesis, C3 knockout (C3KO) mice were generated. The C3KO mice were atrophic containing small foci of muscular necrosis. Myogenic cells fused normally in vitro, but lacked well-organized sarcomeres, as visualized by electron microscopy (EM). Titin distribution was normal in longitudinal sections from the C3KO mice; however, EM of muscle fibers showed misaligned A-bands. In vitro studies revealed that C3 can bind and cleave titin and that some mutations that are pathogenic in human muscular dystrophy result in reduced affinity of C3 for titin. These studies suggest a role for C3 in myofibrillogenesis and sarcomere remodeling.

Journal Article.  9684 words.  Illustrated.

Subjects: Genetics and Genomics

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