Please use this identifier to cite or link to this item: http://hdl.handle.net/1893/7180
Appears in Collections:Aquaculture Journal Articles
Peer Review Status: Refereed
Title: Dystrophin is required for the formation of stable muscle attachments in the zebrafish embryo
Authors: Bassett, D I
Bryson-Richardson, Robert J
Daggett, David F
Gautier, Philippe
Keenan, David G
Currie, Peter D
Contact Email: d.i.bassett@stir.ac.uk
Keywords: Myomuscular junctions
Myotendinous junctions
Dystrophin
Sapje
Muscle attachments
Muscular dystrophy
Congenital myopathy
Issue Date: Dec-2003
Publisher: Company of Biologists
Citation: Bassett DI, Bryson-Richardson RJ, Daggett DF, Gautier P, Keenan DG & Currie PD (2003) Dystrophin is required for the formation of stable muscle attachments in the zebrafish embryo, Development, 130 (23), pp. 5851-5860.
Abstract: A class of recessive lethal zebrafish mutations has been identified in which normal skeletal muscle differentiation is followed by a tissue-specific degeneration that is reminiscent of the human muscular dystrophies. Here, we show that one of these mutations, sapje, disrupts the zebrafish orthologue of the X-linked human Duchenne muscular dystrophy (DMD) gene. Mutations in this locus cause Duchenne or Becker muscular dystrophies in human patients and are thought to result in a dystrophic pathology through disconnecting the cytoskeleton from the extracellular matrix in skeletal muscle by reducing the level of dystrophin protein at the sarcolemma. This is thought to allow tearing of this membrane, which in turn leads to cell death. Surprisingly, we have found that the progressive muscle degeneration phenotype of sapje mutant zebrafish embryos is caused by the failure of embryonic muscle end attachments. Although a role for dystrophin in maintaining vertebrate myotendinous junctions (MTJs) has been postulated previously and MTJ structural abnormalities have been identified in the Dystrophin-deficient mdx mouse model, in vivo evidence of pathology based on muscle attachment failure has thus far been lacking. This zebrafish mutation may therefore provide a model for a novel pathological mechanism of Duchenne muscular dystrophy and other muscle diseases.
Type: Journal Article
URI: http://hdl.handle.net/1893/7180
URL: http://www.ncbi.nlm.nih.gov/pubmed/14573513
DOI Link: http://dx.doi.org/10.1242/dev.00799
Rights: Publisher policy is that the author retains copyright. Full publisher policy available at: http://dev.biologists.org/site/misc/rights_permissions.xhtml
Affiliation: Aquaculture (Machrihanish)
Victor Chang Cardiac Research Institute
University of California, Berkeley
Western General Hospital
Victor Chang Cardiac Research Institute
Victor Chang Cardiac Research Institute

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