A subsynaptic protein of Mr approximately 300 kD is a major component of Torpedo electric organ postsynaptic membranes and copurifies with the AChR and the 43-kD subsynaptic protein. mAbs against this protein react with neuromuscular synapses in higher vertebrates, but not at synapses in dystrophic muscle. The Torpedo 300-kD protein comigrates in SDS-PAGE with murine dystrophin and reacts with antibodies against murine dystrophin. The sequence of a partial cDNA isolated by screening an expression library with mAbs against the Torpedo 300-kD protein shows striking homology to mammalian dystrophin, and in particular to the b isoform of dystrophin. These results indicate that dystrophin is a component of the postsynaptic membrane at neuromuscular synapses and raise the possibility that loss of dystrophin from synapses in dystrophic muscle may have consequences that contribute to muscular dystrophy.
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15 November 1991
Article|
November 15 1991
Dystrophin is a component of the subsynaptic membrane.
J E Yeadon,
J E Yeadon
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.
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H Lin,
H Lin
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.
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S M Dyer,
S M Dyer
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.
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S J Burden
S J Burden
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.
Search for other works by this author on:
J E Yeadon
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.
H Lin
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.
S M Dyer
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.
S J Burden
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.
Online ISSN: 1540-8140
Print ISSN: 0021-9525
J Cell Biol (1991) 115 (4): 1069–1076.
Citation
J E Yeadon, H Lin, S M Dyer, S J Burden; Dystrophin is a component of the subsynaptic membrane.. J Cell Biol 15 November 1991; 115 (4): 1069–1076. doi: https://doi.org/10.1083/jcb.115.4.1069
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