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Dystrophin and Utrophin Complexed with Different Associated Proteins in Cardiac Purkinje Fibres
Authors:François Rivier  Agnès Robert  Gérald Hugon  Armelle Bonet-Kerrache  Vincenzo Nigro  Jean-Alain Fehrentz  Jean Martinez and Dominique Mornet
Institution:(1) Muscles and Pathologies, INSERM U18, 1FR24, 1919 Route de Monde, 34293 Montpellier Cedex 5, France;(2) Istituto di Patologia generale ed Oncologia, Facoltà di Medicina e Chirurgia, Largo Sant' Aniello a Caponapoli, 2, I-80138 Napoli, Italy;(3) Laboratoire des Aminoacides, peptides et Protéines, Universités de MontpellierI et II, Faculté de Pharmacie, LAPP, ESA CNRS 5075, 34060 Montpellier, CEDEX, France
Abstract:Abnormal dystrophin expression is directly responsible for Duchenne and Becker muscular dystrophies. In skeletal muscle, dystrophin provides a link between the actin network and the extracellular matrix via the dystrophin-associated protein complex. In mature skeletal muscle, utrophin is a dystrophin-related protein localized mainly at the neuromuscular junction, with the same properties as dystrophin in terms of linking the protein complex. Utrophin could potentially overcome the absence of dystrophin in dystrophic skeletal muscles. In cardiac muscle, dystrophin and utrophin were both found to be present with a distinct subcellular distribution in Purkinje fibres, i.e. utrophin was limited to the cytoplasm, while dystrophin was located in the cytoplasmic membrane.In this study, we used this particular characteristic of cardiac Purkinje fibres and demonstrated that associated proteins of dystrophin and utrophin are different in this structure. We conclude, contrary to skeletal muscle, dystrophin-associated proteins do not form a complex in Purkinje fibres. In addition, we have indirect evidence of the presence of two different 400thinspkDa dystrophins in Purkinje fibres.
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