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Am J Physiol Cell Physiol 290: C711-C718, 2006. First published October 19, 2005; doi:10.1152/ajpcell.00217.2005
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MUSCLE CELL BIOLOGY AND CELL MOTILITY

Transition of Homer isoforms during skeletal muscle regeneration

Elena Bortoloso,1,2 Nadia Pilati,1 Aram Megighian,3 Elisa Tibaldo,1 Dorianna Sandonà,1 and Pompeo Volpe1,2

1Dipartimento di Scienze Biomediche Sperimentali dell'Università di Padova, 2Istituto Interuniversitario di Miologia, and 3Dipartimento di Anatomia e Fisiologia Umana dell'Università di Padova, Padova, Italy

Submitted 6 May 2005 ; accepted in final form 11 October 2005

Homer represents a new and diversified family of proteins that includes several isoforms, Homer 1, 2, and 3; some of these isoforms have been reported to be present in striated muscles. In this study, the presence of Homer isoforms 1a, 1b/c/d, 2b, and 3 was thoroughly investigated in rat skeletal muscles under resting conditions. Transition in Homer isoforms compositon was studied under experimental conditions of short-term and long-term adaptation, e.g., fatigue and regeneration, respectively. First, we show that Homer 1a was constitutively expressed and was transiently upregulated during regeneration. In C2C12 cell cultures, Homer 1a was also upregulated during formation of myotubes. No change of Homer 1a was observed in fatigue. Second, Homer 1b/c/d and Homer 2b were positively and linearly related to muscle mass change during regeneration, and third, Homer 3 was not detectable under resting conditions but was transiently expressed during regeneration although with a temporal pattern distinct from that of Homer 1a. Thus a switch in Homer isoforms is associated to muscle differentiation and regeneration. Homers may play a role not only in signal transduction of skeletal muscle, in particular regulation of Ca2+ release from sarcoplasmic reticulum (Ward CW, Feng W, Tu J, Pessah IN, Worley PF, and Schneider MF. Homer protein increases activation of Ca2+ sparks in permeabilized skeletal muscle. J Biol Chem 279: 5781–5787, 2004), but also in adaptation.

fatigue; immediate early gene; muscle adaptation; myogenesis



Address for reprint requests and other correspondence: P. Volpe, Dipartimento di Scienze Biomediche Sperimentali, Università degli Studi di Padova, viale G. Colombo 3, 35121 Padova, Italy (e-mail: pompeo.volpe{at}unipd.it)







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