Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies)

• Autor(a) principal: Anderson, Louise V.B.
• Data de Publicação: 2000
• Outros Autores: Harrison, Ruth M., Pogue, Robert, Vafiadaki, Elizabeth, Pollitt, Christine, Davison, Keith, Moss, Jennifer A., Keers, Sharon, Pyle, Ângela, Shaw, Pamela J., Mahjneh, Ibrahim, Argov, Zohar, Greenberg, Cheryl R., Wrogemann, Klaus, Bertorini, Túlio, Goebel, Hans H., Beckmann, Jacques S., Bashir, Rumaisa, Bushby, Kate M.D.
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Institucional da UCB
• Texto Completo: http://twingo.ucb.br:8080/jspui/handle/10869/474; https://repositorio.ucb.br:9443/jspui/handle/123456789/7671
• topic: Dysferlin; Calpain 3; Laminin; Merosin; Muscular dystrophy; Muscle proteins; Western blotting

Dysferlin is the protein product of the gene (DYSF) that is defective in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy. Calpain 3 is the muscle-speci®c member of the calcium activated neutral protease family and primary mutations in the CAPN3 gene cause limb girdle muscular dystrophy type 2A. The functions of both proteins remain speculative. Here we report a secondary reduction in calpain 3 expression in eight out of 16 patients with a primary dysferlinopathy and clinical features characteristic of limb girdle muscular dystrophy type 2B or Miyoshi myopathy. Previously CAPN3 analysis had been undertaken in three of these patients and two showed seemingly innocuous missense mutations, changing calpain 3 amino acids to those present in the sequences of calpains 1 and 2. These results suggest that there may be an association between dysferlin and calpain 3, and further analysis of both genes may elucidate a novel functional interaction. In addition, an association was found between prominent expression of smaller forms of the 80 kDa fragment of laminin a2 chain (merosin) and dysferlin-de®ciency.