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Molecular definition of an allelic series of mutations disrupting the myostatin function and causing double-muscling in cattle.
Grobet, L; Poncelet, D; Royo, L J; Brouwers, B; Pirottin, D; Michaux, C; Ménissier, F; Zanotti, M; Dunner, S; Georges, M.
Afiliação
  • Grobet L; Department of Genetics, Faculty of Veterinary Medicine, University of Liège (B43), Belgium.
Mamm Genome ; 9(3): 210-3, 1998 Mar.
Article em En | MEDLINE | ID: mdl-9501304
ABSTRACT
We have determined the entire myostatin coding sequence for 32 double-muscled cattle sampled from ten European cattle breeds. Seven DNA sequence polymorphisms were identified, of which five would be predicted to disrupt the function of the protein, one is a conservative amino acid substitution, and one a silent DNA sequence variant. Four additional DNA sequence polymorphisms were identified in myostatin intronic sequences. In all but two breeds, all double-muscled animals were either homozygous or compound heterozygotes for one of the five loss-of-function mutations. The absence of obvious loss-of-function mutations in the coding sequence of the two remaining breeds points either towards additional mutations in unexplored segments of the gene, or towards locus heterogeneity of double-muscling.
Assuntos
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Base de dados: MEDLINE Assunto principal: Fator de Crescimento Transformador beta / Doenças Musculoesqueléticas / Músculo Esquelético / Alelos / Mutação Idioma: En Ano de publicação: 1998 Tipo de documento: Article
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Base de dados: MEDLINE Assunto principal: Fator de Crescimento Transformador beta / Doenças Musculoesqueléticas / Músculo Esquelético / Alelos / Mutação Idioma: En Ano de publicação: 1998 Tipo de documento: Article