Molecular definition of an allelic series of mutations disrupting the myostatin function and causing double-muscling in cattle

被引:449
|
作者
Grobet, L
Poncelet, D
Royo, LJ
Brouwers, B
Pirottin, D
Michaux, C
Ménissier, F
Zanotti, M
Dunner, S
Georges, M
机构
[1] Univ Liege, Dept Genet, Fac Vet Med, B-4000 Liege, Belgium
[2] Univ Complutense, Genet Lab, Dpto Producc Anim, E-28040 Madrid, Spain
[3] INRA, Genet Quantitat & Appl Stn, F-78352 Jouy En Josas, France
[4] Univ Milan, Fac Med Vet, Ist Zool, I-20133 Milan, Italy
关键词
D O I
10.1007/s003359900727
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 poly morphisms 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 rewards locus heterogeneity of double-muscling.
引用
收藏
页码:210 / 213
页数:4
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