Grobet L, Poncelet D, Royo L J, Brouwers B, Pirottin D, Michaux C, Ménissier F, Zanotti M, Dunner S, Georges M
Department of Genetics, Faculty of Veterinary Medicine, University of Liège (B43), Belgium.
Mamm Genome. 1998 Mar;9(3):210-3. doi: 10.1007/s003359900727.
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.
我们已经确定了从十个欧洲牛品种中采样的32头双肌牛的整个肌肉生长抑制素编码序列。鉴定出七个DNA序列多态性,其中五个预计会破坏蛋白质的功能,一个是保守的氨基酸取代,一个是沉默的DNA序列变体。在肌肉生长抑制素内含子序列中又鉴定出四个DNA序列多态性。除两个品种外,在所有品种中,所有双肌动物对于五个功能丧失突变之一均为纯合子或复合杂合子。其余两个品种的编码序列中没有明显的功能丧失突变,这要么表明该基因未探索区段存在额外突变,要么表明双肌现象存在基因座异质性。