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破坏肌肉生长抑制素功能并导致牛双肌现象的一系列等位基因突变的分子定义。

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

作者信息

Grobet L, Poncelet D, Royo L J, Brouwers B, Pirottin D, Michaux C, Ménissier F, Zanotti M, Dunner S, Georges M

机构信息

Department of Genetics, Faculty of Veterinary Medicine, University of Liège (B43), Belgium.

出版信息

Mamm Genome. 1998 Mar;9(3):210-3. doi: 10.1007/s003359900727.

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.

摘要

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。

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