A mutation creating a potential illegitimate microRNA target site in the myostatin gene affects muscularity in sheep

被引:1089
作者
Clop, Alex
Marcq, Fabienne
Takeda, Haruko
Pirottin, Dimitri
Tordoir, Xavier
Bibe, Bernard
Bouix, Jacques
Caiment, Florian
Elsen, Jean-Michel
Eychenne, Francis
Larzul, Catherine
Laville, Elisabeth
Meish, Francoise
Milenkovic, Dragan
Tobin, James
Charlier, Carole
Georges, Michel
机构
[1] Univ Liege, Fac Vet Med, Dept Anim Prod, Unit Anim Genom, B-4000 Liege, Belgium
[2] Univ Liege, Ctr Biomed Integrat Genoprote, B-4000 Liege, Belgium
[3] INRA, SAGA, Stn Ameliorat Genet Anim, F-31326 Castanet Tolosan, France
[4] INRA, Rech Viande Stn, F-63122 St Genes Champanelle, France
[5] Univ Limoges, Fac Sci, INRA, F-87060 Limoges, France
[6] Wyeth Ayerst Res, Cardiovasc & Metab Dis, Cambridge, MA 02140 USA
关键词
D O I
10.1038/ng1810
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学]; 090102 [作物遗传育种];
摘要
Texel sheep are renowned for their exceptional meatiness. To identify the genes underlying this economically important feature, we performed a whole-genome scan in a Romanov x Texel F2 population. We mapped a quantitative trait locus with a major effect on muscle mass to chromosome 2 and subsequently fine-mapped it to a chromosome interval encompassing the myostatin (GDF8) gene. We herein demonstrate that the GDF8 allele of Texel sheep is characterized by a G to A transition in the 3' UTR that creates a target site for mir1 and mir206, microRNAs (miRNAs) that are highly expressed in skeletal muscle. This causes translational inhibition of the myostatin gene and hence contributes to the muscular hypertrophy of Texel sheep. Analysis of SNP databases for humans and mice demonstrates that mutations creating or destroying putative miRNA target sites are abundant and might be important effectors of phenotypic variation.
引用
收藏
页码:813 / 818
页数:6
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