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Sequence characterization of the melanocortin 1 receptor (MC1R) gene in sheep with different coat colours and identification of the putative e allele at the ovine Extension locus

机译:不同皮毛颜色的绵羊中黑皮质素1受体(MC1R)基因的序列表征以及在绵羊延伸位点的推定e等位基因的鉴定

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摘要

Sequence of the melanocortin 1 receptor (MC1R) gene (the Extension locus) was obtained from a panel of 73 animals belonging to 9 Italian sheep breeds or populations (Appenninica, Bergamasca, Comisana, Cornigliese-like, Delle Langhe, Massese, Merinizzata Italiana, Sarda and Valle del Belice) with different coat colours. Evaluation of the identified polymorphisms on this phenotype was reported with in silico predictions and comparative approaches within and across breeds and across species. Five novel single nucleotide polymorphisms (SNPs), organized in three haplotypes, were detected. Another haplotype, including the two missense mutations already described for the E-D allele, was identified in few Massese sheep. One SNP (c.199C>T) caused a predicted amino acid substitution (p.R67C) in a highly conserved position of the first intracellular loop of the MC1R protein. The same substitution causes recessive pheomelanism in other species. We propose that the p.67C allele represents the recessive e allele at the ovine Extension series that was, so far, not completely recognized in sheep by classical genetic studies. This polymorphism was analysed in a total of 388 sheep of the 9 investigated breeds. The p.67C allele was identified only in the Valle del Belice breed (allele frequency of 21.3% in 176 analysed animals of this breed) in which the presence of epistatic white-determining loci might mask, at least in part, its effects. Confirming the effect of this novel allele on coat colour will lead to new perspectives on the composition of specialized coloured sheep lines.
机译:黑色皮质素1受体(MC1R)基因的序列(扩展基因座)是从属于9个意大利绵羊品种或种群的73种动物(阿彭尼尼卡,贝加马斯卡,科米萨纳,Corrigliese-like,戴尔·朗格,马塞斯,梅里尼扎塔·意大利, Sarda和Valle del Belice)具有不同的外套颜色。通过计算机模拟预测和在品种内和品种间以及物种间的比较方法,报告了对该表型鉴定出的多态性的评估。检测到五个新颖的单核苷酸多态性(SNP),以三种单倍型组织。在少数马塞羊中鉴定出另一种单倍型,包括已经针对E-D等位基因描述的两个错义突变。一个SNP(c.199C> T)在MC1R蛋白的第一个细胞内环的高度保守位置引起了预期的氨基酸取代(p.R67C)。相同的替代会在其他物种中引起隐性轻狂。我们建议p.67C等位基因代表绵羊延伸系列中的隐性e等位基因,到目前为止,经典遗传学研究尚未在绵羊中完全识别出该基因。在研究的9个品种的388只绵羊中分析了这种多态性。仅在Valle del Belice品种中鉴定出p.67C等位基因(在该品种的176只经分析的动物中,等位基因频率为21.3%),其中上位性白色决定基因座的存在可能至少部分掩盖了其作用。证实这种新颖的等位基因对大衣颜色的影响将导致对专门的彩色绵羊品系组成的新见解。

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