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黑皮质素1受体的突变与挪威森林猫的琥珀色毛色有关。

Mutation in the melanocortin 1 receptor is associated with amber colour in the Norwegian Forest Cat.

作者信息

Peterschmitt M, Grain F, Arnaud B, Deléage G, Lambert V

机构信息

Université de Lyon, Ecole Nationale Vétérinaire de Lyon, Unité Génétique & Biologie Moléculaire et Laboratoire Vétérinaire Départemental du Rhône, F-69280 Marcy l'Etoile, France.

出版信息

Anim Genet. 2009 Aug;40(4):547-52. doi: 10.1111/j.1365-2052.2009.01864.x. Epub 2009 Apr 24.

DOI:10.1111/j.1365-2052.2009.01864.x
PMID:19422360
Abstract

Amber (previously called X-Colour) is a yellow recessive coat colour observed in the Norwegian Forest Cat (NFC) population and apparently absent in other cat breeds. Until now, there has never been any scientific evidence of yellow recessive mutation (e) reported in the extension gene in Felidae. We sequenced the complete coding sequence region for the melanocortin 1 receptor in 12 amber, three carriers, two wild-type NFCs, one wild-type European Shorthair and two 'golden' Siberian cats and identified two single nucleotide polymorphisms (SNPs): a non-synonymous (FM180571: c.250G>A) and a synonymous (FM180571: c.840T>C) mutation. The c.250G>A SNP, further genotyped on 56 cats using PCR-RFLP, is associated with amber colour and only present in the amber cat lineages. It replaced an aspartic acid with a neutral polar asparagine in the second transmembrane helix (p.Asp84Asn), a position where e mutations have already been described. Three-dimensional models were built and showed electrostatic potential modification in the mutant receptor. With these results and together with those in the scientific literature, we can conclude that amber colour in NFCs is caused by a single MC1R allele called e, which has never been documented.

摘要

琥珀色(以前称为X色)是挪威森林猫(NFC)种群中观察到的一种黄色隐性毛色,在其他猫品种中显然不存在。到目前为止,在猫科动物的扩展基因中从未有过黄色隐性突变(e)的科学证据报道。我们对12只琥珀色猫、3只携带者、2只野生型NFC、1只野生型欧洲短毛猫和2只“金色”西伯利亚猫的黑皮质素1受体完整编码序列区域进行了测序,鉴定出两个单核苷酸多态性(SNP):一个非同义突变(FM180571:c.250G>A)和一个同义突变(FM180571:c.840T>C)。使用PCR-RFLP在56只猫上进一步对c.250G>A SNP进行基因分型,发现其与琥珀色相关,且仅存在于琥珀色猫系中。它在第二个跨膜螺旋中将天冬氨酸替换为中性极性天冬酰胺(p.Asp84Asn),该位置已经描述过e突变。构建了三维模型,显示突变受体的静电势发生了改变。基于这些结果以及科学文献中的结果,我们可以得出结论,NFC中的琥珀色是由一个名为e的单一MC1R等位基因引起的,这从未有过记录。

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