Association between MC1R gene and coat color segregation in Shanxia long black pig and Lulai black pig.

IF 1.9 Q3 GENETICS & HEREDITY
Hao Zheng, San-Ya Xiong, Shi-Jun Xiao, Ze-Kai Zhang, Jin-Min Tu, Deng-Shuai Cui, Nai-Biao Yu, Zhi-Yong Huang, Long-Yun Li, Yuan-Mei Guo
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引用次数: 0

Abstract

Background: Coat color, as a distinct phenotypic characteristic of pigs, is often subject to preference and selection, such as in the breeding process of new breed. Shanxia long black pig was derived from an intercross between Berkshire boars and Licha black pig sows, and it was bred as a paternal strain with high-quality meat and black coat color. Although the coat color was black in the F1 generation of the intercross, it segregated in the subsequent generations. This study aims to decode the genetic basis of coat color segregation and develop a method to distinct black pigs from the spotted in Shanxia long black pig.

Results: Only a QTL was mapped at the proximal end of chromosome 6, and MC1R gene was picked out as functional candidate gene. A total of 11 polymorphic loci were identified in MC1R gene, and only the c.67_68insCC variant was co-segregating with coat color. This locus isn't recognized by any restriction endonuclease, so it can't be genotyped by PCR-RFLP. The c.370G > A polymorphic locus was also significantly associated with coat color, and has been in tightly linkage disequilibrium with the c.67_68insCC. Furthermore, it is recognized by BspHI. Therefore, a PCR-RFLP method was set up to genotype this locus. Besides the 175 sequenced individuals, another more 1,391 pigs were genotyped with PCR-RFLP, and all of pigs with GG (one band) were black.

Conclusion: MC1R gene (c.67_68insCC) is the causative gene (mutation) for the coat color segregation, and the PCR-RFLP of c.370G > A could be used in the breeding program of Shanxia long black pig.

MC1R基因与山西长黑猪和鲁来黑猪被毛色差的关系
背景:毛色作为猪的一种明显的表型特征,经常受到偏好和选择的影响,例如在新品种的育种过程中。山西长黑猪是由波克夏公猪和李察黑猪杂交而成,是一种肉质优良、毛色黑色的父系品种。杂交的F1代虽然被毛为黑色,但在后代中发生了分离。本研究旨在对陕西长黑猪毛色分离的遗传基础进行解码,并建立一种区分黑猪和斑点猪的方法。结果:仅在6号染色体近端定位到一个QTL,筛选出MC1R基因作为功能性候选基因。MC1R基因共鉴定出11个多态性位点,只有c.67_68insCC变异位点与毛色共分离。该位点不被任何限制性内切酶识别,因此无法通过PCR-RFLP进行基因分型。c.370G > A多态性位点也与被毛颜色显著相关,且与c.67_68insCC存在紧密的连锁不平衡。此外,它被BspHI识别。因此,建立了PCR-RFLP方法对该位点进行基因分型。除175头猪外,还有1391头猪进行了PCR-RFLP基因分型,所有GG(1条带)猪均为黑色。结论:MC1R基因(c.67_68insCC)是引起毛色分离的致病基因(突变基因),c.370G > A的PCR-RFLP可用于山西长黑猪的育种规划。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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