与不同马种脱色有关的三种 HPS5 基因突变

IF 1.8 3区 农林科学 Q2 AGRICULTURE, DAIRY & ANIMAL SCIENCE
Aiden McFadden , Katie Martin , Micaela Vierra , Holly Robilliard , Erica W. Lundquist , Robin E. Everts , Samantha A. Brooks , Christa Lafayette
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引用次数: 0

摘要

脱色是马的一种常见表型;超过 50 种已确定的变体会导致皮肤和皮毛上出现白斑。在此,我们报告了在大多数主要马种中发现的三种与白斑病有关的马基因突变。我们采用标准化方法对脱色进行量化分级,为每匹马制定了一个白斑评分。我们将携带者的平均白分与 41 匹未携带任何变异的对照马的平均白分进行了比较,从而确定了三种变异中每一种变异的相关性。我们利用 SIFT、GenScan、I-TASSER 和跨物种保护来估计每个变异的功能影响。第一个变异 S1013C 被称为Ⅳ,是一个错义突变,平均色素沉着增加了 5.56 个点(=6.47E-6,n=70,-test)。外显子 4+4 的一个假定供体剪接位点突变使白色平均增加了 5.59 点(=9.56E-6,n=101)。拥有显性等位基因的个体会产生黑色素,与隐性栗色基因型()的个体相比,该等位基因与较高的脱色水平相关(分别为=1.50E-5、=1.26E-5)。我们检测了 和 之间的外显相互作用,发现每个等位基因都有一个拷贝的马匹的平均白斑比或 的马匹增加了 8 个点。复合杂合子的白斑明显多于任何一个突变拷贝的马(=7.33E-5),但其他白斑等位基因与 EDXW 等位基因之间的相互作用仍有待检测。我们建议用()来表示家马的突变。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Three HPS5 mutations associated with depigmentation in diverse horse breeds

Depigmentation is a common phenotype in Equus caballus (horse); over 50 identified variants cause white spotting on the skin and coat. HPS5 may influence melanocyte proliferation and mutations in this gene cause depigmentation in humans, mice, and zebrafish. Here we report three equine HPS5 mutations, found in most major breed groups and associated with white spotting. We used a standardized method to quantitatively grade depigmentation, creating a White Score for each horse. We identified associations to each of three variants in HPS5 by comparing the average white score for carriers to that of 41 control horses possessing none of the studied variants. We estimated the functional impact of each mutation using SIFT, GenScan, I-TASSER and cross-species conservation. The first mutation, S1013C termed Eden White 1 (EDXW1), is a missense mutation found to increase average depigmentation by 5.56 points (p = 6.47E-6, n = 70, t-test). Eden White 2 (EDXW2), a missense mutation L560F, increased depigmentation by 9.5 points for individuals with one copy of the variant, but we were unable to phenotype homozygotes (p = 5.55E-16, n = 47, t-test). Eden White 3 (EDXW3), a putative donor splice site mutation at exon 4 + 4, increased white by 5.59 points on average (p = 9.56E-6, n = 101). EDXW1 and EDXW3 are epistatically influenced by MC1R, the gene that controls black vs red coat color in horses. Individuals possessing the dominant E allele produce black pigment, and this allele was associated with higher levels of depigmentation than individuals with the recessive chestnut genotype (e/e) (p = 1.50E-5, p = 1.26E-5 respectively). We tested for epistatic interactions between EDXW1 and Dominant White 20 and found that horses with one copy of each allele had increased average white spotting by 8 points with respect to EDXW1/n or W20/n horses. Compound heterozygotes were significantly more white than horses with one copy of either mutation (p = 7.33E-5), but interactions between other white spotting alleles and EDXW alleles remain to be tested. We propose the convention Eden White (EDXW) for HPS5 mutations in the domestic horse.

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来源期刊
Livestock Science
Livestock Science 农林科学-奶制品与动物科学
CiteScore
4.30
自引率
5.60%
发文量
237
审稿时长
3 months
期刊介绍: Livestock Science promotes the sound development of the livestock sector by publishing original, peer-reviewed research and review articles covering all aspects of this broad field. The journal welcomes submissions on the avant-garde areas of animal genetics, breeding, growth, reproduction, nutrition, physiology, and behaviour in addition to genetic resources, welfare, ethics, health, management and production systems. The high-quality content of this journal reflects the truly international nature of this broad area of research.
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