Brunberg Emma, Andersson Leif, Cothran Gus, Sandberg Kaj, Mikko Sofia, Lindgren Gabriella
Dept of Medical Biochemistry and Microbiology, Uppsala University, SE-751 24 Uppsala, Sweden.
BMC Genet. 2006 Oct 9;7:46. doi: 10.1186/1471-2156-7-46.
The Silver coat color, also called Silver dapple, in the horse is characterized by dilution of the black pigment in the hair. This phenotype shows an autosomal dominant inheritance. The effect of the mutation is most visible in the long hairs of the mane and tail, which are diluted to a mixture of white and gray hairs. Herein we describe the identification of the responsible gene and a missense mutation associated with the Silver phenotype.
Segregation data on the Silver locus (Z) were obtained within one half-sib family that consisted of a heterozygous Silver colored stallion with 34 offspring and their 29 non-Silver dams. We typed 41 genetic markers well spread over the horse genome, including one single microsatellite marker (TKY284) close to the candidate gene PMEL17 on horse chromosome 6 (ECA6q23). Significant linkage was found between the Silver phenotype and TKY284 (theta = 0, z = 9.0). DNA sequencing of PMEL17 in Silver and non-Silver horses revealed a missense mutation in exon 11 changing the second amino acid in the cytoplasmic region from arginine to cysteine (Arg618Cys). This mutation showed complete association with the Silver phenotype across multiple horse breeds, and was not found among non-Silver horses with one clear exception; a chestnut colored individual that had several Silver offspring when mated to different non-Silver stallions also carried the exon 11 mutation. In total, 64 Silver horses from six breeds and 85 non-Silver horses from 14 breeds were tested for the exon 11 mutation. One additional mutation located in intron 9, only 759 bases from the missense mutation, also showed complete association with the Silver phenotype. However, as one could expect to find several non-causative mutations completely associated with the Silver mutation, we argue that the missense mutation is more likely to be causative.
The present study shows that PMEL17 causes the Silver coat color in the horse and enable genetic testing for this trait.
马的银色被毛颜色,也称为银斑色,其特征是毛发中的黑色色素被稀释。这种表型呈常染色体显性遗传。该突变的影响在鬃毛和尾巴的长毛中最为明显,这些毛发被稀释成白色和灰色毛发的混合物。在此,我们描述了相关基因的鉴定以及与银色表型相关的错义突变。
在一个半同胞家系中获得了银色基因座(Z)的分离数据,该家系由一匹杂合银色种马及其34个后代和29匹非银色母马组成。我们对分布在马基因组中的41个遗传标记进行了分型,包括一个位于马6号染色体(ECA6q23)上靠近候选基因PMEL17的单微卫星标记(TKY284)。在银色表型与TKY284之间发现了显著的连锁关系(θ = 0,z = 9.0)。对银色和非银色马的PMEL17进行DNA测序,发现在外显子11中有一个错义突变,该突变使细胞质区域的第二个氨基酸从精氨酸变为半胱氨酸(Arg618Cys)。这种突变在多个马品种中与银色表型完全相关,在非银色马中未发现,但有一个明显的例外;一匹栗色个体在与不同的非银色种马交配时产下了几匹银色后代,它也携带外显子11突变。总共对来自6个品种的64匹银色马和来自14个品种的85匹非银色马进行了外显子11突变检测。位于内含子9中的另一个突变,距离错义突变仅759个碱基,也与银色表型完全相关。然而,正如人们可能预期会发现一些与银色突变完全相关的非致病变异一样,我们认为错义突变更有可能是致病的。
本研究表明PMEL17导致马的银色被毛颜色,并能够对该性状进行基因检测。