Faculty of Veterinary Medicine and Animal Science, Federal University of Mato Grosso do Sul, Campo Grande, Brazil.
J Vet Diagn Invest. 2021 Sep;33(5):984-986. doi: 10.1177/10406387211022309. Epub 2021 Jun 4.
Color dilution alopecia (CDA) is a dermatopathy observed exclusively in animals having a diluted coat color. In dogs, color dilution occurs as a result of a single-nucleotide variation (SNV) in the melanophilin gene. We standardized a PCR-restriction-fragment length polymorphism (PCR-RFLP) technique to identify this mutation and determine its frequency in dogs in Brazil. The standardized PCR-RFLP technique could efficiently identify the SNV in the melanophilin gene, with mutated allele frequencies of 0.1, 0.1, and 0.0875 in Dachshund, Miniature Pinscher, and Yorkshire Terrier breeds, respectively, with no statistical difference among the breeds ( = 0.252). The mutation was identified in 2 homozygous Dachshund dogs with alopecia, confirming the clinical characteristic of CDA. The standardization of a simpler and more accessible molecular technique for recognition of the SNV in the melanophilin gene allows identification of heterozygous (phenotypically normal) dogs that can be excluded from reproduction, to avoid the birth of dogs with diluted coat color and consequently CDA.
色素稀释性脱毛症(CDA)是一种仅在具有稀释毛色的动物中观察到的皮肤疾病。在犬中,毛色稀释是由于黑素磷蛋白基因中的单个核苷酸变异(SNV)引起的。我们标准化了一种聚合酶链反应-限制性片段长度多态性(PCR-RFLP)技术,以鉴定该突变并确定其在巴西犬中的频率。标准化的 PCR-RFLP 技术能够有效地鉴定黑素磷蛋白基因中的 SNV,突变等位基因频率分别为 0.1、0.1 和 0.0875,在达克斯猎犬、迷你雪纳瑞犬和约克夏梗犬品种中,品种间无统计学差异( = 0.252)。在 2 只患有脱毛症的纯合达克斯猎犬中鉴定出该突变,证实了 CDA 的临床特征。标准化一种更简单、更容易获得的分子技术来识别黑素磷蛋白基因中的 SNV,可以识别出杂合子(表型正常)的狗,并将其排除在繁殖之外,以避免稀释毛色和 CDA 的犬只出生。