Blatter M, Haase B, Gerber V, Poncet P-A, Leeb T, Rieder S, Henke D, Janett F, Burger D
Institut Suisse de Médicine Equine, ALP-Haras und Universität Bern.
Schweiz Arch Tierheilkd. 2013 Apr;155(4):229-32. doi: 10.1024/0036-7281/a000451.
In April 2008 a Franches-Montagnes colt was born with an unusual coat colour phenotype which had never been observed in that population before. The foal showed extended white markings on body and legs, a white head and blue eyes. As both parents have an unremarkable bay coat colour phenotype, a de novo mutation was expected in the offspring and a candidate gene approach revealed a spontaneous mutation in the microphthalmia associated transcription factor gene (MITF). A detailed clinical examination in 2010 indicated an impaired hearing capacity. As in the American Paint Horse large white facial markings in combination with blue eyes are associated with deafness, the hearing capacity of the stallion was closer examined performing brainstem auditory-evoked responses (BAER). The BAER confirmed bilateral deafness in the Franches-Montagnes colt. It is assumed that the deafness is caused by a melanocyte deficiency caused by the MITF gene mutation. Unfortunately, due to castration of the horse, the causal association between the mutation in the MITF gene and clinical findings cannot be confirmed by experimental matings.
2008年4月,一匹弗朗什-蒙塔涅马驹出生,其毛色表型异常,在该种群中此前从未见过。这匹小马驹身体和腿部有大面积白色斑纹,头部白色,眼睛蓝色。由于双亲的毛色表型均为普通的枣色,预计后代发生了新生突变,通过候选基因方法发现小眼畸形相关转录因子基因(MITF)存在自发突变。2010年的详细临床检查表明其听力受损。由于在美国花马中,大面积白色面部斑纹与蓝色眼睛相结合与耳聋有关,因此对这匹种马的听力进行了更仔细的检查,采用脑干听觉诱发电位(BAER)检测。BAER证实这匹弗朗什-蒙塔涅马驹双耳失聪。据推测,耳聋是由MITF基因突变导致的黑素细胞缺乏引起的。不幸的是,由于这匹马已被阉割,无法通过实验性配种来证实MITF基因突变与临床症状之间的因果关系。