Genetische Analyse der kongenitalen Hypotrichose mit Anodontie beim Rind

Abstract. Title of the paper: Genetic analysis of congenital hypotrichosis with anodontia in cattle
In three male German Holstein calves, black and white spotted, congenital hypotrichosis and nearly complete anodontia was observed. The pedigree of the probands being maternal halfsibs and grandmatemal grandsons supports a monogenic, X-linked recessive inheritance. Chromosomal Xq-deletions were not detected. Similar congenital anomalies are known in tabby mice and in humans as anhidrotic ectodermal dysplasia (EDI, EDA). The human gene causative for EDI and the Tabby gene are located on the X-chromosome. Therefore, the moleculargenetic marker analysis in our material was restricted on the X-chromosome. Using identical by descend mapping based on 20 microsatellites, we were able to identify an exclusively Joint genomic region on the long arm of the X-chromosome among the affected calves. The putative location of the gene locus for congenital hypotrichosis with anodontia maps into the region of the marker BM4604 on position 76.5 cM of the X-chromosome.