Construction of an individual identification panel for horses using insertion and deletion markers

• Published in: Journal of Equine Science Vol. 34; no. 3; pp. 83 - 92
• Main Authors: TOZAKI, Teruaki, OHNUMA, Aoi, KIKUCHI, Mio, ISHIGE, Taichiro, KAKOI, Hironaga, HIROTA, Kei-ichi, NAGATA, Shun-ichi
• Format: Journal Article
• Language: English
• Published: Utsunomiya-shi Japanese Society of Equine Science 2023; Japan Science and Technology Agency; The Japanese Society of Equine Science
• Subjects: Deletion; Domestic animals; Gene frequency; Genotyping; Horse racing; Horses; Inbreeding; Insertion; insertion/deletion; Mutation rates; Nucleotides; parentage testing; Paternity; Paternity testing; Racehorses; Short tandem repeats; single nucleotide variant; Thoroughbred
• ISSN: 1340-3516; 1347-7501
• DOI: 10.1294/jes.34.83

Individual identification and paternity testing are important for avoiding inbreeding in the management of small populations of wild and domestic animals. In horse racing industries, they are extremely important for identifying and registering individuals and doping control to ensure fair competition. In this study, we constructed an individual identification panel for horses by using insertion and deletion (INDEL) markers. The panel included 39 INDEL markers selected from a whole-genome INDEL database. Genotyping of 89 Thoroughbreds showed polymorphisms with minor allele frequencies (MAFs) of 0.180–0.489 in all markers. The total probability of exclusion for paternity testing, power of discrimination, and probability of identity were 0.9994271269, >0.9999999999, and 0.9999999987, respectively. The panel was applied to 13 trios (sires, dams, and foals), and no contradictions were observed in genetic inheritance among the trios. When this panel was applied to the trios (52 trios) containing false fathers, an average of 7.3 markers excluded parentage relationships. In addition, genomic DNA extracted from the urine of six horses was partially genotyped for 39 markers, and 6–28 markers were successfully genotyped. The newly constructed panel has two advantages: a low marker mutation rate compared with short tandem repeats and a genotyping procedure that is as simple as short tandem repeat typing compared with single nucleotide variant typing. This panel can be applied for individual identification, paternity determination, and urine-sample identification in Thoroughbred horses.