Genetic variations and dog breed identification using inter-simple sequence repeat markers coupled with high resolution melting analysis

Author:

Kriangwanich Wannapimol1,Nganvongpanit Korakot12,Buddhachat Kittisak23,Siengdee Puntita24,Chomdej Siriwadee25,Ponsuksili Siriluck4,Thitaram Chatchote6

Affiliation:

1. Department of Veterinary Biosciences and Public Health, Faculty of Veterinary Medicine, Chiang Mai University, Chiang Mai, Thailand

2. Excellence Center in Veterinary Bioscience, Chiang Mai University, Chiang Mai, Thailand

3. Department of Biology, Faculty of Science, Naresuan University, Phitsanulok, Thailand

4. Leibniz Institute for Farm Animal Biology, Dummerstorf, Germany

5. Department of Biology, Faculty of Science, Chiang Mai University, Chiang Mai, Thailand

6. Center of Excellence in Elephant and Wildlife Research, Faculty of Veterinary Medicine, Chiang Mai University, Chiang Mai, Thailand

Abstract

The identification of differing physical characteristics of dogs is an uncomplicated and straightforward way to categorize dog breeds. However, many dog owners and veterinarians still struggle to distinguish between pure breed and mixed variations in certain breeds of dogs. Presently, the absence of the tools and methods needed to confirm a pure breed dog is a significant problem since the only method available to validate pure or mongrel breeds is the official pedigree system. Inter-simple sequence repeat markers have been successfully used to assess genetic variations and differentiations. Notably, inter-simple sequence repeat markers coupled with high resolution melting analysis were effectively used for the breed identification of 43 breeds of dogs (total 463 dogs). The 10 primers chosen for analysis resulted in a range of 31–78.6% of breed discrimination when using one primer, while a combination of two primers was able to successfully discriminate between all of the 43 dog breeds (100%). Shannon’s index information (I = 2.586 ± 0.034) and expected heterozygosity (He = 0.908 ± 0.003) indicated a high level of genetic diversity among breeds. The fixation index (Fst) revealed a value of 10.4%, demonstrating that there was a high level of genetic subdivision between populations. This study showed that inter-simple sequence repeat marker analysis was effective in demonstrating high genetic diversity among varying breeds of dogs, while a combination of Inter-simple sequence repeat marker analysis and high resolution melting analysis could provide an optional technique for researchers to effectively identify breeds through genetic variations.

Funder

The Royal Jubilee Ph.D. Program, Thailand Research Fund

Faculty of Veterinary Medicine, Chiang Mai University, Thailand

Excellence Center in Veterinary Bioscience (ECVB), Chiang Mai University, Thailand

Publisher

PeerJ

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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