Abstract

Arbitrary primer polymerase chain reaction (AP-PCR) detected anonymous DNA polymorphisms between individual representatives of seven breeds of dogs, between members of a single breed, and between members of a single family of dogs. Short arbitrary sequence PCR primers and promoter/protein motif sequence primers typically amplified 15–30 bands ranging from 200–2000 bp in length. The average heterozygosity of 10 line bred Belgian sheepdogs (H = 0.024 ± 0.011, mean ± 95% Cl) was significantly lower than that of a panel of unrelated beagles (H = 0.057 ± 0.018, mean ± 95% Cl, P <.01). The average heterozygosity of a seven-breed panel was intermediate between the two (H = 0.043 ± 0.011, mean ± 95% Cl) and not significantly different than either panel. One motif sequence PCR primer pair yielded products that strongly differentiated between Belgian sheepdogs, beagles, and members of five other breeds. AP-PCR could be used to generate DNA fingerprints that distinguish between dog breeds, as well as to provide markers in this sparsely mapped genome.

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