Abstract
Genetic analysis has shown to be an important and efficient method for monitoring species, but the lack of genetic markers constrains such monitoring for many species. Here, we cross-amplified microsatellite loci in the snowy owl (Bubo scandiacus) using primers previously characterized in other species. Among polymorphic loci, we selected 12 loci that amplified relatively short fragments (<250 base pairs) to facilitate genotyping of moulted feathers and other non-invasively collected samples. These 12 loci, and a sex-typing marker, were amplified in two multiplex PCR sets and used to screen 49 snowy owls from a northern European population. The number of alleles observed at single loci was 2 to 17. Expected and observed heterozygosity ranged from 0.12 to 0.91 and from 0.12 to 0.96, respectively. The combined probability of identity for the 12 loci was 5.7 × 10−11. Our multiplex PCR assays are expected to be useful for genetic monitoring, parentage analysis, and population genetic studies of the snowy owl.
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