Elsevier

Aquaculture

Volume 137, Issues 1–4, 1 December 1995, Pages 19-30
Aquaculture

Isolation of salmonid microsatellite loci and their application to the population genetics of Canadian east coast stocks of Atlantic salmon

https://doi.org/10.1016/0044-8486(95)01111-0Get rights and content

Abstract

Genetic variation at four microsatellite loci, two isolated from Atlantic salmon and two from rainbow trout, was assayed in five populations of Alantic salmon from Nova Scotia, Canada and in samples from Norway and Ireland. Up to 38 allelles per locus and heterozygosities of 0.9 were observed at some loci. Genetic distances, calculated over the four loci for all population samples show a clear grouping of populations according to geographic location. These loci show potential as genetic markers in Atlantic salmon due to the range of polymorphisms observed among individual loci and to the ease and speed of sample assay. Highly variable loci will be of use in the ‘genetic tagging’ of cultured fish and in the assessment of levels of gene introgression from cultured to wild stocks. The clear differences in both allele frequencies and alleles observed between continents will be of value in the assessment of the relative sizes of the contributions of Canadian and North European salmon to the mixed fishery off Greenland.

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      Genomic DNA for microsatellite analysis was extracted from adipose fin tissue using the HotSHOT protocol (Truett et al., 2000). A panel of 19 microsatellite loci, in five PCR multiplexes, was used to characterise each fish (Table A.1); this comprised two expressed sequence tag-related loci (ESTs) CAO48828, CAO6177 (Vasemagi et al., 2005), an MHC-linked microsatellite (Sasa-TAP2A; Grimholt et al., 2002) and 16 neutral microsatellite markers (Ikediashi et al., 2012): Ssosl417, Ssosl85 (Slettan et al., 1995), Ssa202, Ssa197, Ssa171 (O'Reilly et al., 1996), SSspG7, SSsp3016, SSsp2216, SSsp2210, SSsp1605, SSsp2201 (Paterson et al., 2004), Ssa14, Ssa289 (McConnell et al., 1995), SsaF43 (Sanchez et al., 1996), SsaD144, SsaD157 (King et al., 2005). Polymerase chain reaction (PCR) amplification was performed in a 10 μl reaction mixture consisting of 1 μl DNA (approximately 10–30 ng), 1 μl primer mix, 3 μl water and 5 μl 2 × Mastermix from a Qiagen HotStarTaq mastermix kit.

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    1

    Present adress: School of Fisheries, University of Washington, Seattle WA. 98195 USA.

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