Abstract
Fifty-four primer pairs were designed for expressed sequence tag (EST) sequences containing perfect di- and tri-nucleotide motifs and characterised in 96 unrelated fish. Twenty markers were successfully amplified with number of alleles from 2 to 10 per locus and observed and expected heterozygosity ranging from 0.01 to 0.56 and 0.03 to 0.70, respectively. Loci Gmo-C213, Gmo-C246 and Gmo-C247 deviated from Hardy–Weinberg equilibrium. Genetic linkage disequilibrium analysis between all pairs of the loci showed significant departure from the null hypothesis between loci Gmo-C213 and Gmo-C222, Gmo-C233 and Gmo-C229, C223 and Gmo-C236 and C229 and Gmo-C236. The gene identity was determined at 10 of the loci, confirming the associated microsatellites as Type I markers. These microsatellite markers provide useful tools for studies of population genetics, reproductive ecology and constructing linkage maps of Atlantic cod.
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Acknowledgements
The present study was supported by the National Programme for Research in Functional Genomics in Norway (FUGE) within the Research Council of Norway (GenoFish). We thank Dr. Marie Cooper for reading of the manuscript and making helpful suggestions.
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Delghandi, M., Wesmajervi, M.S., Mennen, S. et al. Development of twenty sequence-tagged microsatellites for the Atlantic cod (Gadus morhua L.). Conserv Genet 9, 1395–1398 (2008). https://doi.org/10.1007/s10592-008-9507-3
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DOI: https://doi.org/10.1007/s10592-008-9507-3