Estimation of population structure in coastal Douglas-fir [Pseudotsuga menziesii (Mirb.) Franco var. menziesii] using allozyme and microsatellite markers

• Published in: Tree genetics & genomes Vol. 5; no. 4; pp. 641 - 658
• Main Authors: Krutovsky, Konstantin V, St. Clair, John Bradley, Saich, Robert, Hipkins, Valerie D, Neale, David B
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Berlin/Heidelberg : Springer-Verlag 01-10-2009; Springer-Verlag; Springer Nature B.V
• Subjects: Animal populations; Biomedical and Life Sciences; Biotechnology; Forestry; Genetic diversity; Genotypes; Life Sciences; Original Paper; Plant Breeding/Biotechnology; Plant Genetics and Genomics; Population structure; Pseudotsuga menziesii; Simulation analysis; Tree Biology; Genetic markers; Microsatellites; SSR; var; Population structure; Allozyme; Simple sequence repeats
• ISSN: 1614-2942; 1614-2950
• DOI: 10.1007/s11295-009-0216-y

Characterizing population structure using neutral markers is an important first step in association genetic studies in order to avoid false associations between phenotypes and genotypes that may arise from non-selective demographic factors. Population structure was studied in a wide sample of ~1,300 coastal Douglas-fir [Pseudotsuga menziesii (Mirb.) Franco var. menziesii] trees from Washington and Oregon. This sample is being used for association mapping between cold hardiness and phenology phenotypes and single-nucleotide polymorphisms in adaptive-trait candidate genes. All trees were genotyped for 25 allozyme and six simple sequence repeat (SSR) markers using individual megagametophytes. Population structure analysis was done separately for allozyme and SSR markers, as well as for both datasets combined. The parameter of genetic differentiation (θ or F ST) was standardized to take into account high within-population variation in the SSR loci and to allow comparison with allozyme loci. Genetic distance between populations was positively and significantly correlated with geographic distance, and weak but significant clinal variation was found for a few alleles. Although the STRUCTURE simulation analysis inferred the same number of populations as used in this study and as based on previous analysis of quantitative adaptive trait variation, clustering among populations was not significant. In general, results indicated weak differentiation among populations for both allozyme and SSR loci (θ s = 0.006-0.059). The lack of pronounced population subdivision in the studied area should facilitate association mapping in this experimental population, but we recommend taking the STRUCTURE analysis and population assignments for individual trees (Q-matrix) into account in association mapping.