MHC genetic structure and divergence across populations of Chinook salmon (Oncorhynchus tshawytscha)

• Published in: Heredity Vol. 104; no. 5; pp. 449 - 459
• Main Authors: Evans, M L, Neff, B D, Heath, D D
• Format: Journal Article
• Language: English
• Published: Cham Springer International Publishing 01.05.2010; Springer Nature B.V
• Subjects: Alleles; Animals; Biodiversity; Biogeography; Biomedical and Life Sciences; Biomedicine; Comparative studies; Cytogenetics; Ecology; Evolutionary Biology; Gene Frequency; Genes, MHC Class I; Genes, MHC Class II; Genetic diversity; Genetic Loci; Genetic structure; Genetic Variation; Genetics, Population; Human Genetics; Microsatellite Repeats; Oncorhynchus tshawytscha; original-article; Pathogens; Plant Genetics and Genomics; Population genetics; Population levels; Population structure; Salmon; Salmon - genetics; British Columbia Canada; Canada; Canada, British Columbia; local adaptation; major histocompatibility complex; population genetic structure; selection; Chinook salmon
• ISSN: 0018-067X; 1365-2540; 1365-2540
• DOI: 10.1038/hdy.2009.121

The major histocompatibility complex (MHC) is thought to be under strong selection pressure because of its integral role in pathogen recognition. Consequently, patterns of MHC genetic variation should reflect selection pressures across the landscape. We examined genetic variation and population genetic structure at the MHC class I-A1 and class II-B1 exons in five Chinook salmon ( Oncorhynchus tshawytscha ) populations from two geographic regions in British Columbia, Canada. We then compared estimates of population structure at the MHC genes with neutral estimates based on microsatellites to examine the potential for local adaptation at the MHC. Chinook salmon are in decline throughout much of their native range and understanding the degree of local adaptation exhibited by the MHC may be important in conservation planning. Comparisons among populations yielded higher G′ ST estimates for the MHC class I than expected under neutrality based on the microsatellites. In contrast, the MHC class II tended to exhibit lower G′ ST values than did the microsatellites. These results suggest that across populations unique selection pressures are driving allele frequency differences at the MHC class I but that the MHC class II may be the subject of homogenizing selection. Rates of nonsynonymous versus synonymous substitutions found in codons associated within the MHC class I and II peptide-binding regions provided strong evidence of positive selection. Together, these results support the hypothesis that selection is influencing genetic variation at the MHC, but suggest that selection pressures may vary at the two classes of loci both at the sequence and population levels.