The maintenance of standing genetic variation: Gene flow vs. selective neutrality in Atlantic stickleback fish

• Published in: Molecular ecology Vol. 31; no. 3; pp. 811 - 821
• Main Authors: Haenel, Quiterie, Guerard, Laurent, MacColl, Andrew D. C., Berner, Daniel
• Format: Journal Article
• Language: English
• Published: England Blackwell Publishing Ltd 01-02-2022; John Wiley and Sons Inc
• Subjects: Acidic lakes; Adaptation; allele frequency; ancestor; Animals; evolutionary genomics; Fish; Gasterosteus aculeatus; Gene Flow; Gene sequencing; Genetic diversity; Genetic variance; Genetic Variation; Genome; Habitats; Hybridization; Maintenance; migration–selection balance; North Uist; Nucleotide sequence; Original; ORIGINAL ARTICLES; Population genetics; Populations; purifying selection; Quantitative genetics; Selection, Genetic; Smegmamorpha - genetics; whole‐genome sequencing; evolutionary genomics; purifying selection; whole-genome sequencing; ancestor; North Uist; migration-selection balance; Gasterosteus aculeatus; allele frequency
• ISSN: 0962-1083; 1365-294X
• DOI: 10.1111/mec.16269

Adaptation to derived habitats often occurs from standing genetic variation. The maintenance within ancestral populations of genetic variants favourable in derived habitats is commonly ascribed to long‐term antagonism between purifying selection and gene flow resulting from hybridization across habitats. A largely unexplored alternative idea based on quantitative genetic models of polygenic adaptation is that variants favoured in derived habitats are neutral in ancestral populations when their frequency is relatively low. To explore the latter, we first identify genetic variants important to the adaptation of threespine stickleback fish (Gasterosteus aculeatus) to a rare derived habitat—nutrient‐depleted acidic lakes—based on whole‐genome sequence data. Sequencing marine stickleback from six locations across the Atlantic Ocean then allows us to infer that the frequency of these derived variants in the ancestral habitat is unrelated to the likely opportunity for gene flow of these variants from acidic‐adapted populations. This result is consistent with the selective neutrality of derived variants within the ancestor. Our study thus supports an underappreciated explanation for the maintenance of standing genetic variation, and calls for a better understanding of the fitness consequences of adaptive variation across habitats and genomic backgrounds.