Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Perspective
  • Published:

Polygenic adaptation: a unifying framework to understand positive selection

An Author Correction to this article was published on 06 August 2020

This article has been updated

Abstract

Most adaption processes have a polygenic genetic basis, but even with the recent explosive growth of genomic data we are still lacking a unified framework describing the dynamics of selected alleles. Building on recent theoretical and empirical work we introduce the concept of adaptive architecture, which extends the genetic architecture of an adaptive trait by factors influencing its adaptive potential and population genetic principles. Because adaptation can be typically achieved by many different combinations of adaptive alleles (redundancy), we describe how two characteristics — heterogeneity among loci and non-parallelism between replicated populations — are hallmarks for the characterization of polygenic adaptation in evolving populations. We discuss how this unified framework can be applied to natural and experimental populations.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Fig. 1: Alternative adaptive paradigms: selective sweeps versus the infinitesimal model.
Fig. 2: Different approaches to characterize polygenic adaptation.
Fig. 3: Genetic redundancy and heterogeneity among loci are the main characteristics of polygenic adaptation.
Fig. 4: Different stages of polygenic adaptation.

Similar content being viewed by others

Change history

  • 06 August 2020

    An amendment to this paper has been published and can be accessed via a link at the top of the paper.

References

  1. Pritchard, J. K. & Di Rienzo, A. Adaptation — not by sweeps alone. Nat. Rev. Genet. 11, 665–667 (2010).

    CAS  PubMed  PubMed Central  Google Scholar 

  2. Pritchard, J. K., Pickrell, J. K. & Coop, G. The genetics of human adaptation: hard sweeps, soft sweeps, and polygenic adaptation. Curr. Biol. 20, R208–R215 (2010). This key paper defines the concept of polygenic adaptation.

    CAS  PubMed  PubMed Central  Google Scholar 

  3. Boyle, E. A., Li, Y. I. & Pritchard, J. K. An expanded view of complex traits: from polygenic to omnigenic. Cell 169, 1177–1186 (2017). This landmark paper introduces the omnigenic model and links quantitative genetics with molecular biology.

    CAS  PubMed  PubMed Central  Google Scholar 

  4. Csillery, K., Rodriguez-Verdugo, A., Rellstab, C. & Guillaume, F. Detecting the genomic signal of polygenic adaptation and the role of epistasis in evolution. Mol. Ecol. 27, 606–612 (2018).

    PubMed  Google Scholar 

  5. Stephan, W. Selective sweeps. Genetics 211, 5–13 (2019).

    PubMed  PubMed Central  Google Scholar 

  6. Maynard Smith, J. & Haigh, J. The hitch-hiking effect of a favourable gene. Genet. Res. 23, 23–35 (1974).

    Google Scholar 

  7. Jain, K. & Stephan, W. Modes of rapid polygenic adaptation. Mol. Biol. Evol. 34, 3169–3175 (2017).

    CAS  PubMed  Google Scholar 

  8. Hermisson, J. & Pennings, P. S. Soft sweeps: molecular population genetics of adaptation from standing genetic variation. Genetics 169, 2335–2352 (2005).

    CAS  PubMed  PubMed Central  Google Scholar 

  9. Przeworski, M., Coop, G. & Wall, J. D. The signature of positive selection on standing genetic variation. Evolution 59, 2312–2323 (2005).

    PubMed  Google Scholar 

  10. Teshima, K. M. & Przeworski, M. Directional positive selection on an allele of arbitrary dominance. Genetics 172, 713–718 (2006).

    CAS  PubMed  PubMed Central  Google Scholar 

  11. Ewing, G., Hermisson, J., Pfaffelhuber, P. & Rudolf, J. Selective sweeps for recessive alleles and for other modes of dominance. J. Math. Biol. 63, 399–431 (2011).

    CAS  PubMed  Google Scholar 

  12. Coop, G. & Ralph, P. Patterns of neutral diversity under general models of selective sweeps. Genetics 192, 205–224 (2012).

    PubMed  PubMed Central  Google Scholar 

  13. Orr, H. A. The genetic theory of adaptation: a brief history. Nat. Rev. Genet. 6, 119–127 (2005).

    CAS  PubMed  Google Scholar 

  14. Kauffman, S. & Levin, S. Towards a general theory of adaptive walks on rugged landscapes. J. Theor. Biol. 128, 11–45 (1987).

    CAS  PubMed  Google Scholar 

  15. Geritz, S. A. H., Kisdi, E., Meszena, G. & Metz, J. A. J. Evolutionarily singular strategies and the adaptive growth and branching of the evolutionary tree. Evol. Ecol. 12, 35–57 (1998).

    Google Scholar 

  16. Fisher, R. A. The correlation between relatives on the supposition of Mendelian inheritance. Trans. Roy. Soc. Edinb. 52, 339–433 (1918).

    Google Scholar 

  17. Galton, F. Natural Inheritance (MacMillan, 1889).

  18. Bulmer, M. G. Effect of selection on genetic variability. Am. Nat. 105, 201–211 (1971).

    Google Scholar 

  19. Barton, N. H. & Keightley, P. D. Understanding quantitative genetic variation. Nat. Rev. Genet. 3, 11–21 (2002).

    CAS  PubMed  Google Scholar 

  20. Turelli, M. Commentary: Fisher’s infinitesimal model: a story for the ages. Theor. Popul. Biol. 118, 46–49 (2017).

    PubMed  Google Scholar 

  21. Barton, N. H., Etheridge, A. M. & Veber, A. The infinitesimal model: definition, derivation, and implications. Theor. Popul. Biol. 118, 50–73 (2017). This paper explains the infinitesimal model using modern statistical and population genetic terminology.

    CAS  PubMed  Google Scholar 

  22. Chevin, L. M. & Hospital, F. Selective sweep at a quantitative trait locus in the presence of background genetic variation. Genetics 180, 1645–1660 (2008). This study is one of the first to investigate whether genomic sweep signatures are also possible for polygenic adaptation.

    PubMed  PubMed Central  Google Scholar 

  23. Jain, K. & Stephan, W. Rapid adaptation of a polygenic trait after a sudden environmental shift. Genetics 206, 389–406 (2017). This paper provides analytical approaches to describe cases of sweep signatures for large-effect alleles and small allele shifts for small-effect loci during polygenic adaptation.

    PubMed  PubMed Central  Google Scholar 

  24. Pavlidis, P. & Alachiotis, N. A survey of methods and tools to detect recent and strong positive selection. J. Biol. Res. 24, 7 (2017).

    Google Scholar 

  25. Vitti, J. J., Grossman, S. R. & Sabeti, P. C. Detecting natural selection in genomic data. Annu. Rev. Genet. 47, 97–120 (2013).

    CAS  PubMed  Google Scholar 

  26. Coop, G., Witonsky, D., Di Rienzo, A. & Pritchard, J. K. Using environmental correlations to identify loci underlying local adaptation. Genetics 185, 1411–1423 (2010).

    CAS  PubMed  PubMed Central  Google Scholar 

  27. Hancock, A. M. et al. Adaptations to climate-mediated selective pressures in humans. PLoS Genet. 7, e1001375 (2011).

    CAS  PubMed  PubMed Central  Google Scholar 

  28. Hancock, A. M. et al. Adaptation to climate across the Arabidopsis thaliana genome. Science 334, 83–86 (2011).

    CAS  PubMed  Google Scholar 

  29. Daub, J. T. et al. Evidence for polygenic adaptation to pathogens in the human genome. Mol. Biol. Evol. 30, 1544–1558 (2013).

    CAS  PubMed  Google Scholar 

  30. Gouy, A., Daub, J. T. & Excoffier, L. Detecting gene subnetworks under selection in biological pathways. Nucleic Acids Res. 45, e149 (2017).

    PubMed  PubMed Central  Google Scholar 

  31. Bycroft, C. et al. The UK Biobank resource with deep phenotyping and genomic data. Nature 562, 203–209 (2018).

    CAS  PubMed  PubMed Central  Google Scholar 

  32. Robinson, M. R. et al. Population genetic differentiation of height and body mass index across Europe. Nat. Genet. 47, 1357–1362 (2015).

    CAS  PubMed  PubMed Central  Google Scholar 

  33. Lohmueller, K. E., Mauney, M. M., Reich, D. & Braverman, J. M. Variants associated with common disease are not unusually differentiated in frequency across populations. Am. J. Hum. Genet. 78, 130–136 (2006).

    CAS  PubMed  Google Scholar 

  34. Sella, G. & Barton, N. H. Thinking about the evolution of complex traits in the era of genome-wide association studies. Annu. Rev. Genom. Hum. Genet. 20, 461–493 (2019). This comprehensive review discusses the connection between GWAS and polygenic adaptation.

    CAS  Google Scholar 

  35. Turchin, M. C. et al. Evidence of widespread selection on standing variation in Europe at height-associated SNPs. Nat. Genet. 44, 1015–1019 (2012).

    CAS  PubMed  PubMed Central  Google Scholar 

  36. Guo, J. et al. Global genetic differentiation of complex traits shaped by natural selection in humans. Nat. Commun. 9, 1865 (2018).

    PubMed  PubMed Central  Google Scholar 

  37. Field, Y. et al. Detection of human adaptation during the past 2000 years. Science 354, 760–764 (2016). This paper introduces the singleton density score to detect polygenic adaptation.

    CAS  PubMed  PubMed Central  Google Scholar 

  38. Meuwissen, T. H. E., Hayes, B. J. & Goddard, M. E. Prediction of total genetic value using genome-wide dense marker maps. Genetics 157, 1819–1829 (2001).

    CAS  PubMed  PubMed Central  Google Scholar 

  39. Berg, J. J. & Coop, G. A population genetic signal of polygenic adaptation. PLoS Genet. 10, e1004412 (2014). This paper presents a key method to detect polygenic adaptation from GWAS data.

    PubMed  PubMed Central  Google Scholar 

  40. Novembre, J. & Barton, N. H. Tread lightly interpreting polygenic tests of selection. Genetics 208, 1351–1355 (2018).

    PubMed  PubMed Central  Google Scholar 

  41. Ferrero-Serrano, A. & Assmann, S. M. Phenotypic and genome-wide association with the local environment of Arabidopsis. Nat. Ecol. Evol. 3, 274–285 (2019).

    PubMed  Google Scholar 

  42. Yeaman, S. et al. Convergent local adaptation to climate in distantly related conifers. Science 353, 1431–1433 (2016). This paper is an empirical demonstration of convergent local adaptation between two distantly related tree species confronted with the same adaptive challenge.

    CAS  PubMed  Google Scholar 

  43. Gazal, S. et al. Linkage disequilibrium-dependent architecture of human complex traits shows action of negative selection. Nat. Genet. 49, 1421–1427 (2017).

    CAS  PubMed  PubMed Central  Google Scholar 

  44. Zeng, J. et al. Signatures of negative selection in the genetic architecture of human complex traits. Nat. Genet. 50, 746–753 (2018).

    CAS  PubMed  Google Scholar 

  45. Fisher, R. A. The Genetical Theory of Natural Selection (Clarendon Press, 1930).

  46. Chevin, L. M., Martin, G. & Lenormand, T. Fisher’s model and the genomics of adaptation: restricted pleiotropy, heterogenous mutation, and parallel evolution. Evolution 64, 3213–3231 (2010).

    PubMed  Google Scholar 

  47. Hansen, T. F. & Houle, D. Measuring and comparing evolvability and constraint in multivariate characters. J. Evolut. Biol. 21, 1201–1219 (2008).

    CAS  Google Scholar 

  48. Jones, A. G., Arnold, S. J. & Bürger, R. Stability of the G-matrix in a population experiencing pleiotropic mutation, stabilizing selection, and genetic drift. Evolution 57, 1747–1760 (2003).

    PubMed  Google Scholar 

  49. Yeaman, S., Gerstein, A. C., Hodgins, K. A. & Whitlock, M. C. Quantifying how constraints limit the diversity of viable routes to adaptation. PLoS Genet. 14, e1007717 (2018). This paper develops an index to quantify the amount of observed repeatability relative to theoretical expectations.

    PubMed  PubMed Central  Google Scholar 

  50. Simons, Y. B., Bullaughey, K., Hudson, R. R. & Sella, G. A population genetic interpretation of GWAS findings for human quantitative traits. PLoS Biol. 16, e2002985 (2018).

    PubMed  PubMed Central  Google Scholar 

  51. Carlson, C. S. et al. Generalization and dilution of association results from European GWAS in populations of non-European ancestry: the PAGE study. PLoS Biol. 11, e1001661 (2013).

    CAS  PubMed  PubMed Central  Google Scholar 

  52. Erbe, M. et al. Improving accuracy of genomic predictions within and between dairy cattle breeds with imputed high-density single nucleotide polymorphism panels. J. Dairy. Sci. 95, 4114–4129 (2012).

    CAS  PubMed  Google Scholar 

  53. de Roos, A. P., Hayes, B. J. & Goddard, M. E. Reliability of genomic predictions across multiple populations. Genetics 183, 1545–1553 (2009).

    PubMed  PubMed Central  Google Scholar 

  54. Guo, Z. et al. The impact of population structure on genomic prediction in stratified populations. Theor. Appl. Genet. 127, 749–762 (2014).

    PubMed  Google Scholar 

  55. Haworth, S. et al. Apparent latent structure within the UK Biobank sample has implications for epidemiological analysis. Nat. Commun. 10, 333 (2019).

    PubMed  PubMed Central  Google Scholar 

  56. Berg, J. J. et al. Reduced signal for polygenic adaptation of height in UK Biobank. eLife 8, e39725 (2019).

    PubMed  PubMed Central  Google Scholar 

  57. Sohail, M. et al. Polygenic adaptation on height is overestimated due to uncorrected stratification in genome-wide association studies. eLife 8, e39702 (2019).

    PubMed  PubMed Central  Google Scholar 

  58. Beissinger, T. et al. A simple test identifies selection on complex traits. Genetics 209, 321–333 (2018).

    CAS  PubMed  PubMed Central  Google Scholar 

  59. Racimo, F., Berg, J. J. & Pickrell, J. K. Detecting polygenic adaptation in admixture graphs. Genetics 208, 1565–1584 (2018).

    PubMed  PubMed Central  Google Scholar 

  60. Hansen, T. F. The evolution of genetic architecture. Annu. Rev. Ecol. Evol. S 37, 123–157 (2006).

    Google Scholar 

  61. Carlborg, O. & Haley, C. S. Epistasis: too often neglected in complex trait studies? Nat. Rev. Genet. 5, 618–625 (2004).

    CAS  PubMed  Google Scholar 

  62. Goldstein, D. B. & Holsinger, K. E. Maintenance of polygenic variation in spatially structured populations: roles for local mating and genetic redundancy. Evolution 46, 412–429 (1992).

    PubMed  Google Scholar 

  63. Yeaman, S. Local adaptation by alleles of small effect. Am. Nat. 186, S74–S89 (2015).

    PubMed  Google Scholar 

  64. Kopp, M. & Hermisson, J. Adaptation of a quantitative trait to a moving optimum. Genetics 176, 715–719 (2007).

    CAS  PubMed  PubMed Central  Google Scholar 

  65. Matuszewski, S., Hermisson, J. & Kopp, M. Catch me if you can: adaptation from standing genetic variation to a moving phenotypic optimum. Genetics 200, 1255–1274 (2015).

    PubMed  PubMed Central  Google Scholar 

  66. Jain, K. & Devi, A. Polygenic adaptation in changing environments. EPL 123, 48002 (2018).

    Google Scholar 

  67. Stetter, M. G., Thornton, K. & Ross-Ibarra, J. Genetic architecture and selective sweeps after polygenic adaptation to distant trait optima. PLoS Genet. 14, e1007794 (2018).

    PubMed  PubMed Central  Google Scholar 

  68. Orr, H. A. Adaptation and the cost of complexity. Evolution 54, 13–20 (2000).

    CAS  PubMed  Google Scholar 

  69. Wagner, G. P. & Altenberg, L. Perspective: complex adaptations and the evolution of evolvability. Evolution 50, 967–976 (1996).

    PubMed  Google Scholar 

  70. Chevin, L. M. Selective sweep at a QTL in a randomly fluctuating environment. Genetics 213, 987–1005 (2019).

    PubMed  PubMed Central  Google Scholar 

  71. Pavlidis, P., Metzler, D. & Stephan, W. Selective sweeps in multilocus models of quantitative traits. Genetics 192, 225–239 (2012).

    PubMed  PubMed Central  Google Scholar 

  72. Wollstein, A. & Stephan, W. Adaptive fixation in two-locus models of stabilizing selection and genetic drift. Genetics 198, 685–697 (2014).

    PubMed  PubMed Central  Google Scholar 

  73. Franssen, S. U., Kofler, R. & Schlötterer, C. Uncovering the genetic signature of quantitative trait evolution with replicated time series data. Heredity 118, 42–51 (2017). This paper studies genomic signatures of polygenic adaptation in small, replicated experimental populations.

    CAS  PubMed  Google Scholar 

  74. Thornton, K. R. Polygenic adaptation to an environmental shift: temporal dynamics of variation under Gaussian stabilizing selection and additive effects on a single trait. Genetics (2019). This study presents a comprehensive simulation of polygenic adaptation of a single additive trait.

  75. de Vladar, H. P. & Barton, N. Stability and response of polygenic traits to stabilizing selection and mutation. Genetics 197, 749–767 (2014).

    PubMed  PubMed Central  Google Scholar 

  76. Jain, K. & Stephan, W. Response of polygenic traits under stabilizing selection and mutation when loci have unequal effects. G3 5, 1065–1074 (2015).

    PubMed  PubMed Central  Google Scholar 

  77. Höllinger, I., Pennings, P. S. & Hermisson, J. Polygenic adaptation: from sweeps to subtle frequency shifts. PLoS Genet. 15, e1008035 (2019). This paper presents an analytical framework to describe the adaptive architecture of a polygenic trait.

    PubMed  PubMed Central  Google Scholar 

  78. Hayward, L. K. & Sella, G. Polygenic adaptation after a sudden change in environment. bioRxiv (2019). This paper presents an analytical description of the adaptation process for a highly polygenic trait.

  79. Sachdeva, H. & Barton, N. H. Replicability of introgression under linked, polygenic selection. Genetics 210, 1411–1427 (2018).

    PubMed  PubMed Central  Google Scholar 

  80. Sachdeva, H. & Barton, N. H. Introgression of a block of genome under infinitesimal selection. Genetics 209, 1279–1303 (2018). This paper models adaptation for the infinitesimal model with linkage and finds that this can lead to large frequency changes.

    PubMed  PubMed Central  Google Scholar 

  81. Robertson, A. in Proc. Int. Conf. Quant. Genet. (eds, E. Pollak, O. Kempthorne & T. B. Bail) 307–322 (Iowa State Univ. Press, 1977).

  82. Ralph, P. & Coop, G. Parallel adaptation: one or many waves of advance of an advantageous allele? Genetics 186, 647–668 (2010).

    PubMed  PubMed Central  Google Scholar 

  83. Ralph, P. L. & Coop, G. The role of standing variation in geographic convergent adaptation. Am. Nat. 186, S5–S23 (2015).

    PubMed  PubMed Central  Google Scholar 

  84. Ralph, P. L. & Coop, G. Convergent evolution during local adaptation to patchy landscapes. PLoS Genet. 11, e1005630 (2015).

    PubMed  PubMed Central  Google Scholar 

  85. Paulose, J., Hermisson, J. & Hallatschek, O. Spatial soft sweeps: patterns of adaptation in populations with long-range dispersal. PLoS Genet. 15, e1007936 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  86. Barton, N. H. Clines in polygenic traits. Genet. Res. 74, 223–236 (1999).

    CAS  PubMed  Google Scholar 

  87. Jaccard, P. Louis de distribution florale dans la zone alpine. Bull. Soc. Vaud. Sci. Nat. 38, 69–130 (1902).

    Google Scholar 

  88. Barghi, N. et al. Genetic redundancy fuels polygenic adaptation in Drosophila. PLoS Biol. 17, e3000128 (2019). This paper provides empirical proof that polygenic adaptation can be detected in sufficiently well-replicated experimental evolution studies.

    CAS  PubMed  PubMed Central  Google Scholar 

  89. Nene, N. R., Dunham, A. S. & Illingworth, C. J. R. Inferring fitness effects from time-resolved sequence data with a delay-deterministic model. Genetics 209, 255–264 (2018).

    PubMed  PubMed Central  Google Scholar 

  90. Martin, A. & Orgogozo, V. The Loci of repeated evolution: a catalog of genetic hotspots of phenotypic variation. Evolution 67, 1235–1250 (2013).

    CAS  PubMed  Google Scholar 

  91. Stern, D. L. The genetic causes of convergent evolution. Nat. Rev. Genet. 14, 751–764 (2013).

    CAS  PubMed  Google Scholar 

  92. Conte, G. L. et al. Extent of QTL reuse during repeated phenotypic divergence of sympatric threespine stickleback. Genetics 201, 1189–1200 (2015). This paper presents an innovative approach using QTL mapping to explore redundancy.

    PubMed  PubMed Central  Google Scholar 

  93. Harris, R. B. et al. The population genetics of crypsis in vertebrates: recent insights from mice, hares, and lizards. Heredity 124, 1–14 (2019).

    PubMed  PubMed Central  Google Scholar 

  94. Catania, F. et al. World-wide survey of an Accord insertion and its association with DDT resistance in Drosophila melanogaster. Mol. Ecol. 13, 2491–2504 (2004).

    CAS  PubMed  Google Scholar 

  95. Schlenke, T. A. & Begun, D. J. Strong selective sweep associated with a transposon insertion in Drosophila simulans. Proc. Natl Acad. Sci. USA 101, 1626–1631 (2004).

    CAS  PubMed  PubMed Central  Google Scholar 

  96. Colosimo, P. F. et al. Widespread parallel evolution in sticklebacks by repeated fixation of Ectodysplasin alleles. Science 307, 1928–1933 (2005). This classic study shows that the same allele is independently selected in many river populations of sticklebacks.

    CAS  PubMed  Google Scholar 

  97. Adrion, J. R., Hahn, M. W. & Cooper, B. S. Revisiting classic clines in Drosophila melanogaster in the age of genomics. Trends Genet. 31, 434–444 (2015).

    CAS  PubMed  PubMed Central  Google Scholar 

  98. Yi, X. et al. Sequencing of 50 human exomes reveals adaptation to high altitude. Science 329, 75–78 (2010).

    CAS  PubMed  PubMed Central  Google Scholar 

  99. Crawford, J. E. et al. Natural selection on genes related to cardiovascular health in high-altitude adapted andeans. Am. J. Hum. Genet. 101, 752–767 (2017).

    CAS  PubMed  PubMed Central  Google Scholar 

  100. Bigham, A. et al. Identifying signatures of natural selection in tibetan and andean populations using dense genome scan data. PLoS Genet. 6, e1001116 (2010).

    PubMed  PubMed Central  Google Scholar 

  101. Keller, I., Alexander, J. M., Holderegger, R. & Edwards, P. J. Widespread phenotypic and genetic divergence along altitudinal gradients in animals. J. Evolut. Biol. 26, 2527–2543 (2013).

    CAS  Google Scholar 

  102. Halbritter, A. H. et al. Trait differentiation and adaptation of plants along elevation gradients. J. Evolut. Biol. 31, 784–800 (2018).

    Google Scholar 

  103. Alexander, H. J., Taylor, J. S., Wu, S. S. & Breden, F. Parallel evolution and vicariance in the guppy (Poecilia reticulata) over multiple spatial and temporal scales. Evolution 60, 2352–2369 (2006).

    CAS  PubMed  Google Scholar 

  104. Hendry, A. P., Kelly, M. L., Kinnison, M. T. & Reznick, D. N. Parallel evolution of the sexes? Effects of predation and habitat features on the size and shape of wild guppies. J. Evolut. Biol. 19, 741–754 (2006).

    CAS  Google Scholar 

  105. Reznick, D. N. & Bryga, H. Life-history evolution in guppies (Poecilia Reticulata): 1. phenotypic and genetic changes in an introduction experiment. Evolution 41, 1370–1385 (1987).

    PubMed  Google Scholar 

  106. Jones, F. C. et al. The genomic basis of adaptive evolution in threespine sticklebacks. Nature 484, 55–61 (2012).

    CAS  PubMed  PubMed Central  Google Scholar 

  107. Hohenlohe, P. A. et al. Population genomics of parallel adaptation in threespine stickleback using sequenced RAD tags. PLoS Genet. 6, e1000862 (2010).

    PubMed  PubMed Central  Google Scholar 

  108. Jones, F. C. et al. A genome-wide SNP genotyping array reveals patterns of global and repeated species-pair divergence in sticklebacks. Curr. Biol. 22, 83–90 (2012).

    CAS  PubMed  Google Scholar 

  109. Stuart, Y. E. et al. Contrasting effects of environment and genetics generate a continuum of parallel evolution. Nat. Ecol. Evol. 1, 158 (2017).

    PubMed  Google Scholar 

  110. Ficetola, G. F. et al. DNA from lake sediments reveals long-term ecosystem changes after a biological invasion. Sci. Adv. 4, eaar4292 (2018).

    PubMed  PubMed Central  Google Scholar 

  111. Hairston, N. G. et al. Lake ecosystems — rapid evolution revealed by dormant eggs. Nature 401, 446–446 (1999).

    Google Scholar 

  112. Marques, D. A., Jones, F. C., Di Palma, F., Kingsley, D. M. & Reimchen, T. E. Experimental evidence for rapid genomic adaptation to a new niche in an adaptive radiation. Nat. Ecol. Evol. 2, 1128–1138 (2018).

    PubMed  PubMed Central  Google Scholar 

  113. Burke, M. K. et al. Genome-wide analysis of a long-term evolution experiment with Drosophila. Nature 467, 587–590 (2010).

    CAS  PubMed  Google Scholar 

  114. Schlötterer, C., Tobler, R., Kofler, R. & Nolte, V. Sequencing pools of individuals — mining genome-wide polymorphism data without big funding. Nat. Rev. Genet. 15, 749–763 (2014).

    PubMed  Google Scholar 

  115. Kelly, J. K. & Hughes, K. A. Pervasive linked selection and intermediate-frequency alleles are implicated in an evolve-and-resequencing experiment of Drosophila simulans. Genetics 211, 943–961 (2019).

    CAS  PubMed  Google Scholar 

  116. Burke, M. K., Liti, G. & Long, A. D. Standing genetic variation drives repeatable experimental evolution in outcrossing populations of Saccharomyces cerevisiae. Mol. Biol. Evol. 31, 3228–3239 (2014).

    CAS  PubMed  PubMed Central  Google Scholar 

  117. Graves, J. L. Jr et al. Genomics of parallel experimental evolution in Drosophila. Mol. Biol. Evol. 34, 831–842 (2017). This paper presents an evolve and resequence study with a surprising level of parallel evolution on the genomic and phenotypic levels.

    CAS  PubMed  PubMed Central  Google Scholar 

  118. Mallard, F., Nolte, V., Tobler, R., Kapun, M. & Schlötterer, C. A simple genetic basis of adaptation to a novel thermal environment results in complex metabolic rewiring in Drosophila. Genome Biol. 19, 119 (2018).

    PubMed  PubMed Central  Google Scholar 

  119. Sikkink, K. L., Reynolds, R. M., Ituarte, C. M., Cresko, W. A. & Phillips, P. C. Environmental and evolutionary drivers of the modular gene regulatory network underlying phenotypic plasticity for stress resistance in the nematode caenorhabditis remanei. G3 9, 969–982 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  120. Teotonio, H., Estes, S., Phillips, P. C. & Baer, C. F. Experimental evolution with Caenorhabditis nematodes. Genetics 206, 691–716 (2017).

    PubMed  PubMed Central  Google Scholar 

  121. Kosheleva, K. & Desai, M. M. Recombination alters the dynamics of adaptation on standing variation in laboratory yeast populations. Mol. Biol. Evol. 35, 180–201 (2018). This study of experimental evolution with recombinants of two yeast strains suggests the presence of many contributing loci, which continue to segregate during the entire experiment.

    CAS  PubMed  Google Scholar 

  122. Linnen, C. R., Kingsley, E. P., Jensen, J. D. & Hoekstra, H. E. On the origin and spread of an adaptive allele in deer mice. Science 325, 1095–1098 (2009).

    CAS  PubMed  PubMed Central  Google Scholar 

  123. Barrett, R. D. H. et al. Linking a mutation to survival in wild mice. Science 363, 499–504 (2019).

    CAS  PubMed  Google Scholar 

  124. Steiner, C. C., Rompler, H., Boettger, L. M., Schoneberg, T. & Hoekstra, H. E. The genetic basis of phenotypic convergence in beach mice: similar pigment patterns but different genes. Mol. Biol. Evol. 26, 35–45 (2009).

    CAS  PubMed  Google Scholar 

  125. Hauser, M. T., Harr, B. & Schlötterer, C. Trichome distribution in Arabidopsis thaliana and its close relative Arabidopsis lyrata: molecular analysis of the candidate gene GLABROUS1. Mol. Biol. Evol. 18, 1754–1763 (2001).

    CAS  PubMed  Google Scholar 

  126. Hilscher, J., Schlötterer, C. & Hauser, M. T. A single amino acid replacement in ETC2 shapes trichome patterning in natural Arabidopsis populations. Curr. Biol. 19, 1747–1751 (2009).

    CAS  PubMed  PubMed Central  Google Scholar 

  127. Daborn, P. J. et al. A single p450 allele associated with insecticide resistance in Drosophila. Sci. 297, 2253–2256 (2002).

    CAS  Google Scholar 

  128. Crow, J. F. Genetics of insect resistance to chemicals. Annu. Rev. Entomol. 2, 227–246 (1957).

    CAS  Google Scholar 

  129. Ffrench-Constant, R. H. The molecular genetics of insecticide resistance. Genetics 194, 807–815 (2013).

    CAS  PubMed  PubMed Central  Google Scholar 

  130. McKenzie, J. A., Parker, A. G. & Yen, J. L. Polygenic and single gene responses to selection for resistance to diazinon in Lucilia cuprina. Genetics 130, 613–620 (1992).

    CAS  PubMed  PubMed Central  Google Scholar 

  131. Kreiner, J. M. et al. Multiple modes of convergent adaptation in the spread of glyphosate-resistant Amaranthus tuberculatus. Proc. Natl Acad. Sci. USA 116, 21076–21084 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  132. Delye, C., Jasieniuk, M. & Le Corre, V. Deciphering the evolution of herbicide resistance in weeds. Trends Genet. 29, 649–658 (2013).

    CAS  PubMed  Google Scholar 

  133. Studer, A., Zhao, Q., Ross-Ibarra, J. & Doebley, J. Identification of a functional transposon insertion in the maize domestication gene tb1. Nat. Genet. 43, 1160–1163 (2011).

    CAS  PubMed  PubMed Central  Google Scholar 

  134. Wang, R. L., Stec, A., Hey, J., Lukens, L. & Doebley, J. The limits of selection during maize domestication. Nature 398, 236–239 (1999).

    CAS  PubMed  Google Scholar 

  135. Studer, A. J., Wang, H. & Doebley, J. F. Selection during maize domestication targeted a gene network controlling plant and inflorescence architecture. Genetics 207, 755–765 (2017).

    CAS  PubMed  PubMed Central  Google Scholar 

  136. Teotonio, H., Chelo, I. M., Bradic, M., Rose, M. R. & Long, A. D. Experimental evolution reveals natural selection on standing genetic variation. Nat. Genet. 41, 251–257 (2009).

    CAS  PubMed  Google Scholar 

  137. Teotonio, H. & Rose, M. R. Perspective: reverse evolution. Evolution 55, 653–660 (2001).

    CAS  PubMed  Google Scholar 

  138. Faria, V. G., Martins, N. E., Schlotterer, C. & Sucena, E. Readapting to DCV infection without Wolbachia: frequency changes of Drosophila antiviral alleles can replace endosymbiont protection. Genome Biol. Evol. 10, 1783–1791 (2018).

    CAS  PubMed  PubMed Central  Google Scholar 

  139. Martins, N. E. et al. Host adaptation to viruses relies on few genes with different cross-resistance properties. Proc. Natl Acad. Sci. USA 111, 5938–5943 (2014).

    CAS  PubMed  PubMed Central  Google Scholar 

  140. Huerta-Sanchez, E. et al. Genetic signatures reveal high-altitude adaptation in a set of Ethiopian populations. Mol. Biol. Evol. 30, 1877–1888 (2013).

    CAS  PubMed  PubMed Central  Google Scholar 

  141. Beall, C. M. Two routes to functional adaptation: Tibetan and Andean high-altitude natives. Proc. Natl Acad. Sci. USA 104, 8655–8660 (2007).

    CAS  PubMed  PubMed Central  Google Scholar 

  142. Lande, R. & Arnold, S. J. The measurement of selection on correlated characters. Evolution 37, 1210–1226 (1983).

    PubMed  Google Scholar 

  143. Rajpurohit, S., Parkash, R. & Ramniwas, S. Body melanization and its adaptive role in thermoregulation and tolerance against desiccating conditions in Drosophila. Entomol. Res. 38, 49–60 (2008).

    Google Scholar 

  144. Willmer, P. G. & Unwin, D. M. Field analyses of insect heat budgets — reflectance, size and heating rates. Oecologia 50, 250–255 (1981).

    CAS  PubMed  Google Scholar 

  145. Jaksic, A. M. et al. Neuronal function and dopamine signaling evolve at high temperature in Drosophila. Mol. Biol. Evol. https://doi.org/10.1093/molbev/msaa116 (2020).

    Article  PubMed  Google Scholar 

Download references

Acknowledgements

C.S. and J.H. are supported by various Austrian Science Fund (FWF) grants (W-1225-B20, P27630-B20, P29133-B29). Thanks to S. Allen, N. Barton, S.-K. Hsu, R. Kofler and T. MacKay for discussion and feedback on earlier versions of the manuscript.

Author information

Authors and Affiliations

Authors

Contributions

The authors contributed equally to all aspects of the article.

Corresponding authors

Correspondence to Joachim Hermisson or Christian Schlötterer.

Ethics declarations

Competing interests

The authors declare no competing interests.

Additional information

Peer review information

Nature Reviews Genetics thanks T. Mitchell Olds and the other, anonymous, reviewer(s) for their contribution to the peer review of this work.

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Glossary

Adaptive architecture

The measure of the probability that alleles contribute to adaptation. Adaptive architecture extends the genetic architecture by including further factors that influence the adaptive potential.

Adaptive introgression

New, favourable alleles are introduced into a population by migration.

Admixture graph

A representation of the divergence and admixture between populations.

Clines

Spatial patterns of allele frequency differences, which are maintained by a spatial selection gradient.

Common garden experiments

Experiments that, in order to control for the effects of the environment on phenotypes, measure the phenotypes of different genotypes in the same/similar environments.

Epistasis

Interaction between genes in a non-additive way.

Genetic architecture

Information about genes, with their associated effect sizes and patterns of pleiotropy, epistasis and dominance.

Genetic basis

The set of all loci contributing to a trait, but without reference to effect sizes or pleiotropy, epistasis or dominance.

Genetic drift

A stochastic process arising from the random sampling of gametes contributing to the next generation. In small populations, genetic drift can be strong and results in large, non-directional allele frequency changes.

Genome-wide association studies

(GWAS). A genetic technique that identifies statistically significant associations between phenotypes and underlying genetic variants. GWAS are particularly powerful, because they take advantage of recombination events that occurred historically in the focal population.

Infinitesimal model

The phenotype is determined by a very large (infinite) number of alleles, each with a very small effect, and by the environment.

Mutation–selection balance

An equilibrium situation for a population close to an adaptive optimum. The same number of new deleterious alleles are introduced into the population by mutation as are removed by purifying selection.

Non-synonymous SNPs

Single-nucleotide polymorphisms (SNPs) in protein-coding genes that result in an amino acid replacement.

Parallelism

(Also known as convergence or repeatability). Replicate populations reach the same trait values using the same set of alleles; non-parallelism is the possible consequence of redundancy. Parallelism has been also described for asexual microorganisms, where the same mutations are independently acquired in replicate populations.

Pleiotropy

A single gene affects multiple traits.

Polygenic traits

(Also known as complex traits). Quantitatively variable phenotypes that are affected by many contributing loci and the environment.

Purifying selection

Removal of deleterious alleles from a population.

Quantitative trait locus (QTL) mapping

A genetic mapping technique that relies on recombination events that occurred during the experiment.

Quantitative traits

Traits with a continuous distribution of phenotypes with a large number of contributing alleles.

Redundancy

Different combinations of alleles produce the same phenotypic value.

Selective sweeps

Classic selection signatures in molecular population genetics describing a pattern of reduced DNA polymorphism around the site of a recently fixed beneficial allele.

Singleton density score

A test statistic to detect selection based on the distance of singleton single-nucleotide polymorphisms nearest to the focal variant.

Soft sweeps

Different alleles at the same locus are favoured and contribute to adaptation. They can either be generated by recurrent mutations or they segregate in the population before the adaptive episode starts.

Stabilizing selection

Selection favours individuals with an intermediate trait value.

Standing genetic variation

Polymorphic sites segregating in a natural population.

Swamping

Beneficial alleles are driven to extinction by immigration of non-favoured alleles.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Barghi, N., Hermisson, J. & Schlötterer, C. Polygenic adaptation: a unifying framework to understand positive selection. Nat Rev Genet 21, 769–781 (2020). https://doi.org/10.1038/s41576-020-0250-z

Download citation

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/s41576-020-0250-z

This article is cited by

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing