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Population genetics of polymorphism and divergence in rapidly evolving populations

Matthew J. Melissa, View ORCID ProfileBenjamin H. Good, Daniel S. Fisher, Michael M. Desai
doi: https://doi.org/10.1101/2021.06.28.450258
Matthew J. Melissa
1Department of Organismic and Evolutionary Biology, Department of Physics, Quantitative Biology Initiative, and NSF-Simons Center for Mathematical and Statistical Analysis of Biology, Harvard University
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Benjamin H. Good
2Department of Applied Physics and Department of Bioengineering, Stanford University
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  • ORCID record for Benjamin H. Good
Daniel S. Fisher
2Department of Applied Physics and Department of Bioengineering, Stanford University
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Michael M. Desai
1Department of Organismic and Evolutionary Biology, Department of Physics, Quantitative Biology Initiative, and NSF-Simons Center for Mathematical and Statistical Analysis of Biology, Harvard University
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  • For correspondence: mdesai@oeb.harvard.edu
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Abstract

In rapidly evolving populations, numerous beneficial and deleterious mutations can arise and segregate within a population at the same time. In this regime, evolutionary dynamics cannot be analyzed using traditional population genetic approaches that assume that sites evolve independently. Instead, the dynamics of many loci must be analyzed simultaneously. Recent work has made progress by first analyzing the fitness variation within a population, and then studying how individual lineages interact with this traveling fitness wave. However, these “traveling wave” models have previously been restricted to extreme cases where selection on individual mutations is either much faster or much slower than the typical coalescent timescale Tc. In this work, we show how the traveling wave framework can be extended to intermediate regimes in which the scaled fitness effects of mutations (Tcs) are neither large nor small compared to one. This enables us to describe the dynamics of populations subject to a wide range of fitness effects, and in particular, in cases where it is not immediately clear which mutations are most important in shaping the dynamics and statistics of genetic diversity. We use this approach to derive new expressions for the fixation probabilities and site frequency spectra of mutations as a function of their scaled fitness effects, along with related results for the coalescent timescale Tc and the rate of adaptation or Muller’s ratchet. We find that competition between linked mutations can have a dramatic impact on the proportions of neutral and selected polymorphisms, which is not simply summarized by the scaled selection coefficient Tcs. We conclude by discussing the implications of these results for population genetic inferences.

Competing Interest Statement

The authors have declared no competing interest.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-NC 4.0 International license.
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Posted June 30, 2021.
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Population genetics of polymorphism and divergence in rapidly evolving populations
Matthew J. Melissa, Benjamin H. Good, Daniel S. Fisher, Michael M. Desai
bioRxiv 2021.06.28.450258; doi: https://doi.org/10.1101/2021.06.28.450258
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Population genetics of polymorphism and divergence in rapidly evolving populations
Matthew J. Melissa, Benjamin H. Good, Daniel S. Fisher, Michael M. Desai
bioRxiv 2021.06.28.450258; doi: https://doi.org/10.1101/2021.06.28.450258

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