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Inferring the number and position of changes in selective regime in a non-equilibrium mutation-selection framework

BACKGROUND: Recovering the historical patterns of selection acting on a protein coding sequence is a major goal of evolutionary biology. Mutation-selection models address this problem by explicitly modelling fixation rates as a function of site-specific amino acid fitness values.However, they are re...

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Autores principales: Ritchie, Andrew M., Stark, Tristan L., Liberles, David A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7944921/
https://www.ncbi.nlm.nih.gov/pubmed/33691618
http://dx.doi.org/10.1186/s12862-021-01770-4
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author Ritchie, Andrew M.
Stark, Tristan L.
Liberles, David A.
author_facet Ritchie, Andrew M.
Stark, Tristan L.
Liberles, David A.
author_sort Ritchie, Andrew M.
collection PubMed
description BACKGROUND: Recovering the historical patterns of selection acting on a protein coding sequence is a major goal of evolutionary biology. Mutation-selection models address this problem by explicitly modelling fixation rates as a function of site-specific amino acid fitness values.However, they are restricted in their utility for investigating directional evolution because they require prior knowledge of the locations of fitness changes in the lineages of a phylogeny. RESULTS: We apply a modified mutation-selection methodology that relaxes assumptions of equlibrium and time-reversibility. Our implementation allows us to identify branches where adaptive or compensatory shifts in the fitness landscape have taken place, signalled by a change in amino acid fitness profiles. Through simulation and analysis of an empirical data set of [Formula: see text] -lactamase genes, we test our ability to recover the position of adaptive events within the tree and successfully reconstruct initial codon frequencies and fitness profile parameters generated under the non-stationary model. CONCLUSION: We demonstrate successful detection of selective shifts and identification of the affected branch on partitions of 300 codons or more. We successfully reconstruct fitness parameters and initial codon frequencies in simulated data and demonstrate that failing to account for non-equilibrium evolution can increase the error in fitness profile estimation. We also demonstrate reconstruction of plausible shifts in amino acid fitnesses in the bacterial [Formula: see text] -lactamase family and discuss some caveats for interpretation.
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spelling pubmed-79449212021-03-11 Inferring the number and position of changes in selective regime in a non-equilibrium mutation-selection framework Ritchie, Andrew M. Stark, Tristan L. Liberles, David A. BMC Ecol Evol Methodology Article BACKGROUND: Recovering the historical patterns of selection acting on a protein coding sequence is a major goal of evolutionary biology. Mutation-selection models address this problem by explicitly modelling fixation rates as a function of site-specific amino acid fitness values.However, they are restricted in their utility for investigating directional evolution because they require prior knowledge of the locations of fitness changes in the lineages of a phylogeny. RESULTS: We apply a modified mutation-selection methodology that relaxes assumptions of equlibrium and time-reversibility. Our implementation allows us to identify branches where adaptive or compensatory shifts in the fitness landscape have taken place, signalled by a change in amino acid fitness profiles. Through simulation and analysis of an empirical data set of [Formula: see text] -lactamase genes, we test our ability to recover the position of adaptive events within the tree and successfully reconstruct initial codon frequencies and fitness profile parameters generated under the non-stationary model. CONCLUSION: We demonstrate successful detection of selective shifts and identification of the affected branch on partitions of 300 codons or more. We successfully reconstruct fitness parameters and initial codon frequencies in simulated data and demonstrate that failing to account for non-equilibrium evolution can increase the error in fitness profile estimation. We also demonstrate reconstruction of plausible shifts in amino acid fitnesses in the bacterial [Formula: see text] -lactamase family and discuss some caveats for interpretation. BioMed Central 2021-03-10 /pmc/articles/PMC7944921/ /pubmed/33691618 http://dx.doi.org/10.1186/s12862-021-01770-4 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Methodology Article
Ritchie, Andrew M.
Stark, Tristan L.
Liberles, David A.
Inferring the number and position of changes in selective regime in a non-equilibrium mutation-selection framework
title Inferring the number and position of changes in selective regime in a non-equilibrium mutation-selection framework
title_full Inferring the number and position of changes in selective regime in a non-equilibrium mutation-selection framework
title_fullStr Inferring the number and position of changes in selective regime in a non-equilibrium mutation-selection framework
title_full_unstemmed Inferring the number and position of changes in selective regime in a non-equilibrium mutation-selection framework
title_short Inferring the number and position of changes in selective regime in a non-equilibrium mutation-selection framework
title_sort inferring the number and position of changes in selective regime in a non-equilibrium mutation-selection framework
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7944921/
https://www.ncbi.nlm.nih.gov/pubmed/33691618
http://dx.doi.org/10.1186/s12862-021-01770-4
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