Cargando…

Detecting amino acid preference shifts with codon-level mutation-selection mixture models

BACKGROUND: In recent years, increasing attention has been placed on the development of phylogeny-based statistical methodologies for uncovering site-specific changes in amino acid fitness profiles over time. The few available random-effects approaches, modelling across-site variation in amino acid...

Descripción completa

Detalles Bibliográficos
Autores principales: Kazmi, S. Omar, Rodrigue, Nicolas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6390532/
https://www.ncbi.nlm.nih.gov/pubmed/30808289
http://dx.doi.org/10.1186/s12862-019-1358-7
_version_ 1783398156241731584
author Kazmi, S. Omar
Rodrigue, Nicolas
author_facet Kazmi, S. Omar
Rodrigue, Nicolas
author_sort Kazmi, S. Omar
collection PubMed
description BACKGROUND: In recent years, increasing attention has been placed on the development of phylogeny-based statistical methodologies for uncovering site-specific changes in amino acid fitness profiles over time. The few available random-effects approaches, modelling across-site variation in amino acid profiles as random variables drawn from a statistical law, either lack a mechanistic codon-level formulation, or pose significant computational challenges. RESULTS: Here, we bring together a few existing ideas to explore a simple and fast method based on a predefined finite mixture of amino acid profiles within a codon-level substitution model following the mutation-selection formulation. Our study is focused on the detection of site-specific shifts in amino acid profiles over a known sub-clade of a tree, using simulations with and without shifts over the sub-clade to study the properties of the method. Through modifications of the values of the amino acid profiles, our simulations show different levels of reliability under different forms of finite mixture models. Sites identified by our method in a real data set show obvious overlap with those identified using previous methods, with some notable differences. CONCLUSION: Overall, our results show that when a site-specific shift in amino acid profile is strongly pronounced, involving two clearly different sets of profiles, the method performs very well; but shifts between profiles that share many features are difficult to correctly identify, highlighting the challenging nature of the problem.
format Online
Article
Text
id pubmed-6390532
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-63905322019-03-11 Detecting amino acid preference shifts with codon-level mutation-selection mixture models Kazmi, S. Omar Rodrigue, Nicolas BMC Evol Biol Methodology Article BACKGROUND: In recent years, increasing attention has been placed on the development of phylogeny-based statistical methodologies for uncovering site-specific changes in amino acid fitness profiles over time. The few available random-effects approaches, modelling across-site variation in amino acid profiles as random variables drawn from a statistical law, either lack a mechanistic codon-level formulation, or pose significant computational challenges. RESULTS: Here, we bring together a few existing ideas to explore a simple and fast method based on a predefined finite mixture of amino acid profiles within a codon-level substitution model following the mutation-selection formulation. Our study is focused on the detection of site-specific shifts in amino acid profiles over a known sub-clade of a tree, using simulations with and without shifts over the sub-clade to study the properties of the method. Through modifications of the values of the amino acid profiles, our simulations show different levels of reliability under different forms of finite mixture models. Sites identified by our method in a real data set show obvious overlap with those identified using previous methods, with some notable differences. CONCLUSION: Overall, our results show that when a site-specific shift in amino acid profile is strongly pronounced, involving two clearly different sets of profiles, the method performs very well; but shifts between profiles that share many features are difficult to correctly identify, highlighting the challenging nature of the problem. BioMed Central 2019-02-26 /pmc/articles/PMC6390532/ /pubmed/30808289 http://dx.doi.org/10.1186/s12862-019-1358-7 Text en © The Author(s) 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
spellingShingle Methodology Article
Kazmi, S. Omar
Rodrigue, Nicolas
Detecting amino acid preference shifts with codon-level mutation-selection mixture models
title Detecting amino acid preference shifts with codon-level mutation-selection mixture models
title_full Detecting amino acid preference shifts with codon-level mutation-selection mixture models
title_fullStr Detecting amino acid preference shifts with codon-level mutation-selection mixture models
title_full_unstemmed Detecting amino acid preference shifts with codon-level mutation-selection mixture models
title_short Detecting amino acid preference shifts with codon-level mutation-selection mixture models
title_sort detecting amino acid preference shifts with codon-level mutation-selection mixture models
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6390532/
https://www.ncbi.nlm.nih.gov/pubmed/30808289
http://dx.doi.org/10.1186/s12862-019-1358-7
work_keys_str_mv AT kazmisomar detectingaminoacidpreferenceshiftswithcodonlevelmutationselectionmixturemodels
AT rodriguenicolas detectingaminoacidpreferenceshiftswithcodonlevelmutationselectionmixturemodels