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A Spatially Explicit Model of Stabilizing Selection for Improving Phylogenetic Inference

Ultraconserved elements (UCEs) are stretches of hundreds of nucleotides with highly conserved cores flanked by variable regions. Although the selective forces responsible for the preservation of UCEs are unknown, they are nonetheless believed to contain phylogenetically meaningful information from d...

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Autores principales: Beaulieu, Jeremy M, O’Meara, Brian C, Gilchrist, Michael A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8042768/
https://www.ncbi.nlm.nih.gov/pubmed/33306127
http://dx.doi.org/10.1093/molbev/msaa318
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author Beaulieu, Jeremy M
O’Meara, Brian C
Gilchrist, Michael A
author_facet Beaulieu, Jeremy M
O’Meara, Brian C
Gilchrist, Michael A
author_sort Beaulieu, Jeremy M
collection PubMed
description Ultraconserved elements (UCEs) are stretches of hundreds of nucleotides with highly conserved cores flanked by variable regions. Although the selective forces responsible for the preservation of UCEs are unknown, they are nonetheless believed to contain phylogenetically meaningful information from deep to shallow divergence events. Phylogenetic applications of UCEs assume the same degree of rate heterogeneity applies across the entire locus, including variable flanking regions. We present a Wright–Fisher model of selection on nucleotides (SelON) which includes the effects of mutation, drift, and spatially varying, stabilizing selection for an optimal nucleotide sequence. The SelON model assumes the strength of stabilizing selection follows a position-dependent Gaussian function whose exact shape can vary between UCEs. We evaluate SelON by comparing its performance to a simpler and spatially invariant GTR+ [Formula: see text] model using an empirical data set of 400 vertebrate UCEs used to determine the phylogenetic position of turtles. We observe much improvement in model fit of SelON over the GTR+ [Formula: see text] model, and support for turtles as sister to lepidosaurs. Overall, the UCE-specific parameters SelON estimates provide a compact way of quantifying the strength and variation in selection within and across UCEs. SelON can also be extended to include more realistic mapping functions between sequence and stabilizing selection as well as allow for greater levels of rate heterogeneity. By more explicitly modeling the nature of selection on UCEs, SelON and similar approaches can be used to better understand the biological mechanisms responsible for their preservation across highly divergent taxa and long evolutionary time scales.
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spelling pubmed-80427682021-04-16 A Spatially Explicit Model of Stabilizing Selection for Improving Phylogenetic Inference Beaulieu, Jeremy M O’Meara, Brian C Gilchrist, Michael A Mol Biol Evol Methods Ultraconserved elements (UCEs) are stretches of hundreds of nucleotides with highly conserved cores flanked by variable regions. Although the selective forces responsible for the preservation of UCEs are unknown, they are nonetheless believed to contain phylogenetically meaningful information from deep to shallow divergence events. Phylogenetic applications of UCEs assume the same degree of rate heterogeneity applies across the entire locus, including variable flanking regions. We present a Wright–Fisher model of selection on nucleotides (SelON) which includes the effects of mutation, drift, and spatially varying, stabilizing selection for an optimal nucleotide sequence. The SelON model assumes the strength of stabilizing selection follows a position-dependent Gaussian function whose exact shape can vary between UCEs. We evaluate SelON by comparing its performance to a simpler and spatially invariant GTR+ [Formula: see text] model using an empirical data set of 400 vertebrate UCEs used to determine the phylogenetic position of turtles. We observe much improvement in model fit of SelON over the GTR+ [Formula: see text] model, and support for turtles as sister to lepidosaurs. Overall, the UCE-specific parameters SelON estimates provide a compact way of quantifying the strength and variation in selection within and across UCEs. SelON can also be extended to include more realistic mapping functions between sequence and stabilizing selection as well as allow for greater levels of rate heterogeneity. By more explicitly modeling the nature of selection on UCEs, SelON and similar approaches can be used to better understand the biological mechanisms responsible for their preservation across highly divergent taxa and long evolutionary time scales. Oxford University Press 2020-12-11 /pmc/articles/PMC8042768/ /pubmed/33306127 http://dx.doi.org/10.1093/molbev/msaa318 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methods
Beaulieu, Jeremy M
O’Meara, Brian C
Gilchrist, Michael A
A Spatially Explicit Model of Stabilizing Selection for Improving Phylogenetic Inference
title A Spatially Explicit Model of Stabilizing Selection for Improving Phylogenetic Inference
title_full A Spatially Explicit Model of Stabilizing Selection for Improving Phylogenetic Inference
title_fullStr A Spatially Explicit Model of Stabilizing Selection for Improving Phylogenetic Inference
title_full_unstemmed A Spatially Explicit Model of Stabilizing Selection for Improving Phylogenetic Inference
title_short A Spatially Explicit Model of Stabilizing Selection for Improving Phylogenetic Inference
title_sort spatially explicit model of stabilizing selection for improving phylogenetic inference
topic Methods
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8042768/
https://www.ncbi.nlm.nih.gov/pubmed/33306127
http://dx.doi.org/10.1093/molbev/msaa318
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