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Multinucleotide mutations cause false inferences of lineage-specific positive selection

Phylogenetic tests of adaptive evolution, such as the widely used branch-site test, assume that nucleotide substitutions occur singly and independently. But recent research has shown that errors at adjacent sites often occur during DNA replication, and the resulting multinucleotide mutations (MNMs)...

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Autores principales: Venkat, Aarti, Hahn, Matthew W., Thornton, Joseph W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6093625/
https://www.ncbi.nlm.nih.gov/pubmed/29967485
http://dx.doi.org/10.1038/s41559-018-0584-5
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author Venkat, Aarti
Hahn, Matthew W.
Thornton, Joseph W.
author_facet Venkat, Aarti
Hahn, Matthew W.
Thornton, Joseph W.
author_sort Venkat, Aarti
collection PubMed
description Phylogenetic tests of adaptive evolution, such as the widely used branch-site test, assume that nucleotide substitutions occur singly and independently. But recent research has shown that errors at adjacent sites often occur during DNA replication, and the resulting multinucleotide mutations (MNMs) are overwhelmingly likely to be nonsynonymous. We evaluated whether the branch-site test (BST) might misinterpret sequence patterns produced by MNMs as false support for positive selection. We analyzed two genome-scale datasets– one from mammals and one from flies – and found that codons with multiple differences account for virtually all the support for lineage-specific positive selection in the BST. Simulations under conditions derived from these alignments but without positive selection show that realistic rates of MNMs cause a strong and systematic bias towards false inferences of selection. This bias is sufficient under empirically derived conditions to produce false positive inferences as often as the branch-site test infers positive selection from the empirical data. Although some genes with BST-positive results may have evolved adaptively, the test cannot distinguish sequence patterns produced by authentic positive selection from those caused by neutral fixation of MNMs. Many published inferences of adaptive evolution using this technique may therefore be artifacts of model violation caused by unincorporated neutral mutational processes. We introduce a model that incorporates MNMs and may help to ameliorate this bias.
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spelling pubmed-60936252019-01-02 Multinucleotide mutations cause false inferences of lineage-specific positive selection Venkat, Aarti Hahn, Matthew W. Thornton, Joseph W. Nat Ecol Evol Article Phylogenetic tests of adaptive evolution, such as the widely used branch-site test, assume that nucleotide substitutions occur singly and independently. But recent research has shown that errors at adjacent sites often occur during DNA replication, and the resulting multinucleotide mutations (MNMs) are overwhelmingly likely to be nonsynonymous. We evaluated whether the branch-site test (BST) might misinterpret sequence patterns produced by MNMs as false support for positive selection. We analyzed two genome-scale datasets– one from mammals and one from flies – and found that codons with multiple differences account for virtually all the support for lineage-specific positive selection in the BST. Simulations under conditions derived from these alignments but without positive selection show that realistic rates of MNMs cause a strong and systematic bias towards false inferences of selection. This bias is sufficient under empirically derived conditions to produce false positive inferences as often as the branch-site test infers positive selection from the empirical data. Although some genes with BST-positive results may have evolved adaptively, the test cannot distinguish sequence patterns produced by authentic positive selection from those caused by neutral fixation of MNMs. Many published inferences of adaptive evolution using this technique may therefore be artifacts of model violation caused by unincorporated neutral mutational processes. We introduce a model that incorporates MNMs and may help to ameliorate this bias. 2018-07-02 2018-08 /pmc/articles/PMC6093625/ /pubmed/29967485 http://dx.doi.org/10.1038/s41559-018-0584-5 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Venkat, Aarti
Hahn, Matthew W.
Thornton, Joseph W.
Multinucleotide mutations cause false inferences of lineage-specific positive selection
title Multinucleotide mutations cause false inferences of lineage-specific positive selection
title_full Multinucleotide mutations cause false inferences of lineage-specific positive selection
title_fullStr Multinucleotide mutations cause false inferences of lineage-specific positive selection
title_full_unstemmed Multinucleotide mutations cause false inferences of lineage-specific positive selection
title_short Multinucleotide mutations cause false inferences of lineage-specific positive selection
title_sort multinucleotide mutations cause false inferences of lineage-specific positive selection
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6093625/
https://www.ncbi.nlm.nih.gov/pubmed/29967485
http://dx.doi.org/10.1038/s41559-018-0584-5
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