Cargando…

Crossing fitness valleys via double substitutions within codons

BACKGROUND: Single nucleotide substitutions in protein-coding genes can be divided into synonymous (S), with little fitness effect, and non-synonymous (N) ones that alter amino acids and thus generally have a greater effect. Most of the N substitutions are affected by purifying selection that elimin...

Descripción completa

Detalles Bibliográficos
Autores principales: Belinky, Frida, Sela, Itamar, Rogozin, Igor B., Koonin, Eugene V.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6916188/
https://www.ncbi.nlm.nih.gov/pubmed/31842858
http://dx.doi.org/10.1186/s12915-019-0727-4
_version_ 1783480180321288192
author Belinky, Frida
Sela, Itamar
Rogozin, Igor B.
Koonin, Eugene V.
author_facet Belinky, Frida
Sela, Itamar
Rogozin, Igor B.
Koonin, Eugene V.
author_sort Belinky, Frida
collection PubMed
description BACKGROUND: Single nucleotide substitutions in protein-coding genes can be divided into synonymous (S), with little fitness effect, and non-synonymous (N) ones that alter amino acids and thus generally have a greater effect. Most of the N substitutions are affected by purifying selection that eliminates them from evolving populations. However, additional mutations of nearby bases potentially could alleviate the deleterious effect of single substitutions, making them subject to positive selection. To elucidate the effects of selection on double substitutions in all codons, it is critical to differentiate selection from mutational biases. RESULTS: We addressed the evolutionary regimes of within-codon double substitutions in 37 groups of closely related prokaryotic genomes from diverse phyla by comparing the fractions of double substitutions within codons to those of the equivalent double S substitutions in adjacent codons. Under the assumption that substitutions occur one at a time, all within-codon double substitutions can be represented as “ancestral-intermediate-final” sequences (where “intermediate” refers to the first single substitution and “final” refers to the second substitution) and can be partitioned into four classes: (1) SS, S intermediate–S final; (2) SN, S intermediate–N final; (3) NS, N intermediate–S final; and (4) NN, N intermediate–N final. We found that the selective pressure on the second substitution markedly differs among these classes of double substitutions. Analogous to single S (synonymous) substitutions, SS double substitutions evolve neutrally, whereas analogous to single N (non-synonymous) substitutions, SN double substitutions are subject to purifying selection. In contrast, NS show positive selection on the second step because the original amino acid is recovered. The NN double substitutions are heterogeneous and can be subject to either purifying or positive selection, or evolve neutrally, depending on the amino acid similarity between the final or intermediate and the ancestral states. CONCLUSIONS: The results of the present, comprehensive analysis of the evolutionary landscape of within-codon double substitutions reaffirm the largely conservative regime of protein evolution. However, the second step of a double substitution can be subject to positive selection when the first step is deleterious. Such positive selection can result in frequent crossing of valleys on the fitness landscape.
format Online
Article
Text
id pubmed-6916188
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-69161882019-12-30 Crossing fitness valleys via double substitutions within codons Belinky, Frida Sela, Itamar Rogozin, Igor B. Koonin, Eugene V. BMC Biol Research Article BACKGROUND: Single nucleotide substitutions in protein-coding genes can be divided into synonymous (S), with little fitness effect, and non-synonymous (N) ones that alter amino acids and thus generally have a greater effect. Most of the N substitutions are affected by purifying selection that eliminates them from evolving populations. However, additional mutations of nearby bases potentially could alleviate the deleterious effect of single substitutions, making them subject to positive selection. To elucidate the effects of selection on double substitutions in all codons, it is critical to differentiate selection from mutational biases. RESULTS: We addressed the evolutionary regimes of within-codon double substitutions in 37 groups of closely related prokaryotic genomes from diverse phyla by comparing the fractions of double substitutions within codons to those of the equivalent double S substitutions in adjacent codons. Under the assumption that substitutions occur one at a time, all within-codon double substitutions can be represented as “ancestral-intermediate-final” sequences (where “intermediate” refers to the first single substitution and “final” refers to the second substitution) and can be partitioned into four classes: (1) SS, S intermediate–S final; (2) SN, S intermediate–N final; (3) NS, N intermediate–S final; and (4) NN, N intermediate–N final. We found that the selective pressure on the second substitution markedly differs among these classes of double substitutions. Analogous to single S (synonymous) substitutions, SS double substitutions evolve neutrally, whereas analogous to single N (non-synonymous) substitutions, SN double substitutions are subject to purifying selection. In contrast, NS show positive selection on the second step because the original amino acid is recovered. The NN double substitutions are heterogeneous and can be subject to either purifying or positive selection, or evolve neutrally, depending on the amino acid similarity between the final or intermediate and the ancestral states. CONCLUSIONS: The results of the present, comprehensive analysis of the evolutionary landscape of within-codon double substitutions reaffirm the largely conservative regime of protein evolution. However, the second step of a double substitution can be subject to positive selection when the first step is deleterious. Such positive selection can result in frequent crossing of valleys on the fitness landscape. BioMed Central 2019-12-16 /pmc/articles/PMC6916188/ /pubmed/31842858 http://dx.doi.org/10.1186/s12915-019-0727-4 Text en © The Author(s). 2019 Open AccessThis 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 Research Article
Belinky, Frida
Sela, Itamar
Rogozin, Igor B.
Koonin, Eugene V.
Crossing fitness valleys via double substitutions within codons
title Crossing fitness valleys via double substitutions within codons
title_full Crossing fitness valleys via double substitutions within codons
title_fullStr Crossing fitness valleys via double substitutions within codons
title_full_unstemmed Crossing fitness valleys via double substitutions within codons
title_short Crossing fitness valleys via double substitutions within codons
title_sort crossing fitness valleys via double substitutions within codons
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6916188/
https://www.ncbi.nlm.nih.gov/pubmed/31842858
http://dx.doi.org/10.1186/s12915-019-0727-4
work_keys_str_mv AT belinkyfrida crossingfitnessvalleysviadoublesubstitutionswithincodons
AT selaitamar crossingfitnessvalleysviadoublesubstitutionswithincodons
AT rogozinigorb crossingfitnessvalleysviadoublesubstitutionswithincodons
AT koonineugenev crossingfitnessvalleysviadoublesubstitutionswithincodons