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Protein innovation through template switching in the Saccharomyces cerevisiae lineage
DNA polymerase template switching between short, non-identical inverted repeats (IRs) is a genetic mechanism that leads to the homogenization of IR arms and to IR spacer inversion, which cause multinucleotide mutations (MNMs). It is unknown if and how template switching affects gene evolution. In th...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8604942/ https://www.ncbi.nlm.nih.gov/pubmed/34799587 http://dx.doi.org/10.1038/s41598-021-01736-y |
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author | Abraham, May Hazkani-Covo, Einat |
author_facet | Abraham, May Hazkani-Covo, Einat |
author_sort | Abraham, May |
collection | PubMed |
description | DNA polymerase template switching between short, non-identical inverted repeats (IRs) is a genetic mechanism that leads to the homogenization of IR arms and to IR spacer inversion, which cause multinucleotide mutations (MNMs). It is unknown if and how template switching affects gene evolution. In this study, we performed a phylogenetic analysis to determine the effect of template switching between IR arms on coding DNA of Saccharomyces cerevisiae. To achieve this, perfect IRs that co-occurred with MNMs between a strain and its parental node were identified in S. cerevisiae strains. We determined that template switching introduced MNMs into 39 protein-coding genes through S. cerevisiae evolution, resulting in both arm homogenization and inversion of the IR spacer. These events in turn resulted in nonsynonymous substitutions and up to five neighboring amino acid replacements in a single gene. The study demonstrates that template switching is a powerful generator of multiple substitutions within codons. Additionally, some template switching events occurred more than once during S. cerevisiae evolution. Our findings suggest that template switching constitutes a general mutagenic mechanism that results in both nonsynonymous substitutions and parallel evolution, which are traditionally considered as evidence for positive selection, without the need for adaptive explanations. |
format | Online Article Text |
id | pubmed-8604942 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-86049422021-11-22 Protein innovation through template switching in the Saccharomyces cerevisiae lineage Abraham, May Hazkani-Covo, Einat Sci Rep Article DNA polymerase template switching between short, non-identical inverted repeats (IRs) is a genetic mechanism that leads to the homogenization of IR arms and to IR spacer inversion, which cause multinucleotide mutations (MNMs). It is unknown if and how template switching affects gene evolution. In this study, we performed a phylogenetic analysis to determine the effect of template switching between IR arms on coding DNA of Saccharomyces cerevisiae. To achieve this, perfect IRs that co-occurred with MNMs between a strain and its parental node were identified in S. cerevisiae strains. We determined that template switching introduced MNMs into 39 protein-coding genes through S. cerevisiae evolution, resulting in both arm homogenization and inversion of the IR spacer. These events in turn resulted in nonsynonymous substitutions and up to five neighboring amino acid replacements in a single gene. The study demonstrates that template switching is a powerful generator of multiple substitutions within codons. Additionally, some template switching events occurred more than once during S. cerevisiae evolution. Our findings suggest that template switching constitutes a general mutagenic mechanism that results in both nonsynonymous substitutions and parallel evolution, which are traditionally considered as evidence for positive selection, without the need for adaptive explanations. Nature Publishing Group UK 2021-11-19 /pmc/articles/PMC8604942/ /pubmed/34799587 http://dx.doi.org/10.1038/s41598-021-01736-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Abraham, May Hazkani-Covo, Einat Protein innovation through template switching in the Saccharomyces cerevisiae lineage |
title | Protein innovation through template switching in the Saccharomyces cerevisiae lineage |
title_full | Protein innovation through template switching in the Saccharomyces cerevisiae lineage |
title_fullStr | Protein innovation through template switching in the Saccharomyces cerevisiae lineage |
title_full_unstemmed | Protein innovation through template switching in the Saccharomyces cerevisiae lineage |
title_short | Protein innovation through template switching in the Saccharomyces cerevisiae lineage |
title_sort | protein innovation through template switching in the saccharomyces cerevisiae lineage |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8604942/ https://www.ncbi.nlm.nih.gov/pubmed/34799587 http://dx.doi.org/10.1038/s41598-021-01736-y |
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