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Mitogenomics and mitochondrial gene phylogeny decipher the evolution of Saccharomycotina yeasts
Saccharomycotina yeasts belong to diverse clades within the kingdom of fungi and are important to human everyday life. This work investigates the evolutionary relationships among these yeasts from a mitochondrial (mt) genomic perspective. A comparative study of 155 yeast mt genomes representing all...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9154068/ https://www.ncbi.nlm.nih.gov/pubmed/35576568 http://dx.doi.org/10.1093/gbe/evac073 |
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author | Christinaki, Anastasia C. Kanellopoulos, Spyros G. Kortsinoglou, Alexandra M. Andrikopoulos, Marios Α. Theelen, Bart Boekhout, Teun Kouvelis, Vassili N. |
author_facet | Christinaki, Anastasia C. Kanellopoulos, Spyros G. Kortsinoglou, Alexandra M. Andrikopoulos, Marios Α. Theelen, Bart Boekhout, Teun Kouvelis, Vassili N. |
author_sort | Christinaki, Anastasia C. |
collection | PubMed |
description | Saccharomycotina yeasts belong to diverse clades within the kingdom of fungi and are important to human everyday life. This work investigates the evolutionary relationships among these yeasts from a mitochondrial (mt) genomic perspective. A comparative study of 155 yeast mt genomes representing all major phylogenetic lineages of Saccharomycotina was performed, including genome size and content variability, intron and intergenic regions’ diversity, genetic code alterations, and syntenic variation. Findings from this study suggest that mt genome size diversity is the result of a ceaseless random process, mainly based on genetic recombination and intron mobility. Gene order analysis revealed conserved syntenic units and many occurring rearrangements, which can be correlated with major evolutionary events as shown by the phylogenetic analysis of the concatenated mt protein matrix. For the first time, molecular dating indicated a slower mt genome divergence rate in the early stages of yeast evolution, in contrast with a faster rate in the late evolutionary stages, compared to their nuclear time divergence. Genetic code reassignments of mt genomes are a perpetual process happening in many different parallel evolutionary steps throughout the evolution of Saccharomycotina. Overall, this work shows that phylogenetic studies based on the mt genome of yeasts highlight major evolutionary events. |
format | Online Article Text |
id | pubmed-9154068 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-91540682022-06-04 Mitogenomics and mitochondrial gene phylogeny decipher the evolution of Saccharomycotina yeasts Christinaki, Anastasia C. Kanellopoulos, Spyros G. Kortsinoglou, Alexandra M. Andrikopoulos, Marios Α. Theelen, Bart Boekhout, Teun Kouvelis, Vassili N. Genome Biol Evol Research Article Saccharomycotina yeasts belong to diverse clades within the kingdom of fungi and are important to human everyday life. This work investigates the evolutionary relationships among these yeasts from a mitochondrial (mt) genomic perspective. A comparative study of 155 yeast mt genomes representing all major phylogenetic lineages of Saccharomycotina was performed, including genome size and content variability, intron and intergenic regions’ diversity, genetic code alterations, and syntenic variation. Findings from this study suggest that mt genome size diversity is the result of a ceaseless random process, mainly based on genetic recombination and intron mobility. Gene order analysis revealed conserved syntenic units and many occurring rearrangements, which can be correlated with major evolutionary events as shown by the phylogenetic analysis of the concatenated mt protein matrix. For the first time, molecular dating indicated a slower mt genome divergence rate in the early stages of yeast evolution, in contrast with a faster rate in the late evolutionary stages, compared to their nuclear time divergence. Genetic code reassignments of mt genomes are a perpetual process happening in many different parallel evolutionary steps throughout the evolution of Saccharomycotina. Overall, this work shows that phylogenetic studies based on the mt genome of yeasts highlight major evolutionary events. Oxford University Press 2022-05-16 /pmc/articles/PMC9154068/ /pubmed/35576568 http://dx.doi.org/10.1093/gbe/evac073 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Research Article Christinaki, Anastasia C. Kanellopoulos, Spyros G. Kortsinoglou, Alexandra M. Andrikopoulos, Marios Α. Theelen, Bart Boekhout, Teun Kouvelis, Vassili N. Mitogenomics and mitochondrial gene phylogeny decipher the evolution of Saccharomycotina yeasts |
title | Mitogenomics and mitochondrial gene phylogeny decipher the evolution of Saccharomycotina yeasts |
title_full | Mitogenomics and mitochondrial gene phylogeny decipher the evolution of Saccharomycotina yeasts |
title_fullStr | Mitogenomics and mitochondrial gene phylogeny decipher the evolution of Saccharomycotina yeasts |
title_full_unstemmed | Mitogenomics and mitochondrial gene phylogeny decipher the evolution of Saccharomycotina yeasts |
title_short | Mitogenomics and mitochondrial gene phylogeny decipher the evolution of Saccharomycotina yeasts |
title_sort | mitogenomics and mitochondrial gene phylogeny decipher the evolution of saccharomycotina yeasts |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9154068/ https://www.ncbi.nlm.nih.gov/pubmed/35576568 http://dx.doi.org/10.1093/gbe/evac073 |
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