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Variation of the meiotic recombination landscape and properties over a broad evolutionary distance in yeasts
Meiotic recombination is a major factor of genome evolution, deeply characterized in only a few model species, notably the yeast Saccharomyces cerevisiae. Consequently, little is known about variations of its properties across species. In this respect, we explored the recombination landscape of Lach...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5554000/ https://www.ncbi.nlm.nih.gov/pubmed/28763437 http://dx.doi.org/10.1371/journal.pgen.1006917 |
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author | Brion, Christian Legrand, Sylvain Peter, Jackson Caradec, Claudia Pflieger, David Hou, Jing Friedrich, Anne Llorente, Bertrand Schacherer, Joseph |
author_facet | Brion, Christian Legrand, Sylvain Peter, Jackson Caradec, Claudia Pflieger, David Hou, Jing Friedrich, Anne Llorente, Bertrand Schacherer, Joseph |
author_sort | Brion, Christian |
collection | PubMed |
description | Meiotic recombination is a major factor of genome evolution, deeply characterized in only a few model species, notably the yeast Saccharomyces cerevisiae. Consequently, little is known about variations of its properties across species. In this respect, we explored the recombination landscape of Lachancea kluyveri, a protoploid yeast species that diverged from the Saccharomyces genus more than 100 million years ago and we found striking differences with S. cerevisiae. These variations include a lower recombination rate, a higher frequency of chromosomes segregating without any crossover and the absence of recombination on the chromosome arm containing the sex locus. In addition, although well conserved within the Saccharomyces clade, the S. cerevisiae recombination hotspots are not conserved over a broader evolutionary distance. Finally and strikingly, we found evidence of frequent reversal of commitment to meiosis, resulting in return to mitotic growth after allele shuffling. Identification of this major but underestimated evolutionary phenomenon illustrates the relevance of exploring non-model species. |
format | Online Article Text |
id | pubmed-5554000 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-55540002017-08-25 Variation of the meiotic recombination landscape and properties over a broad evolutionary distance in yeasts Brion, Christian Legrand, Sylvain Peter, Jackson Caradec, Claudia Pflieger, David Hou, Jing Friedrich, Anne Llorente, Bertrand Schacherer, Joseph PLoS Genet Research Article Meiotic recombination is a major factor of genome evolution, deeply characterized in only a few model species, notably the yeast Saccharomyces cerevisiae. Consequently, little is known about variations of its properties across species. In this respect, we explored the recombination landscape of Lachancea kluyveri, a protoploid yeast species that diverged from the Saccharomyces genus more than 100 million years ago and we found striking differences with S. cerevisiae. These variations include a lower recombination rate, a higher frequency of chromosomes segregating without any crossover and the absence of recombination on the chromosome arm containing the sex locus. In addition, although well conserved within the Saccharomyces clade, the S. cerevisiae recombination hotspots are not conserved over a broader evolutionary distance. Finally and strikingly, we found evidence of frequent reversal of commitment to meiosis, resulting in return to mitotic growth after allele shuffling. Identification of this major but underestimated evolutionary phenomenon illustrates the relevance of exploring non-model species. Public Library of Science 2017-08-01 /pmc/articles/PMC5554000/ /pubmed/28763437 http://dx.doi.org/10.1371/journal.pgen.1006917 Text en © 2017 Brion et al http://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/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Brion, Christian Legrand, Sylvain Peter, Jackson Caradec, Claudia Pflieger, David Hou, Jing Friedrich, Anne Llorente, Bertrand Schacherer, Joseph Variation of the meiotic recombination landscape and properties over a broad evolutionary distance in yeasts |
title | Variation of the meiotic recombination landscape and properties over a broad evolutionary distance in yeasts |
title_full | Variation of the meiotic recombination landscape and properties over a broad evolutionary distance in yeasts |
title_fullStr | Variation of the meiotic recombination landscape and properties over a broad evolutionary distance in yeasts |
title_full_unstemmed | Variation of the meiotic recombination landscape and properties over a broad evolutionary distance in yeasts |
title_short | Variation of the meiotic recombination landscape and properties over a broad evolutionary distance in yeasts |
title_sort | variation of the meiotic recombination landscape and properties over a broad evolutionary distance in yeasts |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5554000/ https://www.ncbi.nlm.nih.gov/pubmed/28763437 http://dx.doi.org/10.1371/journal.pgen.1006917 |
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