Cargando…

Population Genomics Reveals Chromosome-Scale Heterogeneous Evolution in a Protoploid Yeast

Yeast species represent an ideal model system for population genomic studies but large-scale polymorphism surveys have only been reported for species of the Saccharomyces genus so far. Hence, little is known about intraspecific diversity and evolution in yeast. To obtain a new insight into the evolu...

Descripción completa

Detalles Bibliográficos
Autores principales: Friedrich, Anne, Jung, Paul, Reisser, Cyrielle, Fischer, Gilles, Schacherer, Joseph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4271529/
https://www.ncbi.nlm.nih.gov/pubmed/25349286
http://dx.doi.org/10.1093/molbev/msu295
_version_ 1782349623047749632
author Friedrich, Anne
Jung, Paul
Reisser, Cyrielle
Fischer, Gilles
Schacherer, Joseph
author_facet Friedrich, Anne
Jung, Paul
Reisser, Cyrielle
Fischer, Gilles
Schacherer, Joseph
author_sort Friedrich, Anne
collection PubMed
description Yeast species represent an ideal model system for population genomic studies but large-scale polymorphism surveys have only been reported for species of the Saccharomyces genus so far. Hence, little is known about intraspecific diversity and evolution in yeast. To obtain a new insight into the evolutionary forces shaping natural populations, we sequenced the genomes of an expansive worldwide collection of isolates from a species distantly related to Saccharomyces cerevisiae: Lachancea kluyveri (formerly S. kluyveri). We identified 6.5 million single nucleotide polymorphisms and showed that a large introgression event of 1 Mb of GC-rich sequence in the chromosomal arm probably occurred in the last common ancestor of all L. kluyveri strains. Our population genomic data clearly revealed that this 1-Mb region underwent a molecular evolution pattern very different from the rest of the genome. It is characterized by a higher recombination rate, with a dramatically elevated A:T → G:C substitution rate, which is the signature of an increased GC-biased gene conversion. In addition, the predicted base composition at equilibrium demonstrates that the chromosome-scale compositional heterogeneity will persist after the genome has reached mutational equilibrium. Altogether, the data presented herein clearly show that distinct recombination and substitution regimes can coexist and lead to different evolutionary patterns within a single genome.
format Online
Article
Text
id pubmed-4271529
institution National Center for Biotechnology Information
language English
publishDate 2015
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-42715292015-01-13 Population Genomics Reveals Chromosome-Scale Heterogeneous Evolution in a Protoploid Yeast Friedrich, Anne Jung, Paul Reisser, Cyrielle Fischer, Gilles Schacherer, Joseph Mol Biol Evol Discoveries Yeast species represent an ideal model system for population genomic studies but large-scale polymorphism surveys have only been reported for species of the Saccharomyces genus so far. Hence, little is known about intraspecific diversity and evolution in yeast. To obtain a new insight into the evolutionary forces shaping natural populations, we sequenced the genomes of an expansive worldwide collection of isolates from a species distantly related to Saccharomyces cerevisiae: Lachancea kluyveri (formerly S. kluyveri). We identified 6.5 million single nucleotide polymorphisms and showed that a large introgression event of 1 Mb of GC-rich sequence in the chromosomal arm probably occurred in the last common ancestor of all L. kluyveri strains. Our population genomic data clearly revealed that this 1-Mb region underwent a molecular evolution pattern very different from the rest of the genome. It is characterized by a higher recombination rate, with a dramatically elevated A:T → G:C substitution rate, which is the signature of an increased GC-biased gene conversion. In addition, the predicted base composition at equilibrium demonstrates that the chromosome-scale compositional heterogeneity will persist after the genome has reached mutational equilibrium. Altogether, the data presented herein clearly show that distinct recombination and substitution regimes can coexist and lead to different evolutionary patterns within a single genome. Oxford University Press 2015-01 2014-11-27 /pmc/articles/PMC4271529/ /pubmed/25349286 http://dx.doi.org/10.1093/molbev/msu295 Text en © The Author 2014. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://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 Discoveries
Friedrich, Anne
Jung, Paul
Reisser, Cyrielle
Fischer, Gilles
Schacherer, Joseph
Population Genomics Reveals Chromosome-Scale Heterogeneous Evolution in a Protoploid Yeast
title Population Genomics Reveals Chromosome-Scale Heterogeneous Evolution in a Protoploid Yeast
title_full Population Genomics Reveals Chromosome-Scale Heterogeneous Evolution in a Protoploid Yeast
title_fullStr Population Genomics Reveals Chromosome-Scale Heterogeneous Evolution in a Protoploid Yeast
title_full_unstemmed Population Genomics Reveals Chromosome-Scale Heterogeneous Evolution in a Protoploid Yeast
title_short Population Genomics Reveals Chromosome-Scale Heterogeneous Evolution in a Protoploid Yeast
title_sort population genomics reveals chromosome-scale heterogeneous evolution in a protoploid yeast
topic Discoveries
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4271529/
https://www.ncbi.nlm.nih.gov/pubmed/25349286
http://dx.doi.org/10.1093/molbev/msu295
work_keys_str_mv AT friedrichanne populationgenomicsrevealschromosomescaleheterogeneousevolutioninaprotoploidyeast
AT jungpaul populationgenomicsrevealschromosomescaleheterogeneousevolutioninaprotoploidyeast
AT reissercyrielle populationgenomicsrevealschromosomescaleheterogeneousevolutioninaprotoploidyeast
AT fischergilles populationgenomicsrevealschromosomescaleheterogeneousevolutioninaprotoploidyeast
AT schachererjoseph populationgenomicsrevealschromosomescaleheterogeneousevolutioninaprotoploidyeast