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Contrasting evolutionary genome dynamics between domesticated and wild yeasts
Structural rearrangements have long been recognized as an important source of genetic variation with implications in phenotypic diversity and disease, yet their detailed evolutionary dynamics remain elusive. Here, we use long-read sequencing to generate end-to-end genome assemblies for 12 strains re...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5446901/ https://www.ncbi.nlm.nih.gov/pubmed/28416820 http://dx.doi.org/10.1038/ng.3847 |
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author | Yue, Jia-Xing Li, Jing Aigrain, Louise Hallin, Johan Persson, Karl Oliver, Karen Bergström, Anders Coupland, Paul Warringer, Jonas Lagomarsino, Marco Consentino Fischer, Gilles Durbin, Richard Liti, Gianni |
author_facet | Yue, Jia-Xing Li, Jing Aigrain, Louise Hallin, Johan Persson, Karl Oliver, Karen Bergström, Anders Coupland, Paul Warringer, Jonas Lagomarsino, Marco Consentino Fischer, Gilles Durbin, Richard Liti, Gianni |
author_sort | Yue, Jia-Xing |
collection | PubMed |
description | Structural rearrangements have long been recognized as an important source of genetic variation with implications in phenotypic diversity and disease, yet their detailed evolutionary dynamics remain elusive. Here, we use long-read sequencing to generate end-to-end genome assemblies for 12 strains representing major subpopulations of the partially domesticated yeast Saccharomyces cerevisiae and its wild relative Saccharomyces paradoxus. These population-level high-quality genomes with comprehensive annotation allow for the first time a precise definition of chromosomal boundaries between cores and subtelomeres and a high-resolution view of evolutionary genome dynamics. In chromosomal cores, S. paradoxus exhibits faster accumulation of balanced rearrangements (inversions, reciprocal translocations and transpositions) whereas S. cerevisiae accumulates unbalanced rearrangements (novel insertions, deletions and duplications) more rapidly. In subtelomeres, both species show extensive interchromosomal reshuffling, with a higher tempo in S. cerevisiae. Such striking contrasts between wild and domesticated yeasts likely reflect the influence of human activities on structural genome evolution. |
format | Online Article Text |
id | pubmed-5446901 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
record_format | MEDLINE/PubMed |
spelling | pubmed-54469012017-10-17 Contrasting evolutionary genome dynamics between domesticated and wild yeasts Yue, Jia-Xing Li, Jing Aigrain, Louise Hallin, Johan Persson, Karl Oliver, Karen Bergström, Anders Coupland, Paul Warringer, Jonas Lagomarsino, Marco Consentino Fischer, Gilles Durbin, Richard Liti, Gianni Nat Genet Article Structural rearrangements have long been recognized as an important source of genetic variation with implications in phenotypic diversity and disease, yet their detailed evolutionary dynamics remain elusive. Here, we use long-read sequencing to generate end-to-end genome assemblies for 12 strains representing major subpopulations of the partially domesticated yeast Saccharomyces cerevisiae and its wild relative Saccharomyces paradoxus. These population-level high-quality genomes with comprehensive annotation allow for the first time a precise definition of chromosomal boundaries between cores and subtelomeres and a high-resolution view of evolutionary genome dynamics. In chromosomal cores, S. paradoxus exhibits faster accumulation of balanced rearrangements (inversions, reciprocal translocations and transpositions) whereas S. cerevisiae accumulates unbalanced rearrangements (novel insertions, deletions and duplications) more rapidly. In subtelomeres, both species show extensive interchromosomal reshuffling, with a higher tempo in S. cerevisiae. Such striking contrasts between wild and domesticated yeasts likely reflect the influence of human activities on structural genome evolution. 2017-04-17 2017-06 /pmc/articles/PMC5446901/ /pubmed/28416820 http://dx.doi.org/10.1038/ng.3847 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Yue, Jia-Xing Li, Jing Aigrain, Louise Hallin, Johan Persson, Karl Oliver, Karen Bergström, Anders Coupland, Paul Warringer, Jonas Lagomarsino, Marco Consentino Fischer, Gilles Durbin, Richard Liti, Gianni Contrasting evolutionary genome dynamics between domesticated and wild yeasts |
title | Contrasting evolutionary genome dynamics between domesticated and wild yeasts |
title_full | Contrasting evolutionary genome dynamics between domesticated and wild yeasts |
title_fullStr | Contrasting evolutionary genome dynamics between domesticated and wild yeasts |
title_full_unstemmed | Contrasting evolutionary genome dynamics between domesticated and wild yeasts |
title_short | Contrasting evolutionary genome dynamics between domesticated and wild yeasts |
title_sort | contrasting evolutionary genome dynamics between domesticated and wild yeasts |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5446901/ https://www.ncbi.nlm.nih.gov/pubmed/28416820 http://dx.doi.org/10.1038/ng.3847 |
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