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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
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.
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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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