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Evolution of intraspecific transcriptomic landscapes in yeasts

Variations in gene expression have been widely explored in order to obtain an accurate overview of the changes in regulatory networks that underlie phenotypic diversity. Numerous studies have characterized differences in genomic expression between large numbers of individuals of model organisms such...

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Autores principales: Brion, Christian, Pflieger, David, Friedrich, Anne, 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/PMC4482089/
https://www.ncbi.nlm.nih.gov/pubmed/25897111
http://dx.doi.org/10.1093/nar/gkv363
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author Brion, Christian
Pflieger, David
Friedrich, Anne
Schacherer, Joseph
author_facet Brion, Christian
Pflieger, David
Friedrich, Anne
Schacherer, Joseph
author_sort Brion, Christian
collection PubMed
description Variations in gene expression have been widely explored in order to obtain an accurate overview of the changes in regulatory networks that underlie phenotypic diversity. Numerous studies have characterized differences in genomic expression between large numbers of individuals of model organisms such as Saccharomyces cerevisiae. To more broadly survey the evolution of the transcriptomic landscape across species, we measured whole-genome expression in a large collection of another yeast species: Lachancea kluyveri (formerly Saccharomyces kluyveri), using RNAseq. Interestingly, this species diverged from the S. cerevisiae lineage prior to its ancestral whole genome duplication. Moreover, L. kluyveri harbors a chromosome-scale compositional heterogeneity due to a 1-Mb ancestral introgressed region as well as a large set of unique unannotated genes. In this context, our comparative transcriptomic analysis clearly showed a link between gene evolutionary history and expression behavior. Indeed, genes that have been recently acquired or under function relaxation tend to be less transcribed show a higher intraspecific variation (plasticity) and are less involved in network (connectivity). Moreover, utilizing this approach in L. kluyveri also highlighted specific regulatory network signatures in aerobic respiration, amino-acid biosynthesis and glycosylation, presumably due to its different lifestyle. Our data set sheds an important light on the evolution of intraspecific transcriptomic variation across distant species.
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spelling pubmed-44820892015-06-30 Evolution of intraspecific transcriptomic landscapes in yeasts Brion, Christian Pflieger, David Friedrich, Anne Schacherer, Joseph Nucleic Acids Res Genomics Variations in gene expression have been widely explored in order to obtain an accurate overview of the changes in regulatory networks that underlie phenotypic diversity. Numerous studies have characterized differences in genomic expression between large numbers of individuals of model organisms such as Saccharomyces cerevisiae. To more broadly survey the evolution of the transcriptomic landscape across species, we measured whole-genome expression in a large collection of another yeast species: Lachancea kluyveri (formerly Saccharomyces kluyveri), using RNAseq. Interestingly, this species diverged from the S. cerevisiae lineage prior to its ancestral whole genome duplication. Moreover, L. kluyveri harbors a chromosome-scale compositional heterogeneity due to a 1-Mb ancestral introgressed region as well as a large set of unique unannotated genes. In this context, our comparative transcriptomic analysis clearly showed a link between gene evolutionary history and expression behavior. Indeed, genes that have been recently acquired or under function relaxation tend to be less transcribed show a higher intraspecific variation (plasticity) and are less involved in network (connectivity). Moreover, utilizing this approach in L. kluyveri also highlighted specific regulatory network signatures in aerobic respiration, amino-acid biosynthesis and glycosylation, presumably due to its different lifestyle. Our data set sheds an important light on the evolution of intraspecific transcriptomic variation across distant species. Oxford University Press 2015-05-19 2015-04-20 /pmc/articles/PMC4482089/ /pubmed/25897111 http://dx.doi.org/10.1093/nar/gkv363 Text en © The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Genomics
Brion, Christian
Pflieger, David
Friedrich, Anne
Schacherer, Joseph
Evolution of intraspecific transcriptomic landscapes in yeasts
title Evolution of intraspecific transcriptomic landscapes in yeasts
title_full Evolution of intraspecific transcriptomic landscapes in yeasts
title_fullStr Evolution of intraspecific transcriptomic landscapes in yeasts
title_full_unstemmed Evolution of intraspecific transcriptomic landscapes in yeasts
title_short Evolution of intraspecific transcriptomic landscapes in yeasts
title_sort evolution of intraspecific transcriptomic landscapes in yeasts
topic Genomics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4482089/
https://www.ncbi.nlm.nih.gov/pubmed/25897111
http://dx.doi.org/10.1093/nar/gkv363
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