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Rapid functional and evolutionary changes follow gene duplication in yeast

Duplication of genes or genomes provides the raw material for evolutionary innovation. After duplication a gene may be lost, recombine with another gene, have its function modified or be retained in an unaltered state. The fate of duplication is usually studied by comparing extant genomes and recons...

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Autores principales: Naseeb, Samina, Ames, Ryan M., Delneri, Daniela, Lovell, Simon C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5577496/
https://www.ncbi.nlm.nih.gov/pubmed/28835561
http://dx.doi.org/10.1098/rspb.2017.1393
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author Naseeb, Samina
Ames, Ryan M.
Delneri, Daniela
Lovell, Simon C.
author_facet Naseeb, Samina
Ames, Ryan M.
Delneri, Daniela
Lovell, Simon C.
author_sort Naseeb, Samina
collection PubMed
description Duplication of genes or genomes provides the raw material for evolutionary innovation. After duplication a gene may be lost, recombine with another gene, have its function modified or be retained in an unaltered state. The fate of duplication is usually studied by comparing extant genomes and reconstructing the most likely ancestral states. Valuable as this approach is, it may miss the most rapid evolutionary events. Here, we engineered strains of Saccharomyces cerevisiae carrying tandem and non-tandem duplications of the singleton gene IFA38 to monitor (i) the fate of the duplicates in different conditions, including time scale and asymmetry of gene loss, and (ii) the changes in fitness and transcriptome of the strains immediately after duplication and after experimental evolution. We found that the duplication brings widespread transcriptional changes, but a fitness advantage is only present in fermentable media. In respiratory conditions, the yeast strains consistently lose the non-tandem IFA38 gene copy in a surprisingly short time, within only a few generations. This gene loss appears to be asymmetric and dependent on genome location, since the original IFA38 copy and the tandem duplicate are retained. Overall, this work shows for the first time that gene loss can be extremely rapid and context dependent.
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spelling pubmed-55774962017-08-31 Rapid functional and evolutionary changes follow gene duplication in yeast Naseeb, Samina Ames, Ryan M. Delneri, Daniela Lovell, Simon C. Proc Biol Sci Evolution Duplication of genes or genomes provides the raw material for evolutionary innovation. After duplication a gene may be lost, recombine with another gene, have its function modified or be retained in an unaltered state. The fate of duplication is usually studied by comparing extant genomes and reconstructing the most likely ancestral states. Valuable as this approach is, it may miss the most rapid evolutionary events. Here, we engineered strains of Saccharomyces cerevisiae carrying tandem and non-tandem duplications of the singleton gene IFA38 to monitor (i) the fate of the duplicates in different conditions, including time scale and asymmetry of gene loss, and (ii) the changes in fitness and transcriptome of the strains immediately after duplication and after experimental evolution. We found that the duplication brings widespread transcriptional changes, but a fitness advantage is only present in fermentable media. In respiratory conditions, the yeast strains consistently lose the non-tandem IFA38 gene copy in a surprisingly short time, within only a few generations. This gene loss appears to be asymmetric and dependent on genome location, since the original IFA38 copy and the tandem duplicate are retained. Overall, this work shows for the first time that gene loss can be extremely rapid and context dependent. The Royal Society 2017-08-30 2017-08-23 /pmc/articles/PMC5577496/ /pubmed/28835561 http://dx.doi.org/10.1098/rspb.2017.1393 Text en © 2017 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Evolution
Naseeb, Samina
Ames, Ryan M.
Delneri, Daniela
Lovell, Simon C.
Rapid functional and evolutionary changes follow gene duplication in yeast
title Rapid functional and evolutionary changes follow gene duplication in yeast
title_full Rapid functional and evolutionary changes follow gene duplication in yeast
title_fullStr Rapid functional and evolutionary changes follow gene duplication in yeast
title_full_unstemmed Rapid functional and evolutionary changes follow gene duplication in yeast
title_short Rapid functional and evolutionary changes follow gene duplication in yeast
title_sort rapid functional and evolutionary changes follow gene duplication in yeast
topic Evolution
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5577496/
https://www.ncbi.nlm.nih.gov/pubmed/28835561
http://dx.doi.org/10.1098/rspb.2017.1393
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