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Genetic interactions reveal the evolutionary trajectories of duplicate genes

The characterization of functional redundancy and divergence between duplicate genes is an important step in understanding the evolution of genetic systems. Large-scale genetic network analysis in Saccharomyces cerevisiae provides a powerful perspective for addressing these questions through quantit...

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Autores principales: VanderSluis, Benjamin, Bellay, Jeremy, Musso, Gabriel, Costanzo, Michael, Papp, Balázs, Vizeacoumar, Franco J, Baryshnikova, Anastasia, Andrews, Brenda, Boone, Charles, Myers, Chad L
Formato: Texto
Lenguaje:English
Publicado: European Molecular Biology Organization 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3010121/
https://www.ncbi.nlm.nih.gov/pubmed/21081923
http://dx.doi.org/10.1038/msb.2010.82
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author VanderSluis, Benjamin
Bellay, Jeremy
Musso, Gabriel
Costanzo, Michael
Papp, Balázs
Vizeacoumar, Franco J
Baryshnikova, Anastasia
Andrews, Brenda
Boone, Charles
Myers, Chad L
author_facet VanderSluis, Benjamin
Bellay, Jeremy
Musso, Gabriel
Costanzo, Michael
Papp, Balázs
Vizeacoumar, Franco J
Baryshnikova, Anastasia
Andrews, Brenda
Boone, Charles
Myers, Chad L
author_sort VanderSluis, Benjamin
collection PubMed
description The characterization of functional redundancy and divergence between duplicate genes is an important step in understanding the evolution of genetic systems. Large-scale genetic network analysis in Saccharomyces cerevisiae provides a powerful perspective for addressing these questions through quantitative measurements of genetic interactions between pairs of duplicated genes, and more generally, through the study of genome-wide genetic interaction profiles associated with duplicated genes. We show that duplicate genes exhibit fewer genetic interactions than other genes because they tend to buffer one another functionally, whereas observed interactions are non-overlapping and reflect their divergent roles. We also show that duplicate gene pairs are highly imbalanced in their number of genetic interactions with other genes, a pattern that appears to result from asymmetric evolution, such that one duplicate evolves or degrades faster than the other and often becomes functionally or conditionally specialized. The differences in genetic interactions are predictive of differences in several other evolutionary and physiological properties of duplicate pairs.
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spelling pubmed-30101212010-12-27 Genetic interactions reveal the evolutionary trajectories of duplicate genes VanderSluis, Benjamin Bellay, Jeremy Musso, Gabriel Costanzo, Michael Papp, Balázs Vizeacoumar, Franco J Baryshnikova, Anastasia Andrews, Brenda Boone, Charles Myers, Chad L Mol Syst Biol Article The characterization of functional redundancy and divergence between duplicate genes is an important step in understanding the evolution of genetic systems. Large-scale genetic network analysis in Saccharomyces cerevisiae provides a powerful perspective for addressing these questions through quantitative measurements of genetic interactions between pairs of duplicated genes, and more generally, through the study of genome-wide genetic interaction profiles associated with duplicated genes. We show that duplicate genes exhibit fewer genetic interactions than other genes because they tend to buffer one another functionally, whereas observed interactions are non-overlapping and reflect their divergent roles. We also show that duplicate gene pairs are highly imbalanced in their number of genetic interactions with other genes, a pattern that appears to result from asymmetric evolution, such that one duplicate evolves or degrades faster than the other and often becomes functionally or conditionally specialized. The differences in genetic interactions are predictive of differences in several other evolutionary and physiological properties of duplicate pairs. European Molecular Biology Organization 2010-11-16 /pmc/articles/PMC3010121/ /pubmed/21081923 http://dx.doi.org/10.1038/msb.2010.82 Text en Copyright © 2010, EMBO and Macmillan Publishers Limited https://creativecommons.org/licenses/by-nc-sa/3.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Noncommercial Share Alike 3.0 Unported License, which allows readers to alter, transform, or build upon the article and then distribute the resulting work under the same or similar license to this one. The work must be attributed back to the original author and commercial use is not permitted without specific permission.
spellingShingle Article
VanderSluis, Benjamin
Bellay, Jeremy
Musso, Gabriel
Costanzo, Michael
Papp, Balázs
Vizeacoumar, Franco J
Baryshnikova, Anastasia
Andrews, Brenda
Boone, Charles
Myers, Chad L
Genetic interactions reveal the evolutionary trajectories of duplicate genes
title Genetic interactions reveal the evolutionary trajectories of duplicate genes
title_full Genetic interactions reveal the evolutionary trajectories of duplicate genes
title_fullStr Genetic interactions reveal the evolutionary trajectories of duplicate genes
title_full_unstemmed Genetic interactions reveal the evolutionary trajectories of duplicate genes
title_short Genetic interactions reveal the evolutionary trajectories of duplicate genes
title_sort genetic interactions reveal the evolutionary trajectories of duplicate genes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3010121/
https://www.ncbi.nlm.nih.gov/pubmed/21081923
http://dx.doi.org/10.1038/msb.2010.82
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