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Evolutionary principles of modular gene regulation in yeasts

Divergence in gene regulation can play a major role in evolution. Here, we used a phylogenetic framework to measure mRNA profiles in 15 yeast species from the phylum Ascomycota and reconstruct the evolution of their modular regulatory programs along a time course of growth on glucose over 300 millio...

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Autores principales: Thompson, Dawn A, Roy, Sushmita, Chan, Michelle, Styczynsky, Mark P, Pfiffner, Jenna, French, Courtney, Socha, Amanda, Thielke, Anne, Napolitano, Sara, Muller, Paul, Kellis, Manolis, Konieczka, Jay H, Wapinski, Ilan, Regev, Aviv
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3687341/
https://www.ncbi.nlm.nih.gov/pubmed/23795289
http://dx.doi.org/10.7554/eLife.00603
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author Thompson, Dawn A
Roy, Sushmita
Chan, Michelle
Styczynsky, Mark P
Pfiffner, Jenna
French, Courtney
Socha, Amanda
Thielke, Anne
Napolitano, Sara
Muller, Paul
Kellis, Manolis
Konieczka, Jay H
Wapinski, Ilan
Regev, Aviv
author_facet Thompson, Dawn A
Roy, Sushmita
Chan, Michelle
Styczynsky, Mark P
Pfiffner, Jenna
French, Courtney
Socha, Amanda
Thielke, Anne
Napolitano, Sara
Muller, Paul
Kellis, Manolis
Konieczka, Jay H
Wapinski, Ilan
Regev, Aviv
author_sort Thompson, Dawn A
collection PubMed
description Divergence in gene regulation can play a major role in evolution. Here, we used a phylogenetic framework to measure mRNA profiles in 15 yeast species from the phylum Ascomycota and reconstruct the evolution of their modular regulatory programs along a time course of growth on glucose over 300 million years. We found that modules have diverged proportionally to phylogenetic distance, with prominent changes in gene regulation accompanying changes in lifestyle and ploidy, especially in carbon metabolism. Paralogs have significantly contributed to regulatory divergence, typically within a very short window from their duplication. Paralogs from a whole genome duplication (WGD) event have a uniquely substantial contribution that extends over a longer span. Similar patterns occur when considering the evolution of the heat shock regulatory program measured in eight of the species, suggesting that these are general evolutionary principles. DOI: http://dx.doi.org/10.7554/eLife.00603.001
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spelling pubmed-36873412013-06-21 Evolutionary principles of modular gene regulation in yeasts Thompson, Dawn A Roy, Sushmita Chan, Michelle Styczynsky, Mark P Pfiffner, Jenna French, Courtney Socha, Amanda Thielke, Anne Napolitano, Sara Muller, Paul Kellis, Manolis Konieczka, Jay H Wapinski, Ilan Regev, Aviv eLife Genomics and Evolutionary Biology Divergence in gene regulation can play a major role in evolution. Here, we used a phylogenetic framework to measure mRNA profiles in 15 yeast species from the phylum Ascomycota and reconstruct the evolution of their modular regulatory programs along a time course of growth on glucose over 300 million years. We found that modules have diverged proportionally to phylogenetic distance, with prominent changes in gene regulation accompanying changes in lifestyle and ploidy, especially in carbon metabolism. Paralogs have significantly contributed to regulatory divergence, typically within a very short window from their duplication. Paralogs from a whole genome duplication (WGD) event have a uniquely substantial contribution that extends over a longer span. Similar patterns occur when considering the evolution of the heat shock regulatory program measured in eight of the species, suggesting that these are general evolutionary principles. DOI: http://dx.doi.org/10.7554/eLife.00603.001 eLife Sciences Publications, Ltd 2013-06-18 /pmc/articles/PMC3687341/ /pubmed/23795289 http://dx.doi.org/10.7554/eLife.00603 Text en Copyright © 2013, Thompson et al http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Genomics and Evolutionary Biology
Thompson, Dawn A
Roy, Sushmita
Chan, Michelle
Styczynsky, Mark P
Pfiffner, Jenna
French, Courtney
Socha, Amanda
Thielke, Anne
Napolitano, Sara
Muller, Paul
Kellis, Manolis
Konieczka, Jay H
Wapinski, Ilan
Regev, Aviv
Evolutionary principles of modular gene regulation in yeasts
title Evolutionary principles of modular gene regulation in yeasts
title_full Evolutionary principles of modular gene regulation in yeasts
title_fullStr Evolutionary principles of modular gene regulation in yeasts
title_full_unstemmed Evolutionary principles of modular gene regulation in yeasts
title_short Evolutionary principles of modular gene regulation in yeasts
title_sort evolutionary principles of modular gene regulation in yeasts
topic Genomics and Evolutionary Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3687341/
https://www.ncbi.nlm.nih.gov/pubmed/23795289
http://dx.doi.org/10.7554/eLife.00603
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