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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2013
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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 |
format | Online Article Text |
id | pubmed-3687341 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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