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Parallel evolution of the make–accumulate–consume strategy in Saccharomyces and Dekkera yeasts
Saccharomyces yeasts degrade sugars to two-carbon components, in particular ethanol, even in the presence of excess oxygen. This characteristic is called the Crabtree effect and is the background for the 'make–accumulate–consume' life strategy, which in natural habitats helps Saccharomyces...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3112538/ https://www.ncbi.nlm.nih.gov/pubmed/21556056 http://dx.doi.org/10.1038/ncomms1305 |
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author | Rozpędowska, Elżbieta Hellborg, Linda Ishchuk, Olena P. Orhan, Furkan Galafassi, Silvia Merico, Annamaria Woolfit, Megan Compagno, Concetta Piškur, Jure |
author_facet | Rozpędowska, Elżbieta Hellborg, Linda Ishchuk, Olena P. Orhan, Furkan Galafassi, Silvia Merico, Annamaria Woolfit, Megan Compagno, Concetta Piškur, Jure |
author_sort | Rozpędowska, Elżbieta |
collection | PubMed |
description | Saccharomyces yeasts degrade sugars to two-carbon components, in particular ethanol, even in the presence of excess oxygen. This characteristic is called the Crabtree effect and is the background for the 'make–accumulate–consume' life strategy, which in natural habitats helps Saccharomyces yeasts to out-compete other microorganisms. A global promoter rewiring in the Saccharomyces cerevisiae lineage, which occurred around 100 mya, was one of the main molecular events providing the background for evolution of this strategy. Here we show that the Dekkera bruxellensis lineage, which separated from the Saccharomyces yeasts more than 200 mya, also efficiently makes, accumulates and consumes ethanol and acetic acid. Analysis of promoter sequences indicates that both lineages independently underwent a massive loss of a specific cis-regulatory element from dozens of genes associated with respiration, and we show that also in D. bruxellensis this promoter rewiring contributes to the observed Crabtree effect. |
format | Online Article Text |
id | pubmed-3112538 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-31125382011-06-29 Parallel evolution of the make–accumulate–consume strategy in Saccharomyces and Dekkera yeasts Rozpędowska, Elżbieta Hellborg, Linda Ishchuk, Olena P. Orhan, Furkan Galafassi, Silvia Merico, Annamaria Woolfit, Megan Compagno, Concetta Piškur, Jure Nat Commun Article Saccharomyces yeasts degrade sugars to two-carbon components, in particular ethanol, even in the presence of excess oxygen. This characteristic is called the Crabtree effect and is the background for the 'make–accumulate–consume' life strategy, which in natural habitats helps Saccharomyces yeasts to out-compete other microorganisms. A global promoter rewiring in the Saccharomyces cerevisiae lineage, which occurred around 100 mya, was one of the main molecular events providing the background for evolution of this strategy. Here we show that the Dekkera bruxellensis lineage, which separated from the Saccharomyces yeasts more than 200 mya, also efficiently makes, accumulates and consumes ethanol and acetic acid. Analysis of promoter sequences indicates that both lineages independently underwent a massive loss of a specific cis-regulatory element from dozens of genes associated with respiration, and we show that also in D. bruxellensis this promoter rewiring contributes to the observed Crabtree effect. Nature Publishing Group 2011-05 2011-05-10 /pmc/articles/PMC3112538/ /pubmed/21556056 http://dx.doi.org/10.1038/ncomms1305 Text en Copyright © 2011, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/ |
spellingShingle | Article Rozpędowska, Elżbieta Hellborg, Linda Ishchuk, Olena P. Orhan, Furkan Galafassi, Silvia Merico, Annamaria Woolfit, Megan Compagno, Concetta Piškur, Jure Parallel evolution of the make–accumulate–consume strategy in Saccharomyces and Dekkera yeasts |
title | Parallel evolution of the make–accumulate–consume strategy in Saccharomyces and Dekkera yeasts |
title_full | Parallel evolution of the make–accumulate–consume strategy in Saccharomyces and Dekkera yeasts |
title_fullStr | Parallel evolution of the make–accumulate–consume strategy in Saccharomyces and Dekkera yeasts |
title_full_unstemmed | Parallel evolution of the make–accumulate–consume strategy in Saccharomyces and Dekkera yeasts |
title_short | Parallel evolution of the make–accumulate–consume strategy in Saccharomyces and Dekkera yeasts |
title_sort | parallel evolution of the make–accumulate–consume strategy in saccharomyces and dekkera yeasts |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3112538/ https://www.ncbi.nlm.nih.gov/pubmed/21556056 http://dx.doi.org/10.1038/ncomms1305 |
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