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Adaptive evolution of complex innovations through stepwise metabolic niche expansion
A central challenge in evolutionary biology concerns the mechanisms by which complex metabolic innovations requiring multiple mutations arise. Here, we propose that metabolic innovations accessible through the addition of a single reaction serve as stepping stones towards the later establishment of...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5411730/ https://www.ncbi.nlm.nih.gov/pubmed/27197754 http://dx.doi.org/10.1038/ncomms11607 |
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author | Szappanos, Balázs Fritzemeier, Jonathan Csörgő, Bálint Lázár, Viktória Lu, Xiaowen Fekete, Gergely Bálint, Balázs Herczeg, Róbert Nagy, István Notebaart, Richard A. Lercher, Martin J. Pál, Csaba Papp, Balázs |
author_facet | Szappanos, Balázs Fritzemeier, Jonathan Csörgő, Bálint Lázár, Viktória Lu, Xiaowen Fekete, Gergely Bálint, Balázs Herczeg, Róbert Nagy, István Notebaart, Richard A. Lercher, Martin J. Pál, Csaba Papp, Balázs |
author_sort | Szappanos, Balázs |
collection | PubMed |
description | A central challenge in evolutionary biology concerns the mechanisms by which complex metabolic innovations requiring multiple mutations arise. Here, we propose that metabolic innovations accessible through the addition of a single reaction serve as stepping stones towards the later establishment of complex metabolic features in another environment. We demonstrate the feasibility of this hypothesis through three complementary analyses. First, using genome-scale metabolic modelling, we show that complex metabolic innovations in Escherichia coli can arise via changing nutrient conditions. Second, using phylogenetic approaches, we demonstrate that the acquisition patterns of complex metabolic pathways during the evolutionary history of bacterial genomes support the hypothesis. Third, we show how adaptation of laboratory populations of E. coli to one carbon source facilitates the later adaptation to another carbon source. Our work demonstrates how complex innovations can evolve through series of adaptive steps without the need to invoke non-adaptive processes. |
format | Online Article Text |
id | pubmed-5411730 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-54117302017-07-11 Adaptive evolution of complex innovations through stepwise metabolic niche expansion Szappanos, Balázs Fritzemeier, Jonathan Csörgő, Bálint Lázár, Viktória Lu, Xiaowen Fekete, Gergely Bálint, Balázs Herczeg, Róbert Nagy, István Notebaart, Richard A. Lercher, Martin J. Pál, Csaba Papp, Balázs Nat Commun Article A central challenge in evolutionary biology concerns the mechanisms by which complex metabolic innovations requiring multiple mutations arise. Here, we propose that metabolic innovations accessible through the addition of a single reaction serve as stepping stones towards the later establishment of complex metabolic features in another environment. We demonstrate the feasibility of this hypothesis through three complementary analyses. First, using genome-scale metabolic modelling, we show that complex metabolic innovations in Escherichia coli can arise via changing nutrient conditions. Second, using phylogenetic approaches, we demonstrate that the acquisition patterns of complex metabolic pathways during the evolutionary history of bacterial genomes support the hypothesis. Third, we show how adaptation of laboratory populations of E. coli to one carbon source facilitates the later adaptation to another carbon source. Our work demonstrates how complex innovations can evolve through series of adaptive steps without the need to invoke non-adaptive processes. Nature Publishing Group 2016-05-20 /pmc/articles/PMC5411730/ /pubmed/27197754 http://dx.doi.org/10.1038/ncomms11607 Text en Copyright © 2016, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Szappanos, Balázs Fritzemeier, Jonathan Csörgő, Bálint Lázár, Viktória Lu, Xiaowen Fekete, Gergely Bálint, Balázs Herczeg, Róbert Nagy, István Notebaart, Richard A. Lercher, Martin J. Pál, Csaba Papp, Balázs Adaptive evolution of complex innovations through stepwise metabolic niche expansion |
title | Adaptive evolution of complex innovations through stepwise metabolic niche expansion |
title_full | Adaptive evolution of complex innovations through stepwise metabolic niche expansion |
title_fullStr | Adaptive evolution of complex innovations through stepwise metabolic niche expansion |
title_full_unstemmed | Adaptive evolution of complex innovations through stepwise metabolic niche expansion |
title_short | Adaptive evolution of complex innovations through stepwise metabolic niche expansion |
title_sort | adaptive evolution of complex innovations through stepwise metabolic niche expansion |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5411730/ https://www.ncbi.nlm.nih.gov/pubmed/27197754 http://dx.doi.org/10.1038/ncomms11607 |
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