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A phylogenetic analysis of macroevolutionary patterns in fermentative yeasts

When novel sources of ecological opportunity are available, physiological innovations can trigger adaptive radiations. This could be the case of yeasts (Saccharomycotina), in which an evolutionary novelty is represented by the capacity to exploit simple sugars from fruits (fermentation). During adap...

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Autores principales: Paleo‐López, Rocío, Quintero‐Galvis, Julian F., Solano‐Iguaran, Jaiber J., Sanchez‐Salazar, Angela M., Gaitan‐Espitia, Juan D., Nespolo, Roberto F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4972215/
https://www.ncbi.nlm.nih.gov/pubmed/27516851
http://dx.doi.org/10.1002/ece3.2097
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author Paleo‐López, Rocío
Quintero‐Galvis, Julian F.
Solano‐Iguaran, Jaiber J.
Sanchez‐Salazar, Angela M.
Gaitan‐Espitia, Juan D.
Nespolo, Roberto F.
author_facet Paleo‐López, Rocío
Quintero‐Galvis, Julian F.
Solano‐Iguaran, Jaiber J.
Sanchez‐Salazar, Angela M.
Gaitan‐Espitia, Juan D.
Nespolo, Roberto F.
author_sort Paleo‐López, Rocío
collection PubMed
description When novel sources of ecological opportunity are available, physiological innovations can trigger adaptive radiations. This could be the case of yeasts (Saccharomycotina), in which an evolutionary novelty is represented by the capacity to exploit simple sugars from fruits (fermentation). During adaptive radiations, diversification and morphological evolution are predicted to slow‐down after early bursts of diversification. Here, we performed the first comparative phylogenetic analysis in yeasts, testing the “early burst” prediction on species diversification and also on traits of putative ecological relevance (cell‐size and fermentation versatility). We found that speciation rates are constant during the time‐range we considered (ca., 150 millions of years). Phylogenetic signal of both traits was significant (but lower for cell‐size), suggesting that lineages resemble each other in trait‐values. Disparity analysis suggested accelerated evolution (diversification in trait values above Brownian Motion expectations) in cell‐size. We also found a significant phylogenetic regression between cell‐size and fermentation versatility (R (2) = 0.10), which suggests correlated evolution between both traits. Overall, our results do not support the early burst prediction both in species and traits, but suggest a number of interesting evolutionary patterns, that warrant further exploration. For instance, we show that the Whole Genomic Duplication that affected a whole clade of yeasts, does not seems to have a statistically detectable phenotypic effect at our level of analysis. In this regard, further studies of fermentation under common‐garden conditions combined with comparative analyses are warranted.
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spelling pubmed-49722152016-08-11 A phylogenetic analysis of macroevolutionary patterns in fermentative yeasts Paleo‐López, Rocío Quintero‐Galvis, Julian F. Solano‐Iguaran, Jaiber J. Sanchez‐Salazar, Angela M. Gaitan‐Espitia, Juan D. Nespolo, Roberto F. Ecol Evol Original Research When novel sources of ecological opportunity are available, physiological innovations can trigger adaptive radiations. This could be the case of yeasts (Saccharomycotina), in which an evolutionary novelty is represented by the capacity to exploit simple sugars from fruits (fermentation). During adaptive radiations, diversification and morphological evolution are predicted to slow‐down after early bursts of diversification. Here, we performed the first comparative phylogenetic analysis in yeasts, testing the “early burst” prediction on species diversification and also on traits of putative ecological relevance (cell‐size and fermentation versatility). We found that speciation rates are constant during the time‐range we considered (ca., 150 millions of years). Phylogenetic signal of both traits was significant (but lower for cell‐size), suggesting that lineages resemble each other in trait‐values. Disparity analysis suggested accelerated evolution (diversification in trait values above Brownian Motion expectations) in cell‐size. We also found a significant phylogenetic regression between cell‐size and fermentation versatility (R (2) = 0.10), which suggests correlated evolution between both traits. Overall, our results do not support the early burst prediction both in species and traits, but suggest a number of interesting evolutionary patterns, that warrant further exploration. For instance, we show that the Whole Genomic Duplication that affected a whole clade of yeasts, does not seems to have a statistically detectable phenotypic effect at our level of analysis. In this regard, further studies of fermentation under common‐garden conditions combined with comparative analyses are warranted. John Wiley and Sons Inc. 2016-05-10 /pmc/articles/PMC4972215/ /pubmed/27516851 http://dx.doi.org/10.1002/ece3.2097 Text en © 2016 The Authors. Ecology and Evolution published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Paleo‐López, Rocío
Quintero‐Galvis, Julian F.
Solano‐Iguaran, Jaiber J.
Sanchez‐Salazar, Angela M.
Gaitan‐Espitia, Juan D.
Nespolo, Roberto F.
A phylogenetic analysis of macroevolutionary patterns in fermentative yeasts
title A phylogenetic analysis of macroevolutionary patterns in fermentative yeasts
title_full A phylogenetic analysis of macroevolutionary patterns in fermentative yeasts
title_fullStr A phylogenetic analysis of macroevolutionary patterns in fermentative yeasts
title_full_unstemmed A phylogenetic analysis of macroevolutionary patterns in fermentative yeasts
title_short A phylogenetic analysis of macroevolutionary patterns in fermentative yeasts
title_sort phylogenetic analysis of macroevolutionary patterns in fermentative yeasts
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4972215/
https://www.ncbi.nlm.nih.gov/pubmed/27516851
http://dx.doi.org/10.1002/ece3.2097
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