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Positively selected amino acid replacements within the RuBisCO enzyme of oak trees are associated with ecological adaptations

Phylogenetic analysis by maximum likelihood (PAML) has become the standard approach to study positive selection at the molecular level, but other methods may provide complementary ways to identify amino acid replacements associated with particular conditions. Here, we compare results of the decision...

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Autores principales: Hermida-Carrera, Carmen, Fares, Mario A., Fernández, Ángel, Gil-Pelegrín, Eustaquio, Kapralov, Maxim V., Mir, Arnau, Molins, Arántzazu, Peguero-Pina, José Javier, Rocha, Jairo, Sancho-Knapik, Domingo, Galmés, Jeroni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5578625/
https://www.ncbi.nlm.nih.gov/pubmed/28859145
http://dx.doi.org/10.1371/journal.pone.0183970
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author Hermida-Carrera, Carmen
Fares, Mario A.
Fernández, Ángel
Gil-Pelegrín, Eustaquio
Kapralov, Maxim V.
Mir, Arnau
Molins, Arántzazu
Peguero-Pina, José Javier
Rocha, Jairo
Sancho-Knapik, Domingo
Galmés, Jeroni
author_facet Hermida-Carrera, Carmen
Fares, Mario A.
Fernández, Ángel
Gil-Pelegrín, Eustaquio
Kapralov, Maxim V.
Mir, Arnau
Molins, Arántzazu
Peguero-Pina, José Javier
Rocha, Jairo
Sancho-Knapik, Domingo
Galmés, Jeroni
author_sort Hermida-Carrera, Carmen
collection PubMed
description Phylogenetic analysis by maximum likelihood (PAML) has become the standard approach to study positive selection at the molecular level, but other methods may provide complementary ways to identify amino acid replacements associated with particular conditions. Here, we compare results of the decision tree (DT) model method with ones of PAML using the key photosynthetic enzyme RuBisCO as a model system to study molecular adaptation to particular ecological conditions in oaks (Quercus). We sequenced the chloroplast rbcL gene encoding RuBisCO large subunit in 158 Quercus species, covering about a third of the global genus diversity. It has been hypothesized that RuBisCO has evolved differentially depending on the environmental conditions and leaf traits governing internal gas diffusion patterns. Here, we show, using PAML, that amino acid replacements at the residue positions 95, 145, 251, 262 and 328 of the RuBisCO large subunit have been the subject of positive selection along particular Quercus lineages associated with the leaf traits and climate characteristics. In parallel, the DT model identified amino acid replacements at sites 95, 219, 262 and 328 being associated with the leaf traits and climate characteristics, exhibiting partial overlap with the results obtained using PAML.
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spelling pubmed-55786252017-09-15 Positively selected amino acid replacements within the RuBisCO enzyme of oak trees are associated with ecological adaptations Hermida-Carrera, Carmen Fares, Mario A. Fernández, Ángel Gil-Pelegrín, Eustaquio Kapralov, Maxim V. Mir, Arnau Molins, Arántzazu Peguero-Pina, José Javier Rocha, Jairo Sancho-Knapik, Domingo Galmés, Jeroni PLoS One Research Article Phylogenetic analysis by maximum likelihood (PAML) has become the standard approach to study positive selection at the molecular level, but other methods may provide complementary ways to identify amino acid replacements associated with particular conditions. Here, we compare results of the decision tree (DT) model method with ones of PAML using the key photosynthetic enzyme RuBisCO as a model system to study molecular adaptation to particular ecological conditions in oaks (Quercus). We sequenced the chloroplast rbcL gene encoding RuBisCO large subunit in 158 Quercus species, covering about a third of the global genus diversity. It has been hypothesized that RuBisCO has evolved differentially depending on the environmental conditions and leaf traits governing internal gas diffusion patterns. Here, we show, using PAML, that amino acid replacements at the residue positions 95, 145, 251, 262 and 328 of the RuBisCO large subunit have been the subject of positive selection along particular Quercus lineages associated with the leaf traits and climate characteristics. In parallel, the DT model identified amino acid replacements at sites 95, 219, 262 and 328 being associated with the leaf traits and climate characteristics, exhibiting partial overlap with the results obtained using PAML. Public Library of Science 2017-08-31 /pmc/articles/PMC5578625/ /pubmed/28859145 http://dx.doi.org/10.1371/journal.pone.0183970 Text en © 2017 Hermida-Carrera et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Hermida-Carrera, Carmen
Fares, Mario A.
Fernández, Ángel
Gil-Pelegrín, Eustaquio
Kapralov, Maxim V.
Mir, Arnau
Molins, Arántzazu
Peguero-Pina, José Javier
Rocha, Jairo
Sancho-Knapik, Domingo
Galmés, Jeroni
Positively selected amino acid replacements within the RuBisCO enzyme of oak trees are associated with ecological adaptations
title Positively selected amino acid replacements within the RuBisCO enzyme of oak trees are associated with ecological adaptations
title_full Positively selected amino acid replacements within the RuBisCO enzyme of oak trees are associated with ecological adaptations
title_fullStr Positively selected amino acid replacements within the RuBisCO enzyme of oak trees are associated with ecological adaptations
title_full_unstemmed Positively selected amino acid replacements within the RuBisCO enzyme of oak trees are associated with ecological adaptations
title_short Positively selected amino acid replacements within the RuBisCO enzyme of oak trees are associated with ecological adaptations
title_sort positively selected amino acid replacements within the rubisco enzyme of oak trees are associated with ecological adaptations
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5578625/
https://www.ncbi.nlm.nih.gov/pubmed/28859145
http://dx.doi.org/10.1371/journal.pone.0183970
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