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A single evolutionary innovation drives the deep evolution of symbiotic N(2)-fixation in angiosperms

Symbiotic associations occur in every habitat on earth, but we know very little about their evolutionary histories. Current models of trait evolution cannot adequately reconstruct the deep history of symbiotic innovation, because they assume homogenous evolutionary processes across millions of years...

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Autores principales: Werner, Gijsbert D. A., Cornwell, William K., Sprent, Janet I., Kattge, Jens, Kiers, E. Toby
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Pub. Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4059933/
https://www.ncbi.nlm.nih.gov/pubmed/24912610
http://dx.doi.org/10.1038/ncomms5087
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author Werner, Gijsbert D. A.
Cornwell, William K.
Sprent, Janet I.
Kattge, Jens
Kiers, E. Toby
author_facet Werner, Gijsbert D. A.
Cornwell, William K.
Sprent, Janet I.
Kattge, Jens
Kiers, E. Toby
author_sort Werner, Gijsbert D. A.
collection PubMed
description Symbiotic associations occur in every habitat on earth, but we know very little about their evolutionary histories. Current models of trait evolution cannot adequately reconstruct the deep history of symbiotic innovation, because they assume homogenous evolutionary processes across millions of years. Here we use a recently developed, heterogeneous and quantitative phylogenetic framework to study the origin of the symbiosis between angiosperms and nitrogen-fixing (N(2)) bacterial symbionts housed in nodules. We compile the largest database of global nodulating plant species and reconstruct the symbiosis’ evolution. We identify a single, cryptic evolutionary innovation driving symbiotic N(2)-fixation evolution, followed by multiple gains and losses of the symbiosis, and the subsequent emergence of ‘stable fixers’ (clades extremely unlikely to lose the symbiosis). Originating over 100 MYA, this innovation suggests deep homology in symbiotic N(2)-fixation. Identifying cryptic innovations on the tree of life is key to understanding the evolution of complex traits, including symbiotic partnerships.
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spelling pubmed-40599332014-06-18 A single evolutionary innovation drives the deep evolution of symbiotic N(2)-fixation in angiosperms Werner, Gijsbert D. A. Cornwell, William K. Sprent, Janet I. Kattge, Jens Kiers, E. Toby Nat Commun Article Symbiotic associations occur in every habitat on earth, but we know very little about their evolutionary histories. Current models of trait evolution cannot adequately reconstruct the deep history of symbiotic innovation, because they assume homogenous evolutionary processes across millions of years. Here we use a recently developed, heterogeneous and quantitative phylogenetic framework to study the origin of the symbiosis between angiosperms and nitrogen-fixing (N(2)) bacterial symbionts housed in nodules. We compile the largest database of global nodulating plant species and reconstruct the symbiosis’ evolution. We identify a single, cryptic evolutionary innovation driving symbiotic N(2)-fixation evolution, followed by multiple gains and losses of the symbiosis, and the subsequent emergence of ‘stable fixers’ (clades extremely unlikely to lose the symbiosis). Originating over 100 MYA, this innovation suggests deep homology in symbiotic N(2)-fixation. Identifying cryptic innovations on the tree of life is key to understanding the evolution of complex traits, including symbiotic partnerships. Nature Pub. Group 2014-06-10 /pmc/articles/PMC4059933/ /pubmed/24912610 http://dx.doi.org/10.1038/ncomms5087 Text en Copyright © 2014, 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-ShareAlike 4.0 Unported 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-nc-sa/4.0/
spellingShingle Article
Werner, Gijsbert D. A.
Cornwell, William K.
Sprent, Janet I.
Kattge, Jens
Kiers, E. Toby
A single evolutionary innovation drives the deep evolution of symbiotic N(2)-fixation in angiosperms
title A single evolutionary innovation drives the deep evolution of symbiotic N(2)-fixation in angiosperms
title_full A single evolutionary innovation drives the deep evolution of symbiotic N(2)-fixation in angiosperms
title_fullStr A single evolutionary innovation drives the deep evolution of symbiotic N(2)-fixation in angiosperms
title_full_unstemmed A single evolutionary innovation drives the deep evolution of symbiotic N(2)-fixation in angiosperms
title_short A single evolutionary innovation drives the deep evolution of symbiotic N(2)-fixation in angiosperms
title_sort single evolutionary innovation drives the deep evolution of symbiotic n(2)-fixation in angiosperms
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4059933/
https://www.ncbi.nlm.nih.gov/pubmed/24912610
http://dx.doi.org/10.1038/ncomms5087
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