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Decoupled genomic elements and the evolution of partner quality in nitrogen‐fixing rhizobia

Understanding how mutualisms evolve in response to a changing environment will be critical for predicting the long‐term impacts of global changes, such as increased N (nitrogen) deposition. Bacterial mutualists in particular might evolve quickly, thanks to short generation times and the potential fo...

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Autores principales: Gordon, Benjamin R., Klinger, Christie R., Weese, Dylan J., Lau, Jennifer A., Burke, Patricia V., Dentinger, Bryn T. M., Heath, Katy D.
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/PMC4775534/
https://www.ncbi.nlm.nih.gov/pubmed/27087920
http://dx.doi.org/10.1002/ece3.1953
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author Gordon, Benjamin R.
Klinger, Christie R.
Weese, Dylan J.
Lau, Jennifer A.
Burke, Patricia V.
Dentinger, Bryn T. M.
Heath, Katy D.
author_facet Gordon, Benjamin R.
Klinger, Christie R.
Weese, Dylan J.
Lau, Jennifer A.
Burke, Patricia V.
Dentinger, Bryn T. M.
Heath, Katy D.
author_sort Gordon, Benjamin R.
collection PubMed
description Understanding how mutualisms evolve in response to a changing environment will be critical for predicting the long‐term impacts of global changes, such as increased N (nitrogen) deposition. Bacterial mutualists in particular might evolve quickly, thanks to short generation times and the potential for independent evolution of plasmids through recombination and/or HGT (horizontal gene transfer). In a previous work using the legume/rhizobia mutualism, we demonstrated that long‐term nitrogen fertilization caused the evolution of less‐mutualistic rhizobia. Here, we use our 63 previously isolated rhizobium strains in comparative phylogenetic and quantitative genetic analyses to determine the degree to which variation in partner quality is attributable to phylogenetic relationships among strains versus recent genetic changes in response to N fertilization. We find evidence of distinct evolutionary relationships between chromosomal and pSym genes, and broad similarity between pSym genes. We also find that nifD has a unique evolutionary history that explains much of the variation in partner quality, and suggest MoFe subunit interaction sites in the evolution of less‐mutualistic rhizobia. These results provide insight into the mechanisms behind the evolutionary response of rhizobia to long‐term N fertilization, and we discuss the implications of our results for the evolution of the mutualism.
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spelling pubmed-47755342016-04-15 Decoupled genomic elements and the evolution of partner quality in nitrogen‐fixing rhizobia Gordon, Benjamin R. Klinger, Christie R. Weese, Dylan J. Lau, Jennifer A. Burke, Patricia V. Dentinger, Bryn T. M. Heath, Katy D. Ecol Evol Original Research Understanding how mutualisms evolve in response to a changing environment will be critical for predicting the long‐term impacts of global changes, such as increased N (nitrogen) deposition. Bacterial mutualists in particular might evolve quickly, thanks to short generation times and the potential for independent evolution of plasmids through recombination and/or HGT (horizontal gene transfer). In a previous work using the legume/rhizobia mutualism, we demonstrated that long‐term nitrogen fertilization caused the evolution of less‐mutualistic rhizobia. Here, we use our 63 previously isolated rhizobium strains in comparative phylogenetic and quantitative genetic analyses to determine the degree to which variation in partner quality is attributable to phylogenetic relationships among strains versus recent genetic changes in response to N fertilization. We find evidence of distinct evolutionary relationships between chromosomal and pSym genes, and broad similarity between pSym genes. We also find that nifD has a unique evolutionary history that explains much of the variation in partner quality, and suggest MoFe subunit interaction sites in the evolution of less‐mutualistic rhizobia. These results provide insight into the mechanisms behind the evolutionary response of rhizobia to long‐term N fertilization, and we discuss the implications of our results for the evolution of the mutualism. John Wiley and Sons Inc. 2016-01-28 /pmc/articles/PMC4775534/ /pubmed/27087920 http://dx.doi.org/10.1002/ece3.1953 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
Gordon, Benjamin R.
Klinger, Christie R.
Weese, Dylan J.
Lau, Jennifer A.
Burke, Patricia V.
Dentinger, Bryn T. M.
Heath, Katy D.
Decoupled genomic elements and the evolution of partner quality in nitrogen‐fixing rhizobia
title Decoupled genomic elements and the evolution of partner quality in nitrogen‐fixing rhizobia
title_full Decoupled genomic elements and the evolution of partner quality in nitrogen‐fixing rhizobia
title_fullStr Decoupled genomic elements and the evolution of partner quality in nitrogen‐fixing rhizobia
title_full_unstemmed Decoupled genomic elements and the evolution of partner quality in nitrogen‐fixing rhizobia
title_short Decoupled genomic elements and the evolution of partner quality in nitrogen‐fixing rhizobia
title_sort decoupled genomic elements and the evolution of partner quality in nitrogen‐fixing rhizobia
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4775534/
https://www.ncbi.nlm.nih.gov/pubmed/27087920
http://dx.doi.org/10.1002/ece3.1953
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