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Diversification of defensins and NLRs in Arabidopsis species by different evolutionary mechanisms

BACKGROUND: Genes encoding proteins underlying host-pathogen co-evolution and which are selected for new resistance specificities frequently are under positive selection, a process that maintains diversity. Here, we tested the contribution of natural selection, recombination and transcriptional dive...

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Autores principales: Mondragón-Palomino, Mariana, Stam, Remco, John-Arputharaj, Ajay, Dresselhaus, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5731061/
https://www.ncbi.nlm.nih.gov/pubmed/29246101
http://dx.doi.org/10.1186/s12862-017-1099-4
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author Mondragón-Palomino, Mariana
Stam, Remco
John-Arputharaj, Ajay
Dresselhaus, Thomas
author_facet Mondragón-Palomino, Mariana
Stam, Remco
John-Arputharaj, Ajay
Dresselhaus, Thomas
author_sort Mondragón-Palomino, Mariana
collection PubMed
description BACKGROUND: Genes encoding proteins underlying host-pathogen co-evolution and which are selected for new resistance specificities frequently are under positive selection, a process that maintains diversity. Here, we tested the contribution of natural selection, recombination and transcriptional divergence to the evolutionary diversification of the plant defensins superfamily in three Arabidopsis species. The intracellular NOD-like receptor (NLR) family was used for comparison because positive selection has been well documented in its members. Similar to defensins, NLRs are encoded by a large and polymorphic gene family and many of their members are involved in the immune response. RESULTS: Gene trees of Arabidopsis defensins (DEFLs) show a high prevalence of clades containing orthologs. This indicates that their diversity dates back to a common ancestor and species-specific duplications did not significantly contribute to gene family expansion. DEFLs are characterized by a pervasive pattern of neutral evolution with infrequent positive and negative selection as well as recombination. In comparison, most NLR alignment groups are characterized by frequent occurrence of positive selection and recombination in their leucine-rich repeat (LRR) domain as well negative selection in their nucleotide-binding (NB-ARC) domain. While major NLR subgroups are expressed in pistils and leaves both in presence or absence of pathogen infection, the members of DEFL alignment groups are predominantly transcribed in pistils. Furthermore, conserved groups of NLRs and DEFLs are differentially expressed in response to Fusarium graminearum regardless of whether these genes are under positive selection or not. CONCLUSIONS: The present analyses of NLRs expands previous studies in Arabidopsis thaliana and highlights contrasting patterns of purifying and diversifying selection affecting different gene regions. DEFL genes show a different evolutionary trend, with fewer recombination events and significantly fewer instances of natural selection. Their heterogeneous expression pattern suggests that transcriptional divergence probably made the major contribution to functional diversification. In comparison to smaller families encoding pathogenesis-related (PR) proteins under positive selection, DEFLs are involved in a wide variety of processes that altogether might pose structural and functional trade-offs to their family-wide pattern of evolution. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12862-017-1099-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-57310612017-12-19 Diversification of defensins and NLRs in Arabidopsis species by different evolutionary mechanisms Mondragón-Palomino, Mariana Stam, Remco John-Arputharaj, Ajay Dresselhaus, Thomas BMC Evol Biol Research Article BACKGROUND: Genes encoding proteins underlying host-pathogen co-evolution and which are selected for new resistance specificities frequently are under positive selection, a process that maintains diversity. Here, we tested the contribution of natural selection, recombination and transcriptional divergence to the evolutionary diversification of the plant defensins superfamily in three Arabidopsis species. The intracellular NOD-like receptor (NLR) family was used for comparison because positive selection has been well documented in its members. Similar to defensins, NLRs are encoded by a large and polymorphic gene family and many of their members are involved in the immune response. RESULTS: Gene trees of Arabidopsis defensins (DEFLs) show a high prevalence of clades containing orthologs. This indicates that their diversity dates back to a common ancestor and species-specific duplications did not significantly contribute to gene family expansion. DEFLs are characterized by a pervasive pattern of neutral evolution with infrequent positive and negative selection as well as recombination. In comparison, most NLR alignment groups are characterized by frequent occurrence of positive selection and recombination in their leucine-rich repeat (LRR) domain as well negative selection in their nucleotide-binding (NB-ARC) domain. While major NLR subgroups are expressed in pistils and leaves both in presence or absence of pathogen infection, the members of DEFL alignment groups are predominantly transcribed in pistils. Furthermore, conserved groups of NLRs and DEFLs are differentially expressed in response to Fusarium graminearum regardless of whether these genes are under positive selection or not. CONCLUSIONS: The present analyses of NLRs expands previous studies in Arabidopsis thaliana and highlights contrasting patterns of purifying and diversifying selection affecting different gene regions. DEFL genes show a different evolutionary trend, with fewer recombination events and significantly fewer instances of natural selection. Their heterogeneous expression pattern suggests that transcriptional divergence probably made the major contribution to functional diversification. In comparison to smaller families encoding pathogenesis-related (PR) proteins under positive selection, DEFLs are involved in a wide variety of processes that altogether might pose structural and functional trade-offs to their family-wide pattern of evolution. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12862-017-1099-4) contains supplementary material, which is available to authorized users. BioMed Central 2017-12-15 /pmc/articles/PMC5731061/ /pubmed/29246101 http://dx.doi.org/10.1186/s12862-017-1099-4 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Mondragón-Palomino, Mariana
Stam, Remco
John-Arputharaj, Ajay
Dresselhaus, Thomas
Diversification of defensins and NLRs in Arabidopsis species by different evolutionary mechanisms
title Diversification of defensins and NLRs in Arabidopsis species by different evolutionary mechanisms
title_full Diversification of defensins and NLRs in Arabidopsis species by different evolutionary mechanisms
title_fullStr Diversification of defensins and NLRs in Arabidopsis species by different evolutionary mechanisms
title_full_unstemmed Diversification of defensins and NLRs in Arabidopsis species by different evolutionary mechanisms
title_short Diversification of defensins and NLRs in Arabidopsis species by different evolutionary mechanisms
title_sort diversification of defensins and nlrs in arabidopsis species by different evolutionary mechanisms
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5731061/
https://www.ncbi.nlm.nih.gov/pubmed/29246101
http://dx.doi.org/10.1186/s12862-017-1099-4
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