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Functional diversification gave rise to allelic specialization in a rice NLR immune receptor pair

Cooperation between receptors from the nucleotide-binding, leucine-rich repeats (NLR) superfamily is important for intracellular activation of immune responses. NLRs can function in pairs that, upon pathogen recognition, trigger hypersensitive cell death and stop pathogen invasion. Natural selection...

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Autores principales: De la Concepcion, Juan Carlos, Vega Benjumea, Javier, Bialas, Aleksandra, Terauchi, Ryohei, Kamoun, Sophien, Banfield, Mark J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8631799/
https://www.ncbi.nlm.nih.gov/pubmed/34783652
http://dx.doi.org/10.7554/eLife.71662
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author De la Concepcion, Juan Carlos
Vega Benjumea, Javier
Bialas, Aleksandra
Terauchi, Ryohei
Kamoun, Sophien
Banfield, Mark J
author_facet De la Concepcion, Juan Carlos
Vega Benjumea, Javier
Bialas, Aleksandra
Terauchi, Ryohei
Kamoun, Sophien
Banfield, Mark J
author_sort De la Concepcion, Juan Carlos
collection PubMed
description Cooperation between receptors from the nucleotide-binding, leucine-rich repeats (NLR) superfamily is important for intracellular activation of immune responses. NLRs can function in pairs that, upon pathogen recognition, trigger hypersensitive cell death and stop pathogen invasion. Natural selection drives specialization of host immune receptors towards an optimal response, whilst keeping a tight regulation of immunity in the absence of pathogens. However, the molecular basis of co-adaptation and specialization between paired NLRs remains largely unknown. Here, we describe functional specialization in alleles of the rice NLR pair Pik that confers resistance to strains of the blast fungus Magnaporthe oryzae harbouring AVR-Pik effectors. We revealed that matching pairs of allelic Pik NLRs mount effective immune responses, whereas mismatched pairs lead to autoimmune phenotypes, a hallmark of hybrid necrosis in both natural and domesticated plant populations. We further showed that allelic specialization is largely underpinned by a single amino acid polymorphism that determines preferential association between matching pairs of Pik NLRs. These results provide a framework for how functionally linked immune receptors undergo co-adaptation to provide an effective and regulated immune response against pathogens. Understanding the molecular constraints that shape paired NLR evolution has implications beyond plant immunity given that hybrid necrosis can drive reproductive isolation.
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spelling pubmed-86317992021-12-01 Functional diversification gave rise to allelic specialization in a rice NLR immune receptor pair De la Concepcion, Juan Carlos Vega Benjumea, Javier Bialas, Aleksandra Terauchi, Ryohei Kamoun, Sophien Banfield, Mark J eLife Plant Biology Cooperation between receptors from the nucleotide-binding, leucine-rich repeats (NLR) superfamily is important for intracellular activation of immune responses. NLRs can function in pairs that, upon pathogen recognition, trigger hypersensitive cell death and stop pathogen invasion. Natural selection drives specialization of host immune receptors towards an optimal response, whilst keeping a tight regulation of immunity in the absence of pathogens. However, the molecular basis of co-adaptation and specialization between paired NLRs remains largely unknown. Here, we describe functional specialization in alleles of the rice NLR pair Pik that confers resistance to strains of the blast fungus Magnaporthe oryzae harbouring AVR-Pik effectors. We revealed that matching pairs of allelic Pik NLRs mount effective immune responses, whereas mismatched pairs lead to autoimmune phenotypes, a hallmark of hybrid necrosis in both natural and domesticated plant populations. We further showed that allelic specialization is largely underpinned by a single amino acid polymorphism that determines preferential association between matching pairs of Pik NLRs. These results provide a framework for how functionally linked immune receptors undergo co-adaptation to provide an effective and regulated immune response against pathogens. Understanding the molecular constraints that shape paired NLR evolution has implications beyond plant immunity given that hybrid necrosis can drive reproductive isolation. eLife Sciences Publications, Ltd 2021-11-16 /pmc/articles/PMC8631799/ /pubmed/34783652 http://dx.doi.org/10.7554/eLife.71662 Text en © 2021, De la Concepcion et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Plant Biology
De la Concepcion, Juan Carlos
Vega Benjumea, Javier
Bialas, Aleksandra
Terauchi, Ryohei
Kamoun, Sophien
Banfield, Mark J
Functional diversification gave rise to allelic specialization in a rice NLR immune receptor pair
title Functional diversification gave rise to allelic specialization in a rice NLR immune receptor pair
title_full Functional diversification gave rise to allelic specialization in a rice NLR immune receptor pair
title_fullStr Functional diversification gave rise to allelic specialization in a rice NLR immune receptor pair
title_full_unstemmed Functional diversification gave rise to allelic specialization in a rice NLR immune receptor pair
title_short Functional diversification gave rise to allelic specialization in a rice NLR immune receptor pair
title_sort functional diversification gave rise to allelic specialization in a rice nlr immune receptor pair
topic Plant Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8631799/
https://www.ncbi.nlm.nih.gov/pubmed/34783652
http://dx.doi.org/10.7554/eLife.71662
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