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Allelic compatibility in plant immune receptors facilitates engineering of new effector recognition specificities

Engineering the plant immune system offers genetic solutions to mitigate crop diseases caused by diverse agriculturally significant pathogens and pests. Modification of intracellular plant immune receptors of the nucleotide-binding leucine-rich repeat (NLR) receptor superfamily for expanded recognit...

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Autores principales: Bentham, Adam R, De la Concepcion, Juan Carlos, Benjumea, Javier Vega, Kourelis, Jiorgos, Jones, Sally, Mendel, Melanie, Stubbs, Jack, Stevenson, Clare E M, Maidment, Josephine H R, Youles, Mark, Zdrzałek, Rafał, Kamoun, Sophien, Banfield, Mark J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10533329/
https://www.ncbi.nlm.nih.gov/pubmed/37486356
http://dx.doi.org/10.1093/plcell/koad204
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author Bentham, Adam R
De la Concepcion, Juan Carlos
Benjumea, Javier Vega
Kourelis, Jiorgos
Jones, Sally
Mendel, Melanie
Stubbs, Jack
Stevenson, Clare E M
Maidment, Josephine H R
Youles, Mark
Zdrzałek, Rafał
Kamoun, Sophien
Banfield, Mark J
author_facet Bentham, Adam R
De la Concepcion, Juan Carlos
Benjumea, Javier Vega
Kourelis, Jiorgos
Jones, Sally
Mendel, Melanie
Stubbs, Jack
Stevenson, Clare E M
Maidment, Josephine H R
Youles, Mark
Zdrzałek, Rafał
Kamoun, Sophien
Banfield, Mark J
author_sort Bentham, Adam R
collection PubMed
description Engineering the plant immune system offers genetic solutions to mitigate crop diseases caused by diverse agriculturally significant pathogens and pests. Modification of intracellular plant immune receptors of the nucleotide-binding leucine-rich repeat (NLR) receptor superfamily for expanded recognition of pathogen virulence proteins (effectors) is a promising approach for engineering disease resistance. However, engineering can cause NLR autoactivation, resulting in constitutive defense responses that are deleterious to the plant. This may be due to plant NLRs associating in highly complex signaling networks that coevolve together, and changes through breeding or genetic modification can generate incompatible combinations, resulting in autoimmune phenotypes. The sensor and helper NLRs of the rice (Oryza sativa) NLR pair Pik have coevolved, and mismatching between noncoevolved alleles triggers constitutive activation and cell death. This limits the extent to which protein modifications can be used to engineer pathogen recognition and enhance disease resistance mediated by these NLRs. Here, we dissected incompatibility determinants in the Pik pair in Nicotiana benthamiana and found that heavy metal–associated (HMA) domains integrated in Pik-1 not only evolved to bind pathogen effectors but also likely coevolved with other NLR domains to maintain immune homeostasis. This explains why changes in integrated domains can lead to autoactivation. We then used this knowledge to facilitate engineering of new effector recognition specificities, overcoming initial autoimmune penalties. We show that by mismatching alleles of the rice sensor and helper NLRs Pik-1 and Pik-2, we can enable the integration of synthetic domains with novel and enhanced recognition specificities. Taken together, our results reveal a strategy for engineering NLRs, which has the potential to allow an expanded set of integrations and therefore new disease resistance specificities in plants.
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spelling pubmed-105333292023-09-28 Allelic compatibility in plant immune receptors facilitates engineering of new effector recognition specificities Bentham, Adam R De la Concepcion, Juan Carlos Benjumea, Javier Vega Kourelis, Jiorgos Jones, Sally Mendel, Melanie Stubbs, Jack Stevenson, Clare E M Maidment, Josephine H R Youles, Mark Zdrzałek, Rafał Kamoun, Sophien Banfield, Mark J Plant Cell Research Article Engineering the plant immune system offers genetic solutions to mitigate crop diseases caused by diverse agriculturally significant pathogens and pests. Modification of intracellular plant immune receptors of the nucleotide-binding leucine-rich repeat (NLR) receptor superfamily for expanded recognition of pathogen virulence proteins (effectors) is a promising approach for engineering disease resistance. However, engineering can cause NLR autoactivation, resulting in constitutive defense responses that are deleterious to the plant. This may be due to plant NLRs associating in highly complex signaling networks that coevolve together, and changes through breeding or genetic modification can generate incompatible combinations, resulting in autoimmune phenotypes. The sensor and helper NLRs of the rice (Oryza sativa) NLR pair Pik have coevolved, and mismatching between noncoevolved alleles triggers constitutive activation and cell death. This limits the extent to which protein modifications can be used to engineer pathogen recognition and enhance disease resistance mediated by these NLRs. Here, we dissected incompatibility determinants in the Pik pair in Nicotiana benthamiana and found that heavy metal–associated (HMA) domains integrated in Pik-1 not only evolved to bind pathogen effectors but also likely coevolved with other NLR domains to maintain immune homeostasis. This explains why changes in integrated domains can lead to autoactivation. We then used this knowledge to facilitate engineering of new effector recognition specificities, overcoming initial autoimmune penalties. We show that by mismatching alleles of the rice sensor and helper NLRs Pik-1 and Pik-2, we can enable the integration of synthetic domains with novel and enhanced recognition specificities. Taken together, our results reveal a strategy for engineering NLRs, which has the potential to allow an expanded set of integrations and therefore new disease resistance specificities in plants. Oxford University Press 2023-07-24 /pmc/articles/PMC10533329/ /pubmed/37486356 http://dx.doi.org/10.1093/plcell/koad204 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of American Society of Plant Biologists. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Bentham, Adam R
De la Concepcion, Juan Carlos
Benjumea, Javier Vega
Kourelis, Jiorgos
Jones, Sally
Mendel, Melanie
Stubbs, Jack
Stevenson, Clare E M
Maidment, Josephine H R
Youles, Mark
Zdrzałek, Rafał
Kamoun, Sophien
Banfield, Mark J
Allelic compatibility in plant immune receptors facilitates engineering of new effector recognition specificities
title Allelic compatibility in plant immune receptors facilitates engineering of new effector recognition specificities
title_full Allelic compatibility in plant immune receptors facilitates engineering of new effector recognition specificities
title_fullStr Allelic compatibility in plant immune receptors facilitates engineering of new effector recognition specificities
title_full_unstemmed Allelic compatibility in plant immune receptors facilitates engineering of new effector recognition specificities
title_short Allelic compatibility in plant immune receptors facilitates engineering of new effector recognition specificities
title_sort allelic compatibility in plant immune receptors facilitates engineering of new effector recognition specificities
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10533329/
https://www.ncbi.nlm.nih.gov/pubmed/37486356
http://dx.doi.org/10.1093/plcell/koad204
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