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An Overview of PRR- and NLR-Mediated Immunities: Conserved Signaling Components across the Plant Kingdom That Communicate Both Pathways

Cell-surface-localized pattern recognition receptors (PRRs) and intracellular nucleotide-binding domain and leucine-rich repeat receptors (NLRs) are plant immune proteins that trigger an orchestrated downstream signaling in response to molecules of microbial origin or host plant origin. Historically...

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Autores principales: Ramírez-Zavaleta, Candy Yuriria, García-Barrera, Laura Jeannette, Rodríguez-Verástegui, Lizette Liliana, Arrieta-Flores, Daniela, Gregorio-Jorge, Josefat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9654257/
https://www.ncbi.nlm.nih.gov/pubmed/36361764
http://dx.doi.org/10.3390/ijms232112974
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author Ramírez-Zavaleta, Candy Yuriria
García-Barrera, Laura Jeannette
Rodríguez-Verástegui, Lizette Liliana
Arrieta-Flores, Daniela
Gregorio-Jorge, Josefat
author_facet Ramírez-Zavaleta, Candy Yuriria
García-Barrera, Laura Jeannette
Rodríguez-Verástegui, Lizette Liliana
Arrieta-Flores, Daniela
Gregorio-Jorge, Josefat
author_sort Ramírez-Zavaleta, Candy Yuriria
collection PubMed
description Cell-surface-localized pattern recognition receptors (PRRs) and intracellular nucleotide-binding domain and leucine-rich repeat receptors (NLRs) are plant immune proteins that trigger an orchestrated downstream signaling in response to molecules of microbial origin or host plant origin. Historically, PRRs have been associated with pattern-triggered immunity (PTI), whereas NLRs have been involved with effector-triggered immunity (ETI). However, recent studies reveal that such binary distinction is far from being applicable to the real world. Although the perception of plant pathogens and the final mounting response are achieved by different means, central hubs involved in signaling are shared between PTI and ETI, blurring the zig-zag model of plant immunity. In this review, we not only summarize our current understanding of PRR- and NLR-mediated immunities in plants, but also highlight those signaling components that are evolutionarily conserved across the plant kingdom. Altogether, we attempt to offer an overview of how plants mediate and integrate the induction of the defense responses that comprise PTI and ETI, emphasizing the need for more evolutionary molecular plant–microbe interactions (EvoMPMI) studies that will pave the way to a better understanding of the emergence of the core molecular machinery involved in the so-called evolutionary arms race between plants and microbes.
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spelling pubmed-96542572022-11-15 An Overview of PRR- and NLR-Mediated Immunities: Conserved Signaling Components across the Plant Kingdom That Communicate Both Pathways Ramírez-Zavaleta, Candy Yuriria García-Barrera, Laura Jeannette Rodríguez-Verástegui, Lizette Liliana Arrieta-Flores, Daniela Gregorio-Jorge, Josefat Int J Mol Sci Review Cell-surface-localized pattern recognition receptors (PRRs) and intracellular nucleotide-binding domain and leucine-rich repeat receptors (NLRs) are plant immune proteins that trigger an orchestrated downstream signaling in response to molecules of microbial origin or host plant origin. Historically, PRRs have been associated with pattern-triggered immunity (PTI), whereas NLRs have been involved with effector-triggered immunity (ETI). However, recent studies reveal that such binary distinction is far from being applicable to the real world. Although the perception of plant pathogens and the final mounting response are achieved by different means, central hubs involved in signaling are shared between PTI and ETI, blurring the zig-zag model of plant immunity. In this review, we not only summarize our current understanding of PRR- and NLR-mediated immunities in plants, but also highlight those signaling components that are evolutionarily conserved across the plant kingdom. Altogether, we attempt to offer an overview of how plants mediate and integrate the induction of the defense responses that comprise PTI and ETI, emphasizing the need for more evolutionary molecular plant–microbe interactions (EvoMPMI) studies that will pave the way to a better understanding of the emergence of the core molecular machinery involved in the so-called evolutionary arms race between plants and microbes. MDPI 2022-10-26 /pmc/articles/PMC9654257/ /pubmed/36361764 http://dx.doi.org/10.3390/ijms232112974 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Ramírez-Zavaleta, Candy Yuriria
García-Barrera, Laura Jeannette
Rodríguez-Verástegui, Lizette Liliana
Arrieta-Flores, Daniela
Gregorio-Jorge, Josefat
An Overview of PRR- and NLR-Mediated Immunities: Conserved Signaling Components across the Plant Kingdom That Communicate Both Pathways
title An Overview of PRR- and NLR-Mediated Immunities: Conserved Signaling Components across the Plant Kingdom That Communicate Both Pathways
title_full An Overview of PRR- and NLR-Mediated Immunities: Conserved Signaling Components across the Plant Kingdom That Communicate Both Pathways
title_fullStr An Overview of PRR- and NLR-Mediated Immunities: Conserved Signaling Components across the Plant Kingdom That Communicate Both Pathways
title_full_unstemmed An Overview of PRR- and NLR-Mediated Immunities: Conserved Signaling Components across the Plant Kingdom That Communicate Both Pathways
title_short An Overview of PRR- and NLR-Mediated Immunities: Conserved Signaling Components across the Plant Kingdom That Communicate Both Pathways
title_sort overview of prr- and nlr-mediated immunities: conserved signaling components across the plant kingdom that communicate both pathways
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9654257/
https://www.ncbi.nlm.nih.gov/pubmed/36361764
http://dx.doi.org/10.3390/ijms232112974
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