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Chitin perception in plasmodesmata characterizes submembrane immune-signaling specificity in plants

The plasma membrane (PM) is composed of heterogeneous subdomains, characterized by differences in protein and lipid composition. PM receptors can be dynamically sorted into membrane domains to underpin signaling in response to extracellular stimuli. In plants, the plasmodesmal PM is a discrete micro...

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Autores principales: Cheval, Cécilia, Samwald, Sebastian, Johnston, Matthew G., de Keijzer, Jeroen, Breakspear, Andrew, Liu, Xiaokun, Bellandi, Annalisa, Kadota, Yasuhiro, Zipfel, Cyril, Faulkner, Christine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7196898/
https://www.ncbi.nlm.nih.gov/pubmed/32284410
http://dx.doi.org/10.1073/pnas.1907799117
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author Cheval, Cécilia
Samwald, Sebastian
Johnston, Matthew G.
de Keijzer, Jeroen
Breakspear, Andrew
Liu, Xiaokun
Bellandi, Annalisa
Kadota, Yasuhiro
Zipfel, Cyril
Faulkner, Christine
author_facet Cheval, Cécilia
Samwald, Sebastian
Johnston, Matthew G.
de Keijzer, Jeroen
Breakspear, Andrew
Liu, Xiaokun
Bellandi, Annalisa
Kadota, Yasuhiro
Zipfel, Cyril
Faulkner, Christine
author_sort Cheval, Cécilia
collection PubMed
description The plasma membrane (PM) is composed of heterogeneous subdomains, characterized by differences in protein and lipid composition. PM receptors can be dynamically sorted into membrane domains to underpin signaling in response to extracellular stimuli. In plants, the plasmodesmal PM is a discrete microdomain that hosts specific receptors and responses. We exploited the independence of this PM domain to investigate how membrane domains can independently integrate a signal that triggers responses across the cell. Focusing on chitin signaling, we found that responses in the plasmodesmal PM require the LysM receptor kinases LYK4 and LYK5 in addition to LYM2. Chitin induces dynamic changes in the localization, association, or mobility of these receptors, but only LYM2 and LYK4 are detected in the plasmodesmal PM. We further uncovered that chitin-induced production of reactive oxygen species and callose depends on specific signaling events that lead to plasmodesmata closure. Our results demonstrate that distinct membrane domains can integrate a common signal with specific machinery that initiates discrete signaling cascades to produce a localized response.
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spelling pubmed-71968982020-05-06 Chitin perception in plasmodesmata characterizes submembrane immune-signaling specificity in plants Cheval, Cécilia Samwald, Sebastian Johnston, Matthew G. de Keijzer, Jeroen Breakspear, Andrew Liu, Xiaokun Bellandi, Annalisa Kadota, Yasuhiro Zipfel, Cyril Faulkner, Christine Proc Natl Acad Sci U S A PNAS Plus The plasma membrane (PM) is composed of heterogeneous subdomains, characterized by differences in protein and lipid composition. PM receptors can be dynamically sorted into membrane domains to underpin signaling in response to extracellular stimuli. In plants, the plasmodesmal PM is a discrete microdomain that hosts specific receptors and responses. We exploited the independence of this PM domain to investigate how membrane domains can independently integrate a signal that triggers responses across the cell. Focusing on chitin signaling, we found that responses in the plasmodesmal PM require the LysM receptor kinases LYK4 and LYK5 in addition to LYM2. Chitin induces dynamic changes in the localization, association, or mobility of these receptors, but only LYM2 and LYK4 are detected in the plasmodesmal PM. We further uncovered that chitin-induced production of reactive oxygen species and callose depends on specific signaling events that lead to plasmodesmata closure. Our results demonstrate that distinct membrane domains can integrate a common signal with specific machinery that initiates discrete signaling cascades to produce a localized response. National Academy of Sciences 2020-04-28 2020-04-13 /pmc/articles/PMC7196898/ /pubmed/32284410 http://dx.doi.org/10.1073/pnas.1907799117 Text en Copyright © 2020 the Author(s). Published by PNAS. http://creativecommons.org/licenses/by/4.0/ https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle PNAS Plus
Cheval, Cécilia
Samwald, Sebastian
Johnston, Matthew G.
de Keijzer, Jeroen
Breakspear, Andrew
Liu, Xiaokun
Bellandi, Annalisa
Kadota, Yasuhiro
Zipfel, Cyril
Faulkner, Christine
Chitin perception in plasmodesmata characterizes submembrane immune-signaling specificity in plants
title Chitin perception in plasmodesmata characterizes submembrane immune-signaling specificity in plants
title_full Chitin perception in plasmodesmata characterizes submembrane immune-signaling specificity in plants
title_fullStr Chitin perception in plasmodesmata characterizes submembrane immune-signaling specificity in plants
title_full_unstemmed Chitin perception in plasmodesmata characterizes submembrane immune-signaling specificity in plants
title_short Chitin perception in plasmodesmata characterizes submembrane immune-signaling specificity in plants
title_sort chitin perception in plasmodesmata characterizes submembrane immune-signaling specificity in plants
topic PNAS Plus
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7196898/
https://www.ncbi.nlm.nih.gov/pubmed/32284410
http://dx.doi.org/10.1073/pnas.1907799117
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