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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2020
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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. |
format | Online Article Text |
id | pubmed-7196898 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
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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