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RGI‐GOLVEN signaling promotes cell surface immune receptor abundance to regulate plant immunity

Plant immune responses must be tightly controlled for proper allocation of resources for growth and development. In plants, endogenous signaling peptides regulate developmental and growth‐related processes. Recent research indicates that some of these peptides also have regulatory functions in the c...

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Autores principales: Stegmann, Martin, Zecua‐Ramirez, Patricia, Ludwig, Christina, Lee, Ho‐Seok, Peterson, Brenda, Nimchuk, Zachary L, Belkhadir, Youssef, Hückelhoven, Ralph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9066070/
https://www.ncbi.nlm.nih.gov/pubmed/35229426
http://dx.doi.org/10.15252/embr.202153281
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author Stegmann, Martin
Zecua‐Ramirez, Patricia
Ludwig, Christina
Lee, Ho‐Seok
Peterson, Brenda
Nimchuk, Zachary L
Belkhadir, Youssef
Hückelhoven, Ralph
author_facet Stegmann, Martin
Zecua‐Ramirez, Patricia
Ludwig, Christina
Lee, Ho‐Seok
Peterson, Brenda
Nimchuk, Zachary L
Belkhadir, Youssef
Hückelhoven, Ralph
author_sort Stegmann, Martin
collection PubMed
description Plant immune responses must be tightly controlled for proper allocation of resources for growth and development. In plants, endogenous signaling peptides regulate developmental and growth‐related processes. Recent research indicates that some of these peptides also have regulatory functions in the control of plant immune responses. This classifies these peptides as phytocytokines as they show analogies with metazoan cytokines. However, the mechanistic basis for phytocytokine‐mediated regulation of plant immunity remains largely elusive. Here, we identify GOLVEN2 (GLV2) peptides as phytocytokines in Arabidopsis thaliana. GLV2 signaling enhances sensitivity of plants to elicitation with immunogenic bacterial elicitors and contributes to resistance against virulent bacterial pathogens. GLV2 is perceived by ROOT MERISTEM GROWTH FACTOR 1 INSENSITIVE (RGI) receptors. RGI mutants show reduced elicitor sensitivity and enhanced susceptibility to bacterial infection. RGI3 forms ligand‐induced complexes with the pattern recognition receptor (PRR) FLAGELLIN SENSITIVE 2 (FLS2), suggesting that RGIs are part of PRR signaling platforms. GLV2‐RGI signaling promotes PRR abundance independent of transcriptional regulation and controls plant immunity via a previously undescribed mechanism of phytocytokine activity.
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spelling pubmed-90660702022-05-04 RGI‐GOLVEN signaling promotes cell surface immune receptor abundance to regulate plant immunity Stegmann, Martin Zecua‐Ramirez, Patricia Ludwig, Christina Lee, Ho‐Seok Peterson, Brenda Nimchuk, Zachary L Belkhadir, Youssef Hückelhoven, Ralph EMBO Rep Articles Plant immune responses must be tightly controlled for proper allocation of resources for growth and development. In plants, endogenous signaling peptides regulate developmental and growth‐related processes. Recent research indicates that some of these peptides also have regulatory functions in the control of plant immune responses. This classifies these peptides as phytocytokines as they show analogies with metazoan cytokines. However, the mechanistic basis for phytocytokine‐mediated regulation of plant immunity remains largely elusive. Here, we identify GOLVEN2 (GLV2) peptides as phytocytokines in Arabidopsis thaliana. GLV2 signaling enhances sensitivity of plants to elicitation with immunogenic bacterial elicitors and contributes to resistance against virulent bacterial pathogens. GLV2 is perceived by ROOT MERISTEM GROWTH FACTOR 1 INSENSITIVE (RGI) receptors. RGI mutants show reduced elicitor sensitivity and enhanced susceptibility to bacterial infection. RGI3 forms ligand‐induced complexes with the pattern recognition receptor (PRR) FLAGELLIN SENSITIVE 2 (FLS2), suggesting that RGIs are part of PRR signaling platforms. GLV2‐RGI signaling promotes PRR abundance independent of transcriptional regulation and controls plant immunity via a previously undescribed mechanism of phytocytokine activity. John Wiley and Sons Inc. 2022-03-01 /pmc/articles/PMC9066070/ /pubmed/35229426 http://dx.doi.org/10.15252/embr.202153281 Text en © 2022 The Authors. Published under the terms of the CC BY 4.0 license https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Stegmann, Martin
Zecua‐Ramirez, Patricia
Ludwig, Christina
Lee, Ho‐Seok
Peterson, Brenda
Nimchuk, Zachary L
Belkhadir, Youssef
Hückelhoven, Ralph
RGI‐GOLVEN signaling promotes cell surface immune receptor abundance to regulate plant immunity
title RGI‐GOLVEN signaling promotes cell surface immune receptor abundance to regulate plant immunity
title_full RGI‐GOLVEN signaling promotes cell surface immune receptor abundance to regulate plant immunity
title_fullStr RGI‐GOLVEN signaling promotes cell surface immune receptor abundance to regulate plant immunity
title_full_unstemmed RGI‐GOLVEN signaling promotes cell surface immune receptor abundance to regulate plant immunity
title_short RGI‐GOLVEN signaling promotes cell surface immune receptor abundance to regulate plant immunity
title_sort rgi‐golven signaling promotes cell surface immune receptor abundance to regulate plant immunity
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9066070/
https://www.ncbi.nlm.nih.gov/pubmed/35229426
http://dx.doi.org/10.15252/embr.202153281
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