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Dissecting the membrane-microtubule sensor in grapevine defence

Specific populations of plant microtubules cooperate with the plasma membrane to sense and process abiotic stress signals, such as cold stress. The current study derived from the question, to what extent this perception system is active in biotic stress signalling. The experimental system consisted...

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Autores principales: Guan, Pingyin, Shi, Wenjing, Riemann, Michael, Nick, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8632924/
https://www.ncbi.nlm.nih.gov/pubmed/34848701
http://dx.doi.org/10.1038/s41438-021-00703-y
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author Guan, Pingyin
Shi, Wenjing
Riemann, Michael
Nick, Peter
author_facet Guan, Pingyin
Shi, Wenjing
Riemann, Michael
Nick, Peter
author_sort Guan, Pingyin
collection PubMed
description Specific populations of plant microtubules cooperate with the plasma membrane to sense and process abiotic stress signals, such as cold stress. The current study derived from the question, to what extent this perception system is active in biotic stress signalling. The experimental system consisted of grapevine cell lines, where microtubules or actin filaments are visualised by GFP, such that their response became visible in vivo. We used the bacterial elicitors harpin (inducing cell-death related defence), or flg22 (inducing basal immunity) in combination with modulators of membrane fluidity, or microtubules. We show that DMSO, a membrane rigidifier, can cause microtubule bundling and trigger defence responses, including activation of phytoalexin transcripts. However, DMSO inhibited the gene expression in response to harpin, while promoting the gene expression in response to flg22. Treatment with DMSO also rendered microtubules more persistent to harpin. Paradoxically, Benzylalcohol (BA), a membrane fluidiser, acted in the same way as DMSO. Neither GdCl(3), nor diphenylene iodonium were able to block the inhibitory effect of membrane rigidification on harpin-induced gene expression. Treatment with taxol stabilised microtubule against harpin but amplified the response of PAL transcripts. Therefore, the data support implications of a model that deploys specific responses to pathogen-derived signals.
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spelling pubmed-86329242021-12-01 Dissecting the membrane-microtubule sensor in grapevine defence Guan, Pingyin Shi, Wenjing Riemann, Michael Nick, Peter Hortic Res Article Specific populations of plant microtubules cooperate with the plasma membrane to sense and process abiotic stress signals, such as cold stress. The current study derived from the question, to what extent this perception system is active in biotic stress signalling. The experimental system consisted of grapevine cell lines, where microtubules or actin filaments are visualised by GFP, such that their response became visible in vivo. We used the bacterial elicitors harpin (inducing cell-death related defence), or flg22 (inducing basal immunity) in combination with modulators of membrane fluidity, or microtubules. We show that DMSO, a membrane rigidifier, can cause microtubule bundling and trigger defence responses, including activation of phytoalexin transcripts. However, DMSO inhibited the gene expression in response to harpin, while promoting the gene expression in response to flg22. Treatment with DMSO also rendered microtubules more persistent to harpin. Paradoxically, Benzylalcohol (BA), a membrane fluidiser, acted in the same way as DMSO. Neither GdCl(3), nor diphenylene iodonium were able to block the inhibitory effect of membrane rigidification on harpin-induced gene expression. Treatment with taxol stabilised microtubule against harpin but amplified the response of PAL transcripts. Therefore, the data support implications of a model that deploys specific responses to pathogen-derived signals. Nature Publishing Group UK 2021-12-01 /pmc/articles/PMC8632924/ /pubmed/34848701 http://dx.doi.org/10.1038/s41438-021-00703-y Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Guan, Pingyin
Shi, Wenjing
Riemann, Michael
Nick, Peter
Dissecting the membrane-microtubule sensor in grapevine defence
title Dissecting the membrane-microtubule sensor in grapevine defence
title_full Dissecting the membrane-microtubule sensor in grapevine defence
title_fullStr Dissecting the membrane-microtubule sensor in grapevine defence
title_full_unstemmed Dissecting the membrane-microtubule sensor in grapevine defence
title_short Dissecting the membrane-microtubule sensor in grapevine defence
title_sort dissecting the membrane-microtubule sensor in grapevine defence
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8632924/
https://www.ncbi.nlm.nih.gov/pubmed/34848701
http://dx.doi.org/10.1038/s41438-021-00703-y
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