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Mechanodetection of neighbor plants elicits adaptive leaf movements through calcium dynamics
Plants detect their neighbors via various cues, including reflected light and touching of leaf tips, which elicit upward leaf movement (hyponasty). It is currently unknown how touch is sensed and how the signal is transferred from the leaf tip to the petiole base that drives hyponasty. Here, we show...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10511701/ https://www.ncbi.nlm.nih.gov/pubmed/37730832 http://dx.doi.org/10.1038/s41467-023-41530-0 |
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author | Pantazopoulou, Chrysoula K. Buti, Sara Nguyen, Chi Tam Oskam, Lisa Weits, Daan A. Farmer, Edward E. Kajala, Kaisa Pierik, Ronald |
author_facet | Pantazopoulou, Chrysoula K. Buti, Sara Nguyen, Chi Tam Oskam, Lisa Weits, Daan A. Farmer, Edward E. Kajala, Kaisa Pierik, Ronald |
author_sort | Pantazopoulou, Chrysoula K. |
collection | PubMed |
description | Plants detect their neighbors via various cues, including reflected light and touching of leaf tips, which elicit upward leaf movement (hyponasty). It is currently unknown how touch is sensed and how the signal is transferred from the leaf tip to the petiole base that drives hyponasty. Here, we show that touch-induced hyponasty involves a signal transduction pathway that is distinct from light-mediated hyponasty. We found that mechanostimulation of the leaf tip upon touching causes cytosolic calcium ([Ca(2+)](cyt) induction in leaf tip trichomes that spreads towards the petiole. Both perturbation of the calcium response and the absence of trichomes reduce touch-induced hyponasty. Finally, using plant competition assays, we show that touch-induced hyponasty is adaptive in dense stands of Arabidopsis. We thus establish a novel, adaptive mechanism regulating hyponastic leaf movement in response to mechanostimulation by neighbors in dense vegetation. |
format | Online Article Text |
id | pubmed-10511701 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-105117012023-09-22 Mechanodetection of neighbor plants elicits adaptive leaf movements through calcium dynamics Pantazopoulou, Chrysoula K. Buti, Sara Nguyen, Chi Tam Oskam, Lisa Weits, Daan A. Farmer, Edward E. Kajala, Kaisa Pierik, Ronald Nat Commun Article Plants detect their neighbors via various cues, including reflected light and touching of leaf tips, which elicit upward leaf movement (hyponasty). It is currently unknown how touch is sensed and how the signal is transferred from the leaf tip to the petiole base that drives hyponasty. Here, we show that touch-induced hyponasty involves a signal transduction pathway that is distinct from light-mediated hyponasty. We found that mechanostimulation of the leaf tip upon touching causes cytosolic calcium ([Ca(2+)](cyt) induction in leaf tip trichomes that spreads towards the petiole. Both perturbation of the calcium response and the absence of trichomes reduce touch-induced hyponasty. Finally, using plant competition assays, we show that touch-induced hyponasty is adaptive in dense stands of Arabidopsis. We thus establish a novel, adaptive mechanism regulating hyponastic leaf movement in response to mechanostimulation by neighbors in dense vegetation. Nature Publishing Group UK 2023-09-20 /pmc/articles/PMC10511701/ /pubmed/37730832 http://dx.doi.org/10.1038/s41467-023-41530-0 Text en © The Author(s) 2023 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Pantazopoulou, Chrysoula K. Buti, Sara Nguyen, Chi Tam Oskam, Lisa Weits, Daan A. Farmer, Edward E. Kajala, Kaisa Pierik, Ronald Mechanodetection of neighbor plants elicits adaptive leaf movements through calcium dynamics |
title | Mechanodetection of neighbor plants elicits adaptive leaf movements through calcium dynamics |
title_full | Mechanodetection of neighbor plants elicits adaptive leaf movements through calcium dynamics |
title_fullStr | Mechanodetection of neighbor plants elicits adaptive leaf movements through calcium dynamics |
title_full_unstemmed | Mechanodetection of neighbor plants elicits adaptive leaf movements through calcium dynamics |
title_short | Mechanodetection of neighbor plants elicits adaptive leaf movements through calcium dynamics |
title_sort | mechanodetection of neighbor plants elicits adaptive leaf movements through calcium dynamics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10511701/ https://www.ncbi.nlm.nih.gov/pubmed/37730832 http://dx.doi.org/10.1038/s41467-023-41530-0 |
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