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A Rho-based reaction-diffusion system governs cell wall patterning in metaxylem vessels

Rho GTPases play crucial roles in cell polarity and pattern formation. ROPs, Rho of plant GTPases, are widely involved in cell wall patterning in plants, yet the molecular mechanism underlying their action remains unknown. Arabidopsis ROP11 is locally activated to form plasma membrane domains, which...

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Autores principales: Nagashima, Yoshinobu, Tsugawa, Satoru, Mochizuki, Atsushi, Sasaki, Takema, Fukuda, Hiroo, Oda, Yoshihisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6070580/
https://www.ncbi.nlm.nih.gov/pubmed/30069009
http://dx.doi.org/10.1038/s41598-018-29543-y
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author Nagashima, Yoshinobu
Tsugawa, Satoru
Mochizuki, Atsushi
Sasaki, Takema
Fukuda, Hiroo
Oda, Yoshihisa
author_facet Nagashima, Yoshinobu
Tsugawa, Satoru
Mochizuki, Atsushi
Sasaki, Takema
Fukuda, Hiroo
Oda, Yoshihisa
author_sort Nagashima, Yoshinobu
collection PubMed
description Rho GTPases play crucial roles in cell polarity and pattern formation. ROPs, Rho of plant GTPases, are widely involved in cell wall patterning in plants, yet the molecular mechanism underlying their action remains unknown. Arabidopsis ROP11 is locally activated to form plasma membrane domains, which direct formation of cell wall pits in metaxylem vessel cells through interaction with cortical microtubules. Here, we show that the pattern formation of cell wall pits is governed by ROP activation via a reaction-diffusion mechanism. Genetic analysis and reconstructive assays revealed that ROPGEF4/7 and ROPGAP3/4, which encode ROP activators and inactivators, respectively, regulated the formation of ROP-activated domains; these in turn determined the pattern of cell wall pits. Mathematical modelling showed that ROP-activation cycle generated ROP domains by reaction-diffusion mechanism. The model predicted that a positive feedback and slow diffusion of ROP11-ROPGEF4 complex were required to generate ROP-activated domains. ROPGEF4 formed a dimer that interacted with activated ROP11 in vivo, which could provide positive feedback for ROP activation. ROPGEF4 was highly stable on the plasma membrane and inhibited ROP11 diffusion. Our study indicated that ROP-based reaction-diffusion system self-organizes ROP-activated domains, thereby determines the pit pattern of metaxylem vessels.
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spelling pubmed-60705802018-08-06 A Rho-based reaction-diffusion system governs cell wall patterning in metaxylem vessels Nagashima, Yoshinobu Tsugawa, Satoru Mochizuki, Atsushi Sasaki, Takema Fukuda, Hiroo Oda, Yoshihisa Sci Rep Article Rho GTPases play crucial roles in cell polarity and pattern formation. ROPs, Rho of plant GTPases, are widely involved in cell wall patterning in plants, yet the molecular mechanism underlying their action remains unknown. Arabidopsis ROP11 is locally activated to form plasma membrane domains, which direct formation of cell wall pits in metaxylem vessel cells through interaction with cortical microtubules. Here, we show that the pattern formation of cell wall pits is governed by ROP activation via a reaction-diffusion mechanism. Genetic analysis and reconstructive assays revealed that ROPGEF4/7 and ROPGAP3/4, which encode ROP activators and inactivators, respectively, regulated the formation of ROP-activated domains; these in turn determined the pattern of cell wall pits. Mathematical modelling showed that ROP-activation cycle generated ROP domains by reaction-diffusion mechanism. The model predicted that a positive feedback and slow diffusion of ROP11-ROPGEF4 complex were required to generate ROP-activated domains. ROPGEF4 formed a dimer that interacted with activated ROP11 in vivo, which could provide positive feedback for ROP activation. ROPGEF4 was highly stable on the plasma membrane and inhibited ROP11 diffusion. Our study indicated that ROP-based reaction-diffusion system self-organizes ROP-activated domains, thereby determines the pit pattern of metaxylem vessels. Nature Publishing Group UK 2018-08-01 /pmc/articles/PMC6070580/ /pubmed/30069009 http://dx.doi.org/10.1038/s41598-018-29543-y Text en © The Author(s) 2018 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/.
spellingShingle Article
Nagashima, Yoshinobu
Tsugawa, Satoru
Mochizuki, Atsushi
Sasaki, Takema
Fukuda, Hiroo
Oda, Yoshihisa
A Rho-based reaction-diffusion system governs cell wall patterning in metaxylem vessels
title A Rho-based reaction-diffusion system governs cell wall patterning in metaxylem vessels
title_full A Rho-based reaction-diffusion system governs cell wall patterning in metaxylem vessels
title_fullStr A Rho-based reaction-diffusion system governs cell wall patterning in metaxylem vessels
title_full_unstemmed A Rho-based reaction-diffusion system governs cell wall patterning in metaxylem vessels
title_short A Rho-based reaction-diffusion system governs cell wall patterning in metaxylem vessels
title_sort rho-based reaction-diffusion system governs cell wall patterning in metaxylem vessels
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6070580/
https://www.ncbi.nlm.nih.gov/pubmed/30069009
http://dx.doi.org/10.1038/s41598-018-29543-y
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