A Plasma Membrane Nanodomain Ensures Signal Specificity during Osmotic Signaling in Plants

In the course of their growth and development, plants have to constantly perceive and react to their environment. This is achieved in cells by the coordination of complex combinatorial signaling networks. However, how signal integration and specificity are achieved in this context is unknown. With a...

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Veröffentlicht in:Current biology 2020-12, Vol.30 (23), p.4654-4664.e4
Hauptverfasser: Smokvarska, Marija, Francis, Charbel, Platre, Matthieu Pierre, Fiche, Jean-Bernard, Alcon, Carine, Dumont, Xavier, Nacry, Philippe, Bayle, Vincent, Nollmann, Marcelo, Maurel, Christophe, Jaillais, Y., Martiniere, Alexandre
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container_end_page 4664.e4
container_issue 23
container_start_page 4654
container_title Current biology
container_volume 30
creator Smokvarska, Marija
Francis, Charbel
Platre, Matthieu Pierre
Fiche, Jean-Bernard
Alcon, Carine
Dumont, Xavier
Nacry, Philippe
Bayle, Vincent
Nollmann, Marcelo
Maurel, Christophe
Jaillais, Y.
Martiniere, Alexandre
description In the course of their growth and development, plants have to constantly perceive and react to their environment. This is achieved in cells by the coordination of complex combinatorial signaling networks. However, how signal integration and specificity are achieved in this context is unknown. With a focus on the hyperosmotic stimulus, we use live super-resolution light imaging methods to demonstrate that a Rho GTPase, Rho-of-Plant 6 (ROP6), forms stimuli-dependent nanodomains within the plasma membrane (PM). These nanodomains are necessary and sufficient to transduce production of reactive oxygen species (ROS) that act as secondary messengers and trigger several plant adaptive responses to osmotic constraints. Furthermore, osmotic signal triggers interaction between ROP6 and two NADPH oxidases that subsequently generate ROS. ROP6 nanoclustering is also needed for cell surface auxin signaling, but short-time auxin treatment does not induce ROS accumulation. We show that auxin-induced ROP6 nanodomains, unlike osmotically driven ROP6 clusters, do not recruit the NADPH oxidase, RBOHD. Together, our results suggest that Rho GTPase nano-partitioning at the PM ensures signal specificity downstream of independent stimuli. [Display omitted] •An isoform of ROP GTPase mediates ROS signaling and plant responses to osmotic signaling•Osmotic signaling induce nanodomains that contain activated ROP6•Interaction of ROP6 with RBOHs enriches nanodomains locally•Auxin induced nanodomains containing ROP6, but not RBOHs The mechanisms by which plants perceive and transduce osmotic signal remains incompletely understood. Here, Smokvarska et al. find that ROP6 forms nanodomain in response to osmotic signal. Then, ROP6 nanodomain recruits osmotic specific effectors that ensure downstream signal specificity.
doi_str_mv 10.1016/j.cub.2020.09.013
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This is achieved in cells by the coordination of complex combinatorial signaling networks. However, how signal integration and specificity are achieved in this context is unknown. With a focus on the hyperosmotic stimulus, we use live super-resolution light imaging methods to demonstrate that a Rho GTPase, Rho-of-Plant 6 (ROP6), forms stimuli-dependent nanodomains within the plasma membrane (PM). These nanodomains are necessary and sufficient to transduce production of reactive oxygen species (ROS) that act as secondary messengers and trigger several plant adaptive responses to osmotic constraints. Furthermore, osmotic signal triggers interaction between ROP6 and two NADPH oxidases that subsequently generate ROS. ROP6 nanoclustering is also needed for cell surface auxin signaling, but short-time auxin treatment does not induce ROS accumulation. We show that auxin-induced ROP6 nanodomains, unlike osmotically driven ROP6 clusters, do not recruit the NADPH oxidase, RBOHD. 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source Cell Press Free Archives; Elsevier ScienceDirect Journals; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects GTPase
Life Sciences
nanodomain
osmotic
ROP
ROS
signaling
sptPALM
super resolution
Vegetal Biology
title A Plasma Membrane Nanodomain Ensures Signal Specificity during Osmotic Signaling in Plants
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