SEC14-like condensate phase transitions at plasma membranes regulate root growth in Arabidopsis.

Protein function can be modulated by phase transitions in their material properties, which can range from liquid- to solid-like; yet, the mechanisms that drive these transitions and whether they are important for physiology are still unknown. In the model plant Arabidopsis, we show that developmenta...

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Main Authors: Chen Liu, Andriani Mentzelopoulou, Fotini Papagavriil, Prashanth Ramachandran, Artemis Perraki, Lucas Claus, Sebastian Barg, Peter Dörmann, Yvon Jaillais, Philipp Johnen, Eugenia Russinova, Electra Gizeli, Gabriel Schaaf, Panagiotis Nikolaou Moschou
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2023-09-01
Series:PLoS Biology
Online Access:https://journals.plos.org/plosbiology/article/file?id=10.1371/journal.pbio.3002305&type=printable
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author Chen Liu
Andriani Mentzelopoulou
Fotini Papagavriil
Prashanth Ramachandran
Artemis Perraki
Lucas Claus
Sebastian Barg
Peter Dörmann
Yvon Jaillais
Philipp Johnen
Eugenia Russinova
Electra Gizeli
Gabriel Schaaf
Panagiotis Nikolaou Moschou
author_facet Chen Liu
Andriani Mentzelopoulou
Fotini Papagavriil
Prashanth Ramachandran
Artemis Perraki
Lucas Claus
Sebastian Barg
Peter Dörmann
Yvon Jaillais
Philipp Johnen
Eugenia Russinova
Electra Gizeli
Gabriel Schaaf
Panagiotis Nikolaou Moschou
author_sort Chen Liu
collection DOAJ
description Protein function can be modulated by phase transitions in their material properties, which can range from liquid- to solid-like; yet, the mechanisms that drive these transitions and whether they are important for physiology are still unknown. In the model plant Arabidopsis, we show that developmental robustness is reinforced by phase transitions of the plasma membrane-bound lipid-binding protein SEC14-like. Using imaging, genetics, and in vitro reconstitution experiments, we show that SEC14-like undergoes liquid-like phase separation in the root stem cells. Outside the stem cell niche, SEC14-like associates with the caspase-like protease separase and conserved microtubule motors at unique polar plasma membrane interfaces. In these interfaces, SEC14-like undergoes processing by separase, which promotes its liquid-to-solid transition. This transition is important for root development, as lines expressing an uncleavable SEC14-like variant or mutants of separase and associated microtubule motors show similar developmental phenotypes. Furthermore, the processed and solidified but not the liquid form of SEC14-like interacts with and regulates the polarity of the auxin efflux carrier PINFORMED2. This work demonstrates that robust development can involve liquid-to-solid transitions mediated by proteolysis at unique plasma membrane interfaces.
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spelling doaj.art-e2a44caa675b4120a3b674204b069a272023-10-04T05:30:53ZengPublic Library of Science (PLoS)PLoS Biology1544-91731545-78852023-09-01219e300230510.1371/journal.pbio.3002305SEC14-like condensate phase transitions at plasma membranes regulate root growth in Arabidopsis.Chen LiuAndriani MentzelopoulouFotini PapagavriilPrashanth RamachandranArtemis PerrakiLucas ClausSebastian BargPeter DörmannYvon JaillaisPhilipp JohnenEugenia RussinovaElectra GizeliGabriel SchaafPanagiotis Nikolaou MoschouProtein function can be modulated by phase transitions in their material properties, which can range from liquid- to solid-like; yet, the mechanisms that drive these transitions and whether they are important for physiology are still unknown. In the model plant Arabidopsis, we show that developmental robustness is reinforced by phase transitions of the plasma membrane-bound lipid-binding protein SEC14-like. Using imaging, genetics, and in vitro reconstitution experiments, we show that SEC14-like undergoes liquid-like phase separation in the root stem cells. Outside the stem cell niche, SEC14-like associates with the caspase-like protease separase and conserved microtubule motors at unique polar plasma membrane interfaces. In these interfaces, SEC14-like undergoes processing by separase, which promotes its liquid-to-solid transition. This transition is important for root development, as lines expressing an uncleavable SEC14-like variant or mutants of separase and associated microtubule motors show similar developmental phenotypes. Furthermore, the processed and solidified but not the liquid form of SEC14-like interacts with and regulates the polarity of the auxin efflux carrier PINFORMED2. This work demonstrates that robust development can involve liquid-to-solid transitions mediated by proteolysis at unique plasma membrane interfaces.https://journals.plos.org/plosbiology/article/file?id=10.1371/journal.pbio.3002305&type=printable
spellingShingle Chen Liu
Andriani Mentzelopoulou
Fotini Papagavriil
Prashanth Ramachandran
Artemis Perraki
Lucas Claus
Sebastian Barg
Peter Dörmann
Yvon Jaillais
Philipp Johnen
Eugenia Russinova
Electra Gizeli
Gabriel Schaaf
Panagiotis Nikolaou Moschou
SEC14-like condensate phase transitions at plasma membranes regulate root growth in Arabidopsis.
PLoS Biology
title SEC14-like condensate phase transitions at plasma membranes regulate root growth in Arabidopsis.
title_full SEC14-like condensate phase transitions at plasma membranes regulate root growth in Arabidopsis.
title_fullStr SEC14-like condensate phase transitions at plasma membranes regulate root growth in Arabidopsis.
title_full_unstemmed SEC14-like condensate phase transitions at plasma membranes regulate root growth in Arabidopsis.
title_short SEC14-like condensate phase transitions at plasma membranes regulate root growth in Arabidopsis.
title_sort sec14 like condensate phase transitions at plasma membranes regulate root growth in arabidopsis
url https://journals.plos.org/plosbiology/article/file?id=10.1371/journal.pbio.3002305&type=printable
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