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Modeling halotropism: a key role for root tip architecture and reflux loop remodeling in redistributing auxin

A key characteristic of plant development is its plasticity in response to various and dynamically changing environmental conditions. Tropisms contribute to this flexibility by allowing plant organs to grow from or towards environmental cues. Halotropism is a recently described tropism in which plan...

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Autores principales: van den Berg, Thea, Korver, Ruud A., Testerink, Christa, ten Tusscher, Kirsten H. W. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5047658/
https://www.ncbi.nlm.nih.gov/pubmed/27510970
http://dx.doi.org/10.1242/dev.135111
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author van den Berg, Thea
Korver, Ruud A.
Testerink, Christa
ten Tusscher, Kirsten H. W. J.
author_facet van den Berg, Thea
Korver, Ruud A.
Testerink, Christa
ten Tusscher, Kirsten H. W. J.
author_sort van den Berg, Thea
collection PubMed
description A key characteristic of plant development is its plasticity in response to various and dynamically changing environmental conditions. Tropisms contribute to this flexibility by allowing plant organs to grow from or towards environmental cues. Halotropism is a recently described tropism in which plant roots bend away from salt. During halotropism, as in most other tropisms, directional growth is generated through an asymmetric auxin distribution that generates differences in growth rate and hence induces bending. Here, we develop a detailed model of auxin transport in the Arabidopsis root tip and combine this with experiments to investigate the processes generating auxin asymmetry during halotropism. Our model points to the key role of root tip architecture in allowing the decrease in PIN2 at the salt-exposed side of the root to result in a re-routing of auxin to the opposite side. In addition, our model demonstrates how feedback of auxin on the auxin transporter AUX1 amplifies this auxin asymmetry, while a salt-induced transient increase in PIN1 levels increases the speed at which this occurs. Using AUX1-GFP imaging and pin1 mutants, we experimentally confirmed these model predictions, thus expanding our knowledge of the cellular basis of halotropism.
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spelling pubmed-50476582016-10-06 Modeling halotropism: a key role for root tip architecture and reflux loop remodeling in redistributing auxin van den Berg, Thea Korver, Ruud A. Testerink, Christa ten Tusscher, Kirsten H. W. J. Development Research Article A key characteristic of plant development is its plasticity in response to various and dynamically changing environmental conditions. Tropisms contribute to this flexibility by allowing plant organs to grow from or towards environmental cues. Halotropism is a recently described tropism in which plant roots bend away from salt. During halotropism, as in most other tropisms, directional growth is generated through an asymmetric auxin distribution that generates differences in growth rate and hence induces bending. Here, we develop a detailed model of auxin transport in the Arabidopsis root tip and combine this with experiments to investigate the processes generating auxin asymmetry during halotropism. Our model points to the key role of root tip architecture in allowing the decrease in PIN2 at the salt-exposed side of the root to result in a re-routing of auxin to the opposite side. In addition, our model demonstrates how feedback of auxin on the auxin transporter AUX1 amplifies this auxin asymmetry, while a salt-induced transient increase in PIN1 levels increases the speed at which this occurs. Using AUX1-GFP imaging and pin1 mutants, we experimentally confirmed these model predictions, thus expanding our knowledge of the cellular basis of halotropism. The Company of Biologists Ltd 2016-09-15 /pmc/articles/PMC5047658/ /pubmed/27510970 http://dx.doi.org/10.1242/dev.135111 Text en © 2016. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
van den Berg, Thea
Korver, Ruud A.
Testerink, Christa
ten Tusscher, Kirsten H. W. J.
Modeling halotropism: a key role for root tip architecture and reflux loop remodeling in redistributing auxin
title Modeling halotropism: a key role for root tip architecture and reflux loop remodeling in redistributing auxin
title_full Modeling halotropism: a key role for root tip architecture and reflux loop remodeling in redistributing auxin
title_fullStr Modeling halotropism: a key role for root tip architecture and reflux loop remodeling in redistributing auxin
title_full_unstemmed Modeling halotropism: a key role for root tip architecture and reflux loop remodeling in redistributing auxin
title_short Modeling halotropism: a key role for root tip architecture and reflux loop remodeling in redistributing auxin
title_sort modeling halotropism: a key role for root tip architecture and reflux loop remodeling in redistributing auxin
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5047658/
https://www.ncbi.nlm.nih.gov/pubmed/27510970
http://dx.doi.org/10.1242/dev.135111
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