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Rapid transporter regulation prevents substrate flow traffic jams in boron transport
Nutrient uptake by roots often involves substrate-dependent regulated nutrient transporters. For robust uptake, the system requires a regulatory circuit within cells and a collective, coordinated behaviour across the tissue. A paradigm for such systems is boron uptake, known for its directional tran...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5621839/ https://www.ncbi.nlm.nih.gov/pubmed/28870285 http://dx.doi.org/10.7554/eLife.27038 |
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author | Sotta, Naoyuki Duncan, Susan Tanaka, Mayuki Sato, Takafumi Marée, Athanasius FM Fujiwara, Toru Grieneisen, Verônica A |
author_facet | Sotta, Naoyuki Duncan, Susan Tanaka, Mayuki Sato, Takafumi Marée, Athanasius FM Fujiwara, Toru Grieneisen, Verônica A |
author_sort | Sotta, Naoyuki |
collection | PubMed |
description | Nutrient uptake by roots often involves substrate-dependent regulated nutrient transporters. For robust uptake, the system requires a regulatory circuit within cells and a collective, coordinated behaviour across the tissue. A paradigm for such systems is boron uptake, known for its directional transport and homeostasis, as boron is essential for plant growth but toxic at high concentrations. In Arabidopsis thaliana, boron uptake occurs via diffusion facilitators (NIPs) and exporters (BORs), each presenting distinct polarity. Intriguingly, although boron soil concentrations are homogenous and stable, both transporters manifest strikingly swift boron-dependent regulation. Through mathematical modelling, we demonstrate that slower regulation of these transporters leads to physiologically detrimental oscillatory behaviour. Cells become periodically exposed to potentially cytotoxic boron levels, and nutrient throughput to the xylem becomes hampered. We conclude that, while maintaining homeostasis, swift transporter regulation within a polarised tissue context is critical to prevent intrinsic traffic-jam like behaviour of nutrient flow. |
format | Online Article Text |
id | pubmed-5621839 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-56218392017-10-02 Rapid transporter regulation prevents substrate flow traffic jams in boron transport Sotta, Naoyuki Duncan, Susan Tanaka, Mayuki Sato, Takafumi Marée, Athanasius FM Fujiwara, Toru Grieneisen, Verônica A eLife Computational and Systems Biology Nutrient uptake by roots often involves substrate-dependent regulated nutrient transporters. For robust uptake, the system requires a regulatory circuit within cells and a collective, coordinated behaviour across the tissue. A paradigm for such systems is boron uptake, known for its directional transport and homeostasis, as boron is essential for plant growth but toxic at high concentrations. In Arabidopsis thaliana, boron uptake occurs via diffusion facilitators (NIPs) and exporters (BORs), each presenting distinct polarity. Intriguingly, although boron soil concentrations are homogenous and stable, both transporters manifest strikingly swift boron-dependent regulation. Through mathematical modelling, we demonstrate that slower regulation of these transporters leads to physiologically detrimental oscillatory behaviour. Cells become periodically exposed to potentially cytotoxic boron levels, and nutrient throughput to the xylem becomes hampered. We conclude that, while maintaining homeostasis, swift transporter regulation within a polarised tissue context is critical to prevent intrinsic traffic-jam like behaviour of nutrient flow. eLife Sciences Publications, Ltd 2017-09-05 /pmc/articles/PMC5621839/ /pubmed/28870285 http://dx.doi.org/10.7554/eLife.27038 Text en © 2017, Sotta et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Computational and Systems Biology Sotta, Naoyuki Duncan, Susan Tanaka, Mayuki Sato, Takafumi Marée, Athanasius FM Fujiwara, Toru Grieneisen, Verônica A Rapid transporter regulation prevents substrate flow traffic jams in boron transport |
title | Rapid transporter regulation prevents substrate flow traffic jams in boron transport |
title_full | Rapid transporter regulation prevents substrate flow traffic jams in boron transport |
title_fullStr | Rapid transporter regulation prevents substrate flow traffic jams in boron transport |
title_full_unstemmed | Rapid transporter regulation prevents substrate flow traffic jams in boron transport |
title_short | Rapid transporter regulation prevents substrate flow traffic jams in boron transport |
title_sort | rapid transporter regulation prevents substrate flow traffic jams in boron transport |
topic | Computational and Systems Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5621839/ https://www.ncbi.nlm.nih.gov/pubmed/28870285 http://dx.doi.org/10.7554/eLife.27038 |
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