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Emergence of tissue polarization from synergy of intracellular and extracellular auxin signaling
Plant development is exceptionally flexible as manifested by its potential for organogenesis and regeneration, which are processes involving rearrangements of tissue polarities. Fundamental questions concern how individual cells can polarize in a coordinated manner to integrate into the multicellula...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
European Molecular Biology Organization
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3018162/ https://www.ncbi.nlm.nih.gov/pubmed/21179019 http://dx.doi.org/10.1038/msb.2010.103 |
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author | Wabnik, Krzysztof Kleine-Vehn, Jürgen Balla, Jozef Sauer, Michael Naramoto, Satoshi Reinöhl, Vilém Merks, Roeland M H Govaerts, Willy Friml, Jiří |
author_facet | Wabnik, Krzysztof Kleine-Vehn, Jürgen Balla, Jozef Sauer, Michael Naramoto, Satoshi Reinöhl, Vilém Merks, Roeland M H Govaerts, Willy Friml, Jiří |
author_sort | Wabnik, Krzysztof |
collection | PubMed |
description | Plant development is exceptionally flexible as manifested by its potential for organogenesis and regeneration, which are processes involving rearrangements of tissue polarities. Fundamental questions concern how individual cells can polarize in a coordinated manner to integrate into the multicellular context. In canalization models, the signaling molecule auxin acts as a polarizing cue, and feedback on the intercellular auxin flow is key for synchronized polarity rearrangements. We provide a novel mechanistic framework for canalization, based on up-to-date experimental data and minimal, biologically plausible assumptions. Our model combines the intracellular auxin signaling for expression of PINFORMED (PIN) auxin transporters and the theoretical postulation of extracellular auxin signaling for modulation of PIN subcellular dynamics. Computer simulations faithfully and robustly recapitulated the experimentally observed patterns of tissue polarity and asymmetric auxin distribution during formation and regeneration of vascular systems and during the competitive regulation of shoot branching by apical dominance. Additionally, our model generated new predictions that could be experimentally validated, highlighting a mechanistically conceivable explanation for the PIN polarization and canalization of the auxin flow in plants. |
format | Text |
id | pubmed-3018162 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | European Molecular Biology Organization |
record_format | MEDLINE/PubMed |
spelling | pubmed-30181622011-01-10 Emergence of tissue polarization from synergy of intracellular and extracellular auxin signaling Wabnik, Krzysztof Kleine-Vehn, Jürgen Balla, Jozef Sauer, Michael Naramoto, Satoshi Reinöhl, Vilém Merks, Roeland M H Govaerts, Willy Friml, Jiří Mol Syst Biol Article Plant development is exceptionally flexible as manifested by its potential for organogenesis and regeneration, which are processes involving rearrangements of tissue polarities. Fundamental questions concern how individual cells can polarize in a coordinated manner to integrate into the multicellular context. In canalization models, the signaling molecule auxin acts as a polarizing cue, and feedback on the intercellular auxin flow is key for synchronized polarity rearrangements. We provide a novel mechanistic framework for canalization, based on up-to-date experimental data and minimal, biologically plausible assumptions. Our model combines the intracellular auxin signaling for expression of PINFORMED (PIN) auxin transporters and the theoretical postulation of extracellular auxin signaling for modulation of PIN subcellular dynamics. Computer simulations faithfully and robustly recapitulated the experimentally observed patterns of tissue polarity and asymmetric auxin distribution during formation and regeneration of vascular systems and during the competitive regulation of shoot branching by apical dominance. Additionally, our model generated new predictions that could be experimentally validated, highlighting a mechanistically conceivable explanation for the PIN polarization and canalization of the auxin flow in plants. European Molecular Biology Organization 2010-12-21 /pmc/articles/PMC3018162/ /pubmed/21179019 http://dx.doi.org/10.1038/msb.2010.103 Text en Copyright © 2010, EMBO and Macmillan Publishers Limited https://creativecommons.org/licenses/by-nc-nd/3.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Noncommercial No Derivative Works 3.0 Unported License, which permits distribution and reproduction in any medium, provided the original author and source are credited. This license does not permit commercial exploitation or the creation of derivative works without specific permission. |
spellingShingle | Article Wabnik, Krzysztof Kleine-Vehn, Jürgen Balla, Jozef Sauer, Michael Naramoto, Satoshi Reinöhl, Vilém Merks, Roeland M H Govaerts, Willy Friml, Jiří Emergence of tissue polarization from synergy of intracellular and extracellular auxin signaling |
title | Emergence of tissue polarization from synergy of intracellular and extracellular auxin signaling |
title_full | Emergence of tissue polarization from synergy of intracellular and extracellular auxin signaling |
title_fullStr | Emergence of tissue polarization from synergy of intracellular and extracellular auxin signaling |
title_full_unstemmed | Emergence of tissue polarization from synergy of intracellular and extracellular auxin signaling |
title_short | Emergence of tissue polarization from synergy of intracellular and extracellular auxin signaling |
title_sort | emergence of tissue polarization from synergy of intracellular and extracellular auxin signaling |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3018162/ https://www.ncbi.nlm.nih.gov/pubmed/21179019 http://dx.doi.org/10.1038/msb.2010.103 |
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