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Noise and Robustness in Phyllotaxis

A striking feature of vascular plants is the regular arrangement of lateral organs on the stem, known as phyllotaxis. The most common phyllotactic patterns can be described using spirals, numbers from the Fibonacci sequence and the golden angle. This rich mathematical structure, along with the exper...

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Autores principales: Mirabet, Vincent, Besnard, Fabrice, Vernoux, Teva, Boudaoud, Arezki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3280957/
https://www.ncbi.nlm.nih.gov/pubmed/22359496
http://dx.doi.org/10.1371/journal.pcbi.1002389
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author Mirabet, Vincent
Besnard, Fabrice
Vernoux, Teva
Boudaoud, Arezki
author_facet Mirabet, Vincent
Besnard, Fabrice
Vernoux, Teva
Boudaoud, Arezki
author_sort Mirabet, Vincent
collection PubMed
description A striking feature of vascular plants is the regular arrangement of lateral organs on the stem, known as phyllotaxis. The most common phyllotactic patterns can be described using spirals, numbers from the Fibonacci sequence and the golden angle. This rich mathematical structure, along with the experimental reproduction of phyllotactic spirals in physical systems, has led to a view of phyllotaxis focusing on regularity. However all organisms are affected by natural stochastic variability, raising questions about the effect of this variability on phyllotaxis and the achievement of such regular patterns. Here we address these questions theoretically using a dynamical system of interacting sources of inhibitory field. Previous work has shown that phyllotaxis can emerge deterministically from the self-organization of such sources and that inhibition is primarily mediated by the depletion of the plant hormone auxin through polarized transport. We incorporated stochasticity in the model and found three main classes of defects in spiral phyllotaxis – the reversal of the handedness of spirals, the concomitant initiation of organs and the occurrence of distichous angles – and we investigated whether a secondary inhibitory field filters out defects. Our results are consistent with available experimental data and yield a prediction of the main source of stochasticity during organogenesis. Our model can be related to cellular parameters and thus provides a framework for the analysis of phyllotactic mutants at both cellular and tissular levels. We propose that secondary fields associated with organogenesis, such as other biochemical signals or mechanical forces, are important for the robustness of phyllotaxis. More generally, our work sheds light on how a target pattern can be achieved within a noisy background.
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spelling pubmed-32809572012-02-22 Noise and Robustness in Phyllotaxis Mirabet, Vincent Besnard, Fabrice Vernoux, Teva Boudaoud, Arezki PLoS Comput Biol Research Article A striking feature of vascular plants is the regular arrangement of lateral organs on the stem, known as phyllotaxis. The most common phyllotactic patterns can be described using spirals, numbers from the Fibonacci sequence and the golden angle. This rich mathematical structure, along with the experimental reproduction of phyllotactic spirals in physical systems, has led to a view of phyllotaxis focusing on regularity. However all organisms are affected by natural stochastic variability, raising questions about the effect of this variability on phyllotaxis and the achievement of such regular patterns. Here we address these questions theoretically using a dynamical system of interacting sources of inhibitory field. Previous work has shown that phyllotaxis can emerge deterministically from the self-organization of such sources and that inhibition is primarily mediated by the depletion of the plant hormone auxin through polarized transport. We incorporated stochasticity in the model and found three main classes of defects in spiral phyllotaxis – the reversal of the handedness of spirals, the concomitant initiation of organs and the occurrence of distichous angles – and we investigated whether a secondary inhibitory field filters out defects. Our results are consistent with available experimental data and yield a prediction of the main source of stochasticity during organogenesis. Our model can be related to cellular parameters and thus provides a framework for the analysis of phyllotactic mutants at both cellular and tissular levels. We propose that secondary fields associated with organogenesis, such as other biochemical signals or mechanical forces, are important for the robustness of phyllotaxis. More generally, our work sheds light on how a target pattern can be achieved within a noisy background. Public Library of Science 2012-02-16 /pmc/articles/PMC3280957/ /pubmed/22359496 http://dx.doi.org/10.1371/journal.pcbi.1002389 Text en Mirabet et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Mirabet, Vincent
Besnard, Fabrice
Vernoux, Teva
Boudaoud, Arezki
Noise and Robustness in Phyllotaxis
title Noise and Robustness in Phyllotaxis
title_full Noise and Robustness in Phyllotaxis
title_fullStr Noise and Robustness in Phyllotaxis
title_full_unstemmed Noise and Robustness in Phyllotaxis
title_short Noise and Robustness in Phyllotaxis
title_sort noise and robustness in phyllotaxis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3280957/
https://www.ncbi.nlm.nih.gov/pubmed/22359496
http://dx.doi.org/10.1371/journal.pcbi.1002389
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