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A biomechanical model of anther opening reveals the roles of dehydration and secondary thickening

Understanding the processes that underlie pollen release is a prime target for controlling fertility to enable selective breeding and the efficient production of hybrid crops. Pollen release requires anther opening, which involves changes in the biomechanical properties of the anther wall. In this r...

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Detalles Bibliográficos
Autores principales: Nelson, M R, Band, L R, Dyson, R J, Lessinnes, T, Wells, D M, Yang, C, Everitt, N M, Jensen, O E, Wilson, Z A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569878/
https://www.ncbi.nlm.nih.gov/pubmed/22998410
http://dx.doi.org/10.1111/j.1469-8137.2012.04329.x
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author Nelson, M R
Band, L R
Dyson, R J
Lessinnes, T
Wells, D M
Yang, C
Everitt, N M
Jensen, O E
Wilson, Z A
author_facet Nelson, M R
Band, L R
Dyson, R J
Lessinnes, T
Wells, D M
Yang, C
Everitt, N M
Jensen, O E
Wilson, Z A
author_sort Nelson, M R
collection PubMed
description Understanding the processes that underlie pollen release is a prime target for controlling fertility to enable selective breeding and the efficient production of hybrid crops. Pollen release requires anther opening, which involves changes in the biomechanical properties of the anther wall. In this research, we develop and use a mathematical model to understand how these biomechanical processes lead to anther opening. Our mathematical model describing the biomechanics of anther opening incorporates the bilayer structure of the mature anther wall, which comprises the outer epidermal cell layer, whose turgor pressure is related to its hydration, and the endothecial layer, whose walls contain helical secondary thickening, which resists stretching and bending. The model describes how epidermal dehydration, in association with the thickened endothecial layer, creates forces within the anther wall causing it to bend outwards, resulting in anther opening and pollen release. The model demonstrates that epidermal dehydration can drive anther opening, and suggests why endothecial secondary thickening is essential for this process (explaining the phenotypes presented in the myb26 and nst1nst2 mutants). The research hypothesizes and demonstrates a biomechanical mechanism for anther opening, which appears to be conserved in many other biological situations where tissue movement occurs.
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spelling pubmed-35698782013-02-25 A biomechanical model of anther opening reveals the roles of dehydration and secondary thickening Nelson, M R Band, L R Dyson, R J Lessinnes, T Wells, D M Yang, C Everitt, N M Jensen, O E Wilson, Z A New Phytol Research Understanding the processes that underlie pollen release is a prime target for controlling fertility to enable selective breeding and the efficient production of hybrid crops. Pollen release requires anther opening, which involves changes in the biomechanical properties of the anther wall. In this research, we develop and use a mathematical model to understand how these biomechanical processes lead to anther opening. Our mathematical model describing the biomechanics of anther opening incorporates the bilayer structure of the mature anther wall, which comprises the outer epidermal cell layer, whose turgor pressure is related to its hydration, and the endothecial layer, whose walls contain helical secondary thickening, which resists stretching and bending. The model describes how epidermal dehydration, in association with the thickened endothecial layer, creates forces within the anther wall causing it to bend outwards, resulting in anther opening and pollen release. The model demonstrates that epidermal dehydration can drive anther opening, and suggests why endothecial secondary thickening is essential for this process (explaining the phenotypes presented in the myb26 and nst1nst2 mutants). The research hypothesizes and demonstrates a biomechanical mechanism for anther opening, which appears to be conserved in many other biological situations where tissue movement occurs. Blackwell Publishing Ltd 2012-12 2012-09-21 /pmc/articles/PMC3569878/ /pubmed/22998410 http://dx.doi.org/10.1111/j.1469-8137.2012.04329.x Text en Copyright © 2012 New Phytologist Trust http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation.
spellingShingle Research
Nelson, M R
Band, L R
Dyson, R J
Lessinnes, T
Wells, D M
Yang, C
Everitt, N M
Jensen, O E
Wilson, Z A
A biomechanical model of anther opening reveals the roles of dehydration and secondary thickening
title A biomechanical model of anther opening reveals the roles of dehydration and secondary thickening
title_full A biomechanical model of anther opening reveals the roles of dehydration and secondary thickening
title_fullStr A biomechanical model of anther opening reveals the roles of dehydration and secondary thickening
title_full_unstemmed A biomechanical model of anther opening reveals the roles of dehydration and secondary thickening
title_short A biomechanical model of anther opening reveals the roles of dehydration and secondary thickening
title_sort biomechanical model of anther opening reveals the roles of dehydration and secondary thickening
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569878/
https://www.ncbi.nlm.nih.gov/pubmed/22998410
http://dx.doi.org/10.1111/j.1469-8137.2012.04329.x
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