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A method to generate the surface cell layer of the 3D virtual shoot apex from apical initials

BACKGROUND: The development of cell pattern in the surface cell layer of the shoot apex can be investigated in vivo by use of a time-lapse confocal images, showing naked meristem in 3D in successive times. However, how this layer is originated from apical initials and develops as a result of growth...

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Autores principales: Kucypera, Krzysztof, Lipowczan, Marcin, Piekarska-Stachowiak, Anna, Nakielski, Jerzy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725887/
https://www.ncbi.nlm.nih.gov/pubmed/29238397
http://dx.doi.org/10.1186/s13007-017-0262-7
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author Kucypera, Krzysztof
Lipowczan, Marcin
Piekarska-Stachowiak, Anna
Nakielski, Jerzy
author_facet Kucypera, Krzysztof
Lipowczan, Marcin
Piekarska-Stachowiak, Anna
Nakielski, Jerzy
author_sort Kucypera, Krzysztof
collection PubMed
description BACKGROUND: The development of cell pattern in the surface cell layer of the shoot apex can be investigated in vivo by use of a time-lapse confocal images, showing naked meristem in 3D in successive times. However, how this layer is originated from apical initials and develops as a result of growth and divisions of their descendants, remains unknown. This is an open area for computer modelling. A method to generate the surface cell layer is presented on the example of the 3D paraboloidal shoot apical dome. In the used model the layer originates from three apical initials that meet at the dome summit and develops through growth and cell divisions under the isotropic surface growth, defined by the growth tensor. The cells, which are described by polyhedrons, divide anticlinally with the smallest division plane that passes depending on the used mode through the cell center, or the point found randomly near this center. The formation of the surface cell pattern is described with the attention being paid to activity of the apical initials and fates of their descendants. RESULTS: The computer generated surface layer that included about 350 cells required about 1200 divisions of the apical initials and their derivatives. The derivatives were arranged into three more or less equal clonal sectors composed of cellular clones at different age. Each apical initial renewed itself 7–8 times to produce the sector. In the shape and location and the cellular clones the following divisions of the initial were manifested. The application of the random factor resulted in more realistic cell pattern in comparison to the pure mode. The cell divisions were analyzed statistically on the top view. When all of the division walls were considered, their angular distribution was uniform, whereas in the distribution that was limited to apical initials only, some preferences related to their arrangement at the dome summit were observed. CONCLUSIONS: The realistic surface cell pattern was obtained. The present method is a useful tool to generate surface cell layer, study activity of initial cells and their derivatives, and how cell expansion and division are coordinated during growth. We expect its further application to clarify the question of a number and permanence or impermanence of initial cells, and possible relationship between their shape and oriented divisions, both on the ground of the growth tensor approach. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13007-017-0262-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-57258872017-12-13 A method to generate the surface cell layer of the 3D virtual shoot apex from apical initials Kucypera, Krzysztof Lipowczan, Marcin Piekarska-Stachowiak, Anna Nakielski, Jerzy Plant Methods Research BACKGROUND: The development of cell pattern in the surface cell layer of the shoot apex can be investigated in vivo by use of a time-lapse confocal images, showing naked meristem in 3D in successive times. However, how this layer is originated from apical initials and develops as a result of growth and divisions of their descendants, remains unknown. This is an open area for computer modelling. A method to generate the surface cell layer is presented on the example of the 3D paraboloidal shoot apical dome. In the used model the layer originates from three apical initials that meet at the dome summit and develops through growth and cell divisions under the isotropic surface growth, defined by the growth tensor. The cells, which are described by polyhedrons, divide anticlinally with the smallest division plane that passes depending on the used mode through the cell center, or the point found randomly near this center. The formation of the surface cell pattern is described with the attention being paid to activity of the apical initials and fates of their descendants. RESULTS: The computer generated surface layer that included about 350 cells required about 1200 divisions of the apical initials and their derivatives. The derivatives were arranged into three more or less equal clonal sectors composed of cellular clones at different age. Each apical initial renewed itself 7–8 times to produce the sector. In the shape and location and the cellular clones the following divisions of the initial were manifested. The application of the random factor resulted in more realistic cell pattern in comparison to the pure mode. The cell divisions were analyzed statistically on the top view. When all of the division walls were considered, their angular distribution was uniform, whereas in the distribution that was limited to apical initials only, some preferences related to their arrangement at the dome summit were observed. CONCLUSIONS: The realistic surface cell pattern was obtained. The present method is a useful tool to generate surface cell layer, study activity of initial cells and their derivatives, and how cell expansion and division are coordinated during growth. We expect its further application to clarify the question of a number and permanence or impermanence of initial cells, and possible relationship between their shape and oriented divisions, both on the ground of the growth tensor approach. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13007-017-0262-7) contains supplementary material, which is available to authorized users. BioMed Central 2017-12-11 /pmc/articles/PMC5725887/ /pubmed/29238397 http://dx.doi.org/10.1186/s13007-017-0262-7 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Kucypera, Krzysztof
Lipowczan, Marcin
Piekarska-Stachowiak, Anna
Nakielski, Jerzy
A method to generate the surface cell layer of the 3D virtual shoot apex from apical initials
title A method to generate the surface cell layer of the 3D virtual shoot apex from apical initials
title_full A method to generate the surface cell layer of the 3D virtual shoot apex from apical initials
title_fullStr A method to generate the surface cell layer of the 3D virtual shoot apex from apical initials
title_full_unstemmed A method to generate the surface cell layer of the 3D virtual shoot apex from apical initials
title_short A method to generate the surface cell layer of the 3D virtual shoot apex from apical initials
title_sort method to generate the surface cell layer of the 3d virtual shoot apex from apical initials
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725887/
https://www.ncbi.nlm.nih.gov/pubmed/29238397
http://dx.doi.org/10.1186/s13007-017-0262-7
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