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Combined computational modeling and experimental analysis integrating chemical and mechanical signals suggests possible mechanism of shoot meristem maintenance
Stem cell maintenance in multilayered shoot apical meristems (SAMs) of plants requires strict regulation of cell growth and division. Exactly how the complex milieu of chemical and mechanical signals interact in the central region of the SAM to regulate cell division plane orientation is not well un...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9249181/ https://www.ncbi.nlm.nih.gov/pubmed/35727850 http://dx.doi.org/10.1371/journal.pcbi.1010199 |
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author | Banwarth-Kuhn, Mikahl Rodriguez, Kevin Michael, Christian Ta, Calvin-Khang Plong, Alexander Bourgain-Chang, Eric Nematbakhsh, Ali Chen, Weitao Roy-Chowdhury, Amit Reddy, G. Venugopala Alber, Mark |
author_facet | Banwarth-Kuhn, Mikahl Rodriguez, Kevin Michael, Christian Ta, Calvin-Khang Plong, Alexander Bourgain-Chang, Eric Nematbakhsh, Ali Chen, Weitao Roy-Chowdhury, Amit Reddy, G. Venugopala Alber, Mark |
author_sort | Banwarth-Kuhn, Mikahl |
collection | PubMed |
description | Stem cell maintenance in multilayered shoot apical meristems (SAMs) of plants requires strict regulation of cell growth and division. Exactly how the complex milieu of chemical and mechanical signals interact in the central region of the SAM to regulate cell division plane orientation is not well understood. In this paper, simulations using a newly developed multiscale computational model are combined with experimental studies to suggest and test three hypothesized mechanisms for the regulation of cell division plane orientation and the direction of anisotropic cell expansion in the corpus. Simulations predict that in the Apical corpus, WUSCHEL and cytokinin regulate the direction of anisotropic cell expansion, and cells divide according to tensile stress on the cell wall. In the Basal corpus, model simulations suggest dual roles for WUSCHEL and cytokinin in regulating both the direction of anisotropic cell expansion and cell division plane orientation. Simulation results are followed by a detailed analysis of changes in cell characteristics upon manipulation of WUSCHEL and cytokinin in experiments that support model predictions. Moreover, simulations predict that this layer-specific mechanism maintains both the experimentally observed shape and structure of the SAM as well as the distribution of WUSCHEL in the tissue. This provides an additional link between the roles of WUSCHEL, cytokinin, and mechanical stress in regulating SAM growth and proper stem cell maintenance in the SAM. |
format | Online Article Text |
id | pubmed-9249181 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-92491812022-07-02 Combined computational modeling and experimental analysis integrating chemical and mechanical signals suggests possible mechanism of shoot meristem maintenance Banwarth-Kuhn, Mikahl Rodriguez, Kevin Michael, Christian Ta, Calvin-Khang Plong, Alexander Bourgain-Chang, Eric Nematbakhsh, Ali Chen, Weitao Roy-Chowdhury, Amit Reddy, G. Venugopala Alber, Mark PLoS Comput Biol Research Article Stem cell maintenance in multilayered shoot apical meristems (SAMs) of plants requires strict regulation of cell growth and division. Exactly how the complex milieu of chemical and mechanical signals interact in the central region of the SAM to regulate cell division plane orientation is not well understood. In this paper, simulations using a newly developed multiscale computational model are combined with experimental studies to suggest and test three hypothesized mechanisms for the regulation of cell division plane orientation and the direction of anisotropic cell expansion in the corpus. Simulations predict that in the Apical corpus, WUSCHEL and cytokinin regulate the direction of anisotropic cell expansion, and cells divide according to tensile stress on the cell wall. In the Basal corpus, model simulations suggest dual roles for WUSCHEL and cytokinin in regulating both the direction of anisotropic cell expansion and cell division plane orientation. Simulation results are followed by a detailed analysis of changes in cell characteristics upon manipulation of WUSCHEL and cytokinin in experiments that support model predictions. Moreover, simulations predict that this layer-specific mechanism maintains both the experimentally observed shape and structure of the SAM as well as the distribution of WUSCHEL in the tissue. This provides an additional link between the roles of WUSCHEL, cytokinin, and mechanical stress in regulating SAM growth and proper stem cell maintenance in the SAM. Public Library of Science 2022-06-21 /pmc/articles/PMC9249181/ /pubmed/35727850 http://dx.doi.org/10.1371/journal.pcbi.1010199 Text en © 2022 Banwarth-Kuhn et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Banwarth-Kuhn, Mikahl Rodriguez, Kevin Michael, Christian Ta, Calvin-Khang Plong, Alexander Bourgain-Chang, Eric Nematbakhsh, Ali Chen, Weitao Roy-Chowdhury, Amit Reddy, G. Venugopala Alber, Mark Combined computational modeling and experimental analysis integrating chemical and mechanical signals suggests possible mechanism of shoot meristem maintenance |
title | Combined computational modeling and experimental analysis integrating chemical and mechanical signals suggests possible mechanism of shoot meristem maintenance |
title_full | Combined computational modeling and experimental analysis integrating chemical and mechanical signals suggests possible mechanism of shoot meristem maintenance |
title_fullStr | Combined computational modeling and experimental analysis integrating chemical and mechanical signals suggests possible mechanism of shoot meristem maintenance |
title_full_unstemmed | Combined computational modeling and experimental analysis integrating chemical and mechanical signals suggests possible mechanism of shoot meristem maintenance |
title_short | Combined computational modeling and experimental analysis integrating chemical and mechanical signals suggests possible mechanism of shoot meristem maintenance |
title_sort | combined computational modeling and experimental analysis integrating chemical and mechanical signals suggests possible mechanism of shoot meristem maintenance |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9249181/ https://www.ncbi.nlm.nih.gov/pubmed/35727850 http://dx.doi.org/10.1371/journal.pcbi.1010199 |
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