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The root meristem is shaped by brassinosteroid control of cell geometry

Growth extent and direction determine cell and whole-organ architecture. How they are spatio-temporally modulated to control size and shape is not well known. Here we tackled this question by studying the effect of brassinosteroid (BR) signalling on the structure of the root meristem. Quantification...

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Autores principales: Fridman, Y., Strauss, S., Horev, G., Ackerman-Lavert, M., Reiner-Benaim, A., Lane, B., Smith, R. S., Savaldi-Goldstein, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8592843/
https://www.ncbi.nlm.nih.gov/pubmed/34782771
http://dx.doi.org/10.1038/s41477-021-01014-9
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author Fridman, Y.
Strauss, S.
Horev, G.
Ackerman-Lavert, M.
Reiner-Benaim, A.
Lane, B.
Smith, R. S.
Savaldi-Goldstein, S.
author_facet Fridman, Y.
Strauss, S.
Horev, G.
Ackerman-Lavert, M.
Reiner-Benaim, A.
Lane, B.
Smith, R. S.
Savaldi-Goldstein, S.
author_sort Fridman, Y.
collection PubMed
description Growth extent and direction determine cell and whole-organ architecture. How they are spatio-temporally modulated to control size and shape is not well known. Here we tackled this question by studying the effect of brassinosteroid (BR) signalling on the structure of the root meristem. Quantification of the three-dimensional geometry of thousands of individual meristematic cells across different tissue types showed that the modulation of BR signalling yields distinct changes in growth rate and anisotropy, which affects the time that cells spend in the meristem and has a strong impact on the final root form. By contrast, the hormone effect on cell volume was minor, establishing cell volume as invariant to the effect of BR. Thus, BR has the highest effect on cell shape and growth anisotropy, regulating the overall longitudinal and radial growth of the meristem, while maintaining a coherent distribution of cell sizes. Moving from single-cell quantification to the whole organ, we developed a computational model of radial growth. The simulation demonstrates how differential BR-regulated growth between the inner and outer tissues shapes the meristem and thus explains the non-intuitive outcomes of tissue-specific perturbation of BR signalling. The combined experimental data and simulation suggest that the inner and outer tissues have distinct but coordinated roles in growth regulation.
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spelling pubmed-85928432021-11-23 The root meristem is shaped by brassinosteroid control of cell geometry Fridman, Y. Strauss, S. Horev, G. Ackerman-Lavert, M. Reiner-Benaim, A. Lane, B. Smith, R. S. Savaldi-Goldstein, S. Nat Plants Article Growth extent and direction determine cell and whole-organ architecture. How they are spatio-temporally modulated to control size and shape is not well known. Here we tackled this question by studying the effect of brassinosteroid (BR) signalling on the structure of the root meristem. Quantification of the three-dimensional geometry of thousands of individual meristematic cells across different tissue types showed that the modulation of BR signalling yields distinct changes in growth rate and anisotropy, which affects the time that cells spend in the meristem and has a strong impact on the final root form. By contrast, the hormone effect on cell volume was minor, establishing cell volume as invariant to the effect of BR. Thus, BR has the highest effect on cell shape and growth anisotropy, regulating the overall longitudinal and radial growth of the meristem, while maintaining a coherent distribution of cell sizes. Moving from single-cell quantification to the whole organ, we developed a computational model of radial growth. The simulation demonstrates how differential BR-regulated growth between the inner and outer tissues shapes the meristem and thus explains the non-intuitive outcomes of tissue-specific perturbation of BR signalling. The combined experimental data and simulation suggest that the inner and outer tissues have distinct but coordinated roles in growth regulation. Nature Publishing Group UK 2021-11-15 2021 /pmc/articles/PMC8592843/ /pubmed/34782771 http://dx.doi.org/10.1038/s41477-021-01014-9 Text en © The Author(s) 2021, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Fridman, Y.
Strauss, S.
Horev, G.
Ackerman-Lavert, M.
Reiner-Benaim, A.
Lane, B.
Smith, R. S.
Savaldi-Goldstein, S.
The root meristem is shaped by brassinosteroid control of cell geometry
title The root meristem is shaped by brassinosteroid control of cell geometry
title_full The root meristem is shaped by brassinosteroid control of cell geometry
title_fullStr The root meristem is shaped by brassinosteroid control of cell geometry
title_full_unstemmed The root meristem is shaped by brassinosteroid control of cell geometry
title_short The root meristem is shaped by brassinosteroid control of cell geometry
title_sort root meristem is shaped by brassinosteroid control of cell geometry
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8592843/
https://www.ncbi.nlm.nih.gov/pubmed/34782771
http://dx.doi.org/10.1038/s41477-021-01014-9
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