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Geometric cues forecast the switch from two‐ to three‐dimensional growth in Physcomitrella patens
During land colonization, plants acquired a range of body plan adaptations, of which the innovation of three‐dimensional (3D) tissues increased organismal complexity and reproductivity. In the moss, Physcomitrella patens, a 3D leafy gametophore originates from filamentous cells that grow in a two‐di...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7027797/ https://www.ncbi.nlm.nih.gov/pubmed/31639220 http://dx.doi.org/10.1111/nph.16276 |
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author | Tang, Han Duijts, Kilian Bezanilla, Magdalena Scheres, Ben Vermeer, Joop E. M. Willemsen, Viola |
author_facet | Tang, Han Duijts, Kilian Bezanilla, Magdalena Scheres, Ben Vermeer, Joop E. M. Willemsen, Viola |
author_sort | Tang, Han |
collection | PubMed |
description | During land colonization, plants acquired a range of body plan adaptations, of which the innovation of three‐dimensional (3D) tissues increased organismal complexity and reproductivity. In the moss, Physcomitrella patens, a 3D leafy gametophore originates from filamentous cells that grow in a two‐dimensional (2D) plane through a series of asymmetric cell divisions. Asymmetric cell divisions that coincide with different cell division planes and growth directions enable the developmental switch from 2D to 3D, but insights into the underlying mechanisms coordinating this switch are still incomplete. Using 2D and 3D imaging and image segmentation, we characterized two geometric cues, the width of the initial cell and the angle of the transition division plane, which sufficiently distinguished a gametophore initial cell from a branch initial cell. These identified cues were further confirmed in gametophore formation mutants. The identification of a fluorescent marker allowed us to successfully predict the gametophore initial cell with > 90% accuracy before morphological changes, supporting our hypothesis that, before the transition division, parental cells of the gametophore initials possess different properties from those of the branch initials. Our results suggest that the cell fate decision of the initial cell is determined in the parental cell, before the transition division. |
format | Online Article Text |
id | pubmed-7027797 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70277972020-02-24 Geometric cues forecast the switch from two‐ to three‐dimensional growth in Physcomitrella patens Tang, Han Duijts, Kilian Bezanilla, Magdalena Scheres, Ben Vermeer, Joop E. M. Willemsen, Viola New Phytol Research During land colonization, plants acquired a range of body plan adaptations, of which the innovation of three‐dimensional (3D) tissues increased organismal complexity and reproductivity. In the moss, Physcomitrella patens, a 3D leafy gametophore originates from filamentous cells that grow in a two‐dimensional (2D) plane through a series of asymmetric cell divisions. Asymmetric cell divisions that coincide with different cell division planes and growth directions enable the developmental switch from 2D to 3D, but insights into the underlying mechanisms coordinating this switch are still incomplete. Using 2D and 3D imaging and image segmentation, we characterized two geometric cues, the width of the initial cell and the angle of the transition division plane, which sufficiently distinguished a gametophore initial cell from a branch initial cell. These identified cues were further confirmed in gametophore formation mutants. The identification of a fluorescent marker allowed us to successfully predict the gametophore initial cell with > 90% accuracy before morphological changes, supporting our hypothesis that, before the transition division, parental cells of the gametophore initials possess different properties from those of the branch initials. Our results suggest that the cell fate decision of the initial cell is determined in the parental cell, before the transition division. John Wiley and Sons Inc. 2019-12-03 2020-03 /pmc/articles/PMC7027797/ /pubmed/31639220 http://dx.doi.org/10.1111/nph.16276 Text en © 2019 The Authors. New Phytologist © 2019 New Phytologist Trust This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Tang, Han Duijts, Kilian Bezanilla, Magdalena Scheres, Ben Vermeer, Joop E. M. Willemsen, Viola Geometric cues forecast the switch from two‐ to three‐dimensional growth in Physcomitrella patens |
title | Geometric cues forecast the switch from two‐ to three‐dimensional growth in Physcomitrella patens
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title_full | Geometric cues forecast the switch from two‐ to three‐dimensional growth in Physcomitrella patens
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title_fullStr | Geometric cues forecast the switch from two‐ to three‐dimensional growth in Physcomitrella patens
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title_full_unstemmed | Geometric cues forecast the switch from two‐ to three‐dimensional growth in Physcomitrella patens
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title_short | Geometric cues forecast the switch from two‐ to three‐dimensional growth in Physcomitrella patens
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title_sort | geometric cues forecast the switch from two‐ to three‐dimensional growth in physcomitrella patens |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7027797/ https://www.ncbi.nlm.nih.gov/pubmed/31639220 http://dx.doi.org/10.1111/nph.16276 |
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