Cargando…

Model-based reconstruction of whole organ growth dynamics reveals invariant patterns in leaf morphogenesis

Plant organ morphogenesis spans several orders of magnitude in time and space. Because of limitations in live-imaging, analysing whole organ growth from initiation to mature stages typically rely on static data sampled from different timepoints and individuals. We introduce a new model-based strateg...

Descripción completa

Detalles Bibliográficos
Autores principales: Oughou, Mohamed, Biot, Eric, Arnaud, Nicolas, Maugarny-Calès, Aude, Laufs, Patrick, Andrey, Philippe, Burguet, Jasmine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cambridge University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10095959/
https://www.ncbi.nlm.nih.gov/pubmed/37077702
http://dx.doi.org/10.1017/qpb.2022.23
_version_ 1785024206516256768
author Oughou, Mohamed
Biot, Eric
Arnaud, Nicolas
Maugarny-Calès, Aude
Laufs, Patrick
Andrey, Philippe
Burguet, Jasmine
author_facet Oughou, Mohamed
Biot, Eric
Arnaud, Nicolas
Maugarny-Calès, Aude
Laufs, Patrick
Andrey, Philippe
Burguet, Jasmine
author_sort Oughou, Mohamed
collection PubMed
description Plant organ morphogenesis spans several orders of magnitude in time and space. Because of limitations in live-imaging, analysing whole organ growth from initiation to mature stages typically rely on static data sampled from different timepoints and individuals. We introduce a new model-based strategy for dating organs and for reconstructing morphogenetic trajectories over unlimited time windows based on static data. Using this approach, we show that Arabidopsis thaliana leaves are initiated at regular 1-day intervals. Despite contrasted adult morphologies, leaves of different ranks exhibited shared growth dynamics, with linear gradations of growth parameters according to leaf rank. At the sub-organ scale, successive serrations from same or different leaves also followed shared growth dynamics, suggesting that global and local leaf growth patterns are decoupled. Analysing mutants leaves with altered morphology highlighted the decorrelation between adult shapes and morphogenetic trajectories, thus stressing the benefits of our approach in identifying determinants and critical timepoints during organ morphogenesis.
format Online
Article
Text
id pubmed-10095959
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Cambridge University Press
record_format MEDLINE/PubMed
spelling pubmed-100959592023-04-18 Model-based reconstruction of whole organ growth dynamics reveals invariant patterns in leaf morphogenesis Oughou, Mohamed Biot, Eric Arnaud, Nicolas Maugarny-Calès, Aude Laufs, Patrick Andrey, Philippe Burguet, Jasmine Quant Plant Biol Original Research Article Plant organ morphogenesis spans several orders of magnitude in time and space. Because of limitations in live-imaging, analysing whole organ growth from initiation to mature stages typically rely on static data sampled from different timepoints and individuals. We introduce a new model-based strategy for dating organs and for reconstructing morphogenetic trajectories over unlimited time windows based on static data. Using this approach, we show that Arabidopsis thaliana leaves are initiated at regular 1-day intervals. Despite contrasted adult morphologies, leaves of different ranks exhibited shared growth dynamics, with linear gradations of growth parameters according to leaf rank. At the sub-organ scale, successive serrations from same or different leaves also followed shared growth dynamics, suggesting that global and local leaf growth patterns are decoupled. Analysing mutants leaves with altered morphology highlighted the decorrelation between adult shapes and morphogenetic trajectories, thus stressing the benefits of our approach in identifying determinants and critical timepoints during organ morphogenesis. Cambridge University Press 2023-02-03 /pmc/articles/PMC10095959/ /pubmed/37077702 http://dx.doi.org/10.1017/qpb.2022.23 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research Article
Oughou, Mohamed
Biot, Eric
Arnaud, Nicolas
Maugarny-Calès, Aude
Laufs, Patrick
Andrey, Philippe
Burguet, Jasmine
Model-based reconstruction of whole organ growth dynamics reveals invariant patterns in leaf morphogenesis
title Model-based reconstruction of whole organ growth dynamics reveals invariant patterns in leaf morphogenesis
title_full Model-based reconstruction of whole organ growth dynamics reveals invariant patterns in leaf morphogenesis
title_fullStr Model-based reconstruction of whole organ growth dynamics reveals invariant patterns in leaf morphogenesis
title_full_unstemmed Model-based reconstruction of whole organ growth dynamics reveals invariant patterns in leaf morphogenesis
title_short Model-based reconstruction of whole organ growth dynamics reveals invariant patterns in leaf morphogenesis
title_sort model-based reconstruction of whole organ growth dynamics reveals invariant patterns in leaf morphogenesis
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10095959/
https://www.ncbi.nlm.nih.gov/pubmed/37077702
http://dx.doi.org/10.1017/qpb.2022.23
work_keys_str_mv AT oughoumohamed modelbasedreconstructionofwholeorgangrowthdynamicsrevealsinvariantpatternsinleafmorphogenesis
AT bioteric modelbasedreconstructionofwholeorgangrowthdynamicsrevealsinvariantpatternsinleafmorphogenesis
AT arnaudnicolas modelbasedreconstructionofwholeorgangrowthdynamicsrevealsinvariantpatternsinleafmorphogenesis
AT maugarnycalesaude modelbasedreconstructionofwholeorgangrowthdynamicsrevealsinvariantpatternsinleafmorphogenesis
AT laufspatrick modelbasedreconstructionofwholeorgangrowthdynamicsrevealsinvariantpatternsinleafmorphogenesis
AT andreyphilippe modelbasedreconstructionofwholeorgangrowthdynamicsrevealsinvariantpatternsinleafmorphogenesis
AT burguetjasmine modelbasedreconstructionofwholeorgangrowthdynamicsrevealsinvariantpatternsinleafmorphogenesis