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AGAMOUS mediates timing of guard cell formation during gynoecium development

In Arabidopsis thaliana, stomata are composed of two guard cells that control the aperture of a central pore to facilitate gas exchange between the plant and its environment, which is particularly important during photosynthesis. Although leaves are the primary photosynthetic organs of flowering pla...

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Autores principales: Brazel, Ailbhe J., Fattorini, Róisín, McCarthy, Jesse, Franzen, Rainer, Rümpler, Florian, Coupland, George, Ó’Maoiléidigh, Diarmuid S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10593234/
https://www.ncbi.nlm.nih.gov/pubmed/37819989
http://dx.doi.org/10.1371/journal.pgen.1011000
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author Brazel, Ailbhe J.
Fattorini, Róisín
McCarthy, Jesse
Franzen, Rainer
Rümpler, Florian
Coupland, George
Ó’Maoiléidigh, Diarmuid S.
author_facet Brazel, Ailbhe J.
Fattorini, Róisín
McCarthy, Jesse
Franzen, Rainer
Rümpler, Florian
Coupland, George
Ó’Maoiléidigh, Diarmuid S.
author_sort Brazel, Ailbhe J.
collection PubMed
description In Arabidopsis thaliana, stomata are composed of two guard cells that control the aperture of a central pore to facilitate gas exchange between the plant and its environment, which is particularly important during photosynthesis. Although leaves are the primary photosynthetic organs of flowering plants, floral organs are also photosynthetically active. In the Brassicaceae, evidence suggests that silique photosynthesis is important for optimal seed oil content. A group of transcription factors containing MADS DNA binding domains is necessary and sufficient to confer floral organ identity. Elegant models, such as the ABCE model of flower development and the floral quartet model, have been instrumental in describing the molecular mechanisms by which these floral organ identity proteins govern flower development. However, we lack a complete understanding of how the floral organ identity genes interact with the underlying leaf development program. Here, we show that the MADS domain transcription factor AGAMOUS (AG) represses stomatal development on the gynoecial valves, so that maturation of stomatal complexes coincides with fertilization. We present evidence that this regulation by AG is mediated by direct transcriptional repression of a master regulator of the stomatal lineage, MUTE, and show data that suggests this interaction is conserved among several members of the Brassicaceae. This work extends our understanding of the mechanisms underlying floral organ formation and provides a framework to decipher the mechanisms that control floral organ photosynthesis.
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spelling pubmed-105932342023-10-24 AGAMOUS mediates timing of guard cell formation during gynoecium development Brazel, Ailbhe J. Fattorini, Róisín McCarthy, Jesse Franzen, Rainer Rümpler, Florian Coupland, George Ó’Maoiléidigh, Diarmuid S. PLoS Genet Research Article In Arabidopsis thaliana, stomata are composed of two guard cells that control the aperture of a central pore to facilitate gas exchange between the plant and its environment, which is particularly important during photosynthesis. Although leaves are the primary photosynthetic organs of flowering plants, floral organs are also photosynthetically active. In the Brassicaceae, evidence suggests that silique photosynthesis is important for optimal seed oil content. A group of transcription factors containing MADS DNA binding domains is necessary and sufficient to confer floral organ identity. Elegant models, such as the ABCE model of flower development and the floral quartet model, have been instrumental in describing the molecular mechanisms by which these floral organ identity proteins govern flower development. However, we lack a complete understanding of how the floral organ identity genes interact with the underlying leaf development program. Here, we show that the MADS domain transcription factor AGAMOUS (AG) represses stomatal development on the gynoecial valves, so that maturation of stomatal complexes coincides with fertilization. We present evidence that this regulation by AG is mediated by direct transcriptional repression of a master regulator of the stomatal lineage, MUTE, and show data that suggests this interaction is conserved among several members of the Brassicaceae. This work extends our understanding of the mechanisms underlying floral organ formation and provides a framework to decipher the mechanisms that control floral organ photosynthesis. Public Library of Science 2023-10-11 /pmc/articles/PMC10593234/ /pubmed/37819989 http://dx.doi.org/10.1371/journal.pgen.1011000 Text en © 2023 Brazel 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
Brazel, Ailbhe J.
Fattorini, Róisín
McCarthy, Jesse
Franzen, Rainer
Rümpler, Florian
Coupland, George
Ó’Maoiléidigh, Diarmuid S.
AGAMOUS mediates timing of guard cell formation during gynoecium development
title AGAMOUS mediates timing of guard cell formation during gynoecium development
title_full AGAMOUS mediates timing of guard cell formation during gynoecium development
title_fullStr AGAMOUS mediates timing of guard cell formation during gynoecium development
title_full_unstemmed AGAMOUS mediates timing of guard cell formation during gynoecium development
title_short AGAMOUS mediates timing of guard cell formation during gynoecium development
title_sort agamous mediates timing of guard cell formation during gynoecium development
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10593234/
https://www.ncbi.nlm.nih.gov/pubmed/37819989
http://dx.doi.org/10.1371/journal.pgen.1011000
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