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Cell type boundaries organize plant development
In plants the dorsoventral boundary of leaves defines an axis of symmetry through the centre of the organ separating the top (dorsal) and bottom (ventral) tissues. Although the positioning of this boundary is critical for leaf morphogenesis, how the boundary is established and how it influences deve...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617630/ https://www.ncbi.nlm.nih.gov/pubmed/28895530 http://dx.doi.org/10.7554/eLife.27421 |
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author | Caggiano, Monica Pia Yu, Xiulian Bhatia, Neha Larsson, André Ram, Hasthi Ohno, Carolyn K Sappl, Pia Meyerowitz, Elliot M Jönsson, Henrik Heisler, Marcus G |
author_facet | Caggiano, Monica Pia Yu, Xiulian Bhatia, Neha Larsson, André Ram, Hasthi Ohno, Carolyn K Sappl, Pia Meyerowitz, Elliot M Jönsson, Henrik Heisler, Marcus G |
author_sort | Caggiano, Monica Pia |
collection | PubMed |
description | In plants the dorsoventral boundary of leaves defines an axis of symmetry through the centre of the organ separating the top (dorsal) and bottom (ventral) tissues. Although the positioning of this boundary is critical for leaf morphogenesis, how the boundary is established and how it influences development remains unclear. Using live-imaging and perturbation experiments we show that leaf orientation, morphology and position are pre-patterned by HD-ZIPIII and KAN gene expression in the shoot, leading to a model in which dorsoventral genes coordinate to regulate plant development by localizing auxin response between their expression domains. However we also find that auxin levels feedback on dorsoventral patterning by spatially organizing HD-ZIPIII and KAN expression in the shoot periphery. By demonstrating that the regulation of these genes by auxin also governs their response to wounds, our results also provide a parsimonious explanation for the influence of wounds on leaf dorsoventrality. |
format | Online Article Text |
id | pubmed-5617630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-56176302017-09-28 Cell type boundaries organize plant development Caggiano, Monica Pia Yu, Xiulian Bhatia, Neha Larsson, André Ram, Hasthi Ohno, Carolyn K Sappl, Pia Meyerowitz, Elliot M Jönsson, Henrik Heisler, Marcus G eLife Developmental Biology In plants the dorsoventral boundary of leaves defines an axis of symmetry through the centre of the organ separating the top (dorsal) and bottom (ventral) tissues. Although the positioning of this boundary is critical for leaf morphogenesis, how the boundary is established and how it influences development remains unclear. Using live-imaging and perturbation experiments we show that leaf orientation, morphology and position are pre-patterned by HD-ZIPIII and KAN gene expression in the shoot, leading to a model in which dorsoventral genes coordinate to regulate plant development by localizing auxin response between their expression domains. However we also find that auxin levels feedback on dorsoventral patterning by spatially organizing HD-ZIPIII and KAN expression in the shoot periphery. By demonstrating that the regulation of these genes by auxin also governs their response to wounds, our results also provide a parsimonious explanation for the influence of wounds on leaf dorsoventrality. eLife Sciences Publications, Ltd 2017-09-12 /pmc/articles/PMC5617630/ /pubmed/28895530 http://dx.doi.org/10.7554/eLife.27421 Text en © 2017, Caggiano et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Developmental Biology Caggiano, Monica Pia Yu, Xiulian Bhatia, Neha Larsson, André Ram, Hasthi Ohno, Carolyn K Sappl, Pia Meyerowitz, Elliot M Jönsson, Henrik Heisler, Marcus G Cell type boundaries organize plant development |
title | Cell type boundaries organize plant development |
title_full | Cell type boundaries organize plant development |
title_fullStr | Cell type boundaries organize plant development |
title_full_unstemmed | Cell type boundaries organize plant development |
title_short | Cell type boundaries organize plant development |
title_sort | cell type boundaries organize plant development |
topic | Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5617630/ https://www.ncbi.nlm.nih.gov/pubmed/28895530 http://dx.doi.org/10.7554/eLife.27421 |
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