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Epidermal injury-induced derepression of key regulator ATML1 in newly exposed cells elicits epidermis regeneration

Plant cell fate determination depends on the relative positions of the cells in developing organisms. The shoot epidermis, the outermost cell layer of the above-ground organs in land plants, protects plants from environmental stresses. How the shoot epidermis is formed only from the outermost cells...

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Autores principales: Iida, Hiroyuki, Mähönen, Ari Pekka, Jürgens, Gerd, Takada, Shinobu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9950045/
https://www.ncbi.nlm.nih.gov/pubmed/36823419
http://dx.doi.org/10.1038/s41467-023-36731-6
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author Iida, Hiroyuki
Mähönen, Ari Pekka
Jürgens, Gerd
Takada, Shinobu
author_facet Iida, Hiroyuki
Mähönen, Ari Pekka
Jürgens, Gerd
Takada, Shinobu
author_sort Iida, Hiroyuki
collection PubMed
description Plant cell fate determination depends on the relative positions of the cells in developing organisms. The shoot epidermis, the outermost cell layer of the above-ground organs in land plants, protects plants from environmental stresses. How the shoot epidermis is formed only from the outermost cells has remained unknown. Here we show that when inner leaf mesophyll cells are exposed to the surface, these cells show up-regulation of ATML1, a master regulator for epidermal cell identity in Arabidopsis thaliana. Epidermal cell types such as stomatal guard cells regenerate from young inner-lineage tissues that have a potential to accumulate ATML1 protein after epidermal injury. Surgical analyses indicate that application of pressure to the exposed site was sufficient to inhibit ATML1 derepression in the outermost mesophyll cells, suggesting this process requires pressure release. Furthermore, pharmacological analyses suggest that ATML1 derepression in the outermost mesophyll cells require cortical microtubule formation, MAPK signaling and proteasome activity. Our results suggest that surface-positional cues involving mechanical signaling are used to restrict ATML1 activity to the outermost cells and facilitate epidermal differentiation.
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spelling pubmed-99500452023-02-25 Epidermal injury-induced derepression of key regulator ATML1 in newly exposed cells elicits epidermis regeneration Iida, Hiroyuki Mähönen, Ari Pekka Jürgens, Gerd Takada, Shinobu Nat Commun Article Plant cell fate determination depends on the relative positions of the cells in developing organisms. The shoot epidermis, the outermost cell layer of the above-ground organs in land plants, protects plants from environmental stresses. How the shoot epidermis is formed only from the outermost cells has remained unknown. Here we show that when inner leaf mesophyll cells are exposed to the surface, these cells show up-regulation of ATML1, a master regulator for epidermal cell identity in Arabidopsis thaliana. Epidermal cell types such as stomatal guard cells regenerate from young inner-lineage tissues that have a potential to accumulate ATML1 protein after epidermal injury. Surgical analyses indicate that application of pressure to the exposed site was sufficient to inhibit ATML1 derepression in the outermost mesophyll cells, suggesting this process requires pressure release. Furthermore, pharmacological analyses suggest that ATML1 derepression in the outermost mesophyll cells require cortical microtubule formation, MAPK signaling and proteasome activity. Our results suggest that surface-positional cues involving mechanical signaling are used to restrict ATML1 activity to the outermost cells and facilitate epidermal differentiation. Nature Publishing Group UK 2023-02-23 /pmc/articles/PMC9950045/ /pubmed/36823419 http://dx.doi.org/10.1038/s41467-023-36731-6 Text en © The Author(s) 2023 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
Iida, Hiroyuki
Mähönen, Ari Pekka
Jürgens, Gerd
Takada, Shinobu
Epidermal injury-induced derepression of key regulator ATML1 in newly exposed cells elicits epidermis regeneration
title Epidermal injury-induced derepression of key regulator ATML1 in newly exposed cells elicits epidermis regeneration
title_full Epidermal injury-induced derepression of key regulator ATML1 in newly exposed cells elicits epidermis regeneration
title_fullStr Epidermal injury-induced derepression of key regulator ATML1 in newly exposed cells elicits epidermis regeneration
title_full_unstemmed Epidermal injury-induced derepression of key regulator ATML1 in newly exposed cells elicits epidermis regeneration
title_short Epidermal injury-induced derepression of key regulator ATML1 in newly exposed cells elicits epidermis regeneration
title_sort epidermal injury-induced derepression of key regulator atml1 in newly exposed cells elicits epidermis regeneration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9950045/
https://www.ncbi.nlm.nih.gov/pubmed/36823419
http://dx.doi.org/10.1038/s41467-023-36731-6
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AT jurgensgerd epidermalinjuryinducedderepressionofkeyregulatoratml1innewlyexposedcellselicitsepidermisregeneration
AT takadashinobu epidermalinjuryinducedderepressionofkeyregulatoratml1innewlyexposedcellselicitsepidermisregeneration