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An ancestral stomatal patterning module revealed in the non-vascular land plant Physcomitrella patens

The patterning of stomata plays a vital role in plant development and has emerged as a paradigm for the role of peptide signals in the spatial control of cellular differentiation. Research in Arabidopsis has identified a series of epidermal patterning factors (EPFs), which interact with an array of...

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Autores principales: Caine, Robert S., Chater, Caspar C., Kamisugi, Yasuko, Cuming, Andrew C., Beerling, David J., Gray, Julie E., Fleming, Andrew J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5047656/
https://www.ncbi.nlm.nih.gov/pubmed/27407102
http://dx.doi.org/10.1242/dev.135038
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author Caine, Robert S.
Chater, Caspar C.
Kamisugi, Yasuko
Cuming, Andrew C.
Beerling, David J.
Gray, Julie E.
Fleming, Andrew J.
author_facet Caine, Robert S.
Chater, Caspar C.
Kamisugi, Yasuko
Cuming, Andrew C.
Beerling, David J.
Gray, Julie E.
Fleming, Andrew J.
author_sort Caine, Robert S.
collection PubMed
description The patterning of stomata plays a vital role in plant development and has emerged as a paradigm for the role of peptide signals in the spatial control of cellular differentiation. Research in Arabidopsis has identified a series of epidermal patterning factors (EPFs), which interact with an array of membrane-localised receptors and associated proteins (encoded by ERECTA and TMM genes) to control stomatal density and distribution. However, although it is well-established that stomata arose very early in the evolution of land plants, until now it has been unclear whether the established angiosperm stomatal patterning system represented by the EPF/TMM/ERECTA module reflects a conserved, universal mechanism in the plant kingdom. Here, we use molecular genetics to show that the moss Physcomitrella patens has conserved homologues of angiosperm EPF, TMM and at least one ERECTA gene that function together to permit the correct patterning of stomata and that, moreover, elements of the module retain function when transferred to Arabidopsis. Our data characterise the stomatal patterning system in an evolutionarily distinct branch of plants and support the hypothesis that the EPF/TMM/ERECTA module represents an ancient patterning system.
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spelling pubmed-50476562016-10-06 An ancestral stomatal patterning module revealed in the non-vascular land plant Physcomitrella patens Caine, Robert S. Chater, Caspar C. Kamisugi, Yasuko Cuming, Andrew C. Beerling, David J. Gray, Julie E. Fleming, Andrew J. Development Research Article The patterning of stomata plays a vital role in plant development and has emerged as a paradigm for the role of peptide signals in the spatial control of cellular differentiation. Research in Arabidopsis has identified a series of epidermal patterning factors (EPFs), which interact with an array of membrane-localised receptors and associated proteins (encoded by ERECTA and TMM genes) to control stomatal density and distribution. However, although it is well-established that stomata arose very early in the evolution of land plants, until now it has been unclear whether the established angiosperm stomatal patterning system represented by the EPF/TMM/ERECTA module reflects a conserved, universal mechanism in the plant kingdom. Here, we use molecular genetics to show that the moss Physcomitrella patens has conserved homologues of angiosperm EPF, TMM and at least one ERECTA gene that function together to permit the correct patterning of stomata and that, moreover, elements of the module retain function when transferred to Arabidopsis. Our data characterise the stomatal patterning system in an evolutionarily distinct branch of plants and support the hypothesis that the EPF/TMM/ERECTA module represents an ancient patterning system. The Company of Biologists Ltd 2016-09-15 /pmc/articles/PMC5047656/ /pubmed/27407102 http://dx.doi.org/10.1242/dev.135038 Text en © 2016. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Caine, Robert S.
Chater, Caspar C.
Kamisugi, Yasuko
Cuming, Andrew C.
Beerling, David J.
Gray, Julie E.
Fleming, Andrew J.
An ancestral stomatal patterning module revealed in the non-vascular land plant Physcomitrella patens
title An ancestral stomatal patterning module revealed in the non-vascular land plant Physcomitrella patens
title_full An ancestral stomatal patterning module revealed in the non-vascular land plant Physcomitrella patens
title_fullStr An ancestral stomatal patterning module revealed in the non-vascular land plant Physcomitrella patens
title_full_unstemmed An ancestral stomatal patterning module revealed in the non-vascular land plant Physcomitrella patens
title_short An ancestral stomatal patterning module revealed in the non-vascular land plant Physcomitrella patens
title_sort ancestral stomatal patterning module revealed in the non-vascular land plant physcomitrella patens
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5047656/
https://www.ncbi.nlm.nih.gov/pubmed/27407102
http://dx.doi.org/10.1242/dev.135038
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