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Bifacial cambium stem cells generate xylem and phloem during radial plant growth

A reduced rate of stem cell division is considered a widespread feature which ensures the integrity of genetic information during somatic development of plants and animals. Radial growth of plant shoots and roots is a stem cell-driven process that is fundamental for the mechanical and physiological...

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Autores principales: Shi, Dongbo, Lebovka, Ivan, López-Salmerón, Vadir, Sanchez, Pablo, Greb, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6340147/
https://www.ncbi.nlm.nih.gov/pubmed/30626594
http://dx.doi.org/10.1242/dev.171355
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author Shi, Dongbo
Lebovka, Ivan
López-Salmerón, Vadir
Sanchez, Pablo
Greb, Thomas
author_facet Shi, Dongbo
Lebovka, Ivan
López-Salmerón, Vadir
Sanchez, Pablo
Greb, Thomas
author_sort Shi, Dongbo
collection PubMed
description A reduced rate of stem cell division is considered a widespread feature which ensures the integrity of genetic information during somatic development of plants and animals. Radial growth of plant shoots and roots is a stem cell-driven process that is fundamental for the mechanical and physiological support of enlarging plant bodies. In most dicotyledonous species, the underlying stem cell niche, the cambium, generates xylem inwards and phloem outwards. Despite the importance and intriguing dynamics of the cambium, the functional characterization of its stem cells is hampered by the lack of experimental tools for accessing distinct cambium sub-domains. Here, we use the hypocotyl of Arabidopsis thaliana to map stem cell activity in the proliferating cambium. Through pulse labeling and genetically encoded lineage tracing, we find that a single bifacial stem cell generates both xylem and phloem cell lineages. This cell is characterized by a specific combination of PXY (TDR), SMXL5 and WOX4 gene activity and a high division rate in comparison with tissue-specific progenitors. Our analysis provides a cellular fate map of radial plant growth, and suggests that stem cell quiescence is not a general prerequisite for life-long tissue production. This article has an associated ‘The people behind the papers’ interview.
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spelling pubmed-63401472019-01-31 Bifacial cambium stem cells generate xylem and phloem during radial plant growth Shi, Dongbo Lebovka, Ivan López-Salmerón, Vadir Sanchez, Pablo Greb, Thomas Development Stem Cells and Regeneration A reduced rate of stem cell division is considered a widespread feature which ensures the integrity of genetic information during somatic development of plants and animals. Radial growth of plant shoots and roots is a stem cell-driven process that is fundamental for the mechanical and physiological support of enlarging plant bodies. In most dicotyledonous species, the underlying stem cell niche, the cambium, generates xylem inwards and phloem outwards. Despite the importance and intriguing dynamics of the cambium, the functional characterization of its stem cells is hampered by the lack of experimental tools for accessing distinct cambium sub-domains. Here, we use the hypocotyl of Arabidopsis thaliana to map stem cell activity in the proliferating cambium. Through pulse labeling and genetically encoded lineage tracing, we find that a single bifacial stem cell generates both xylem and phloem cell lineages. This cell is characterized by a specific combination of PXY (TDR), SMXL5 and WOX4 gene activity and a high division rate in comparison with tissue-specific progenitors. Our analysis provides a cellular fate map of radial plant growth, and suggests that stem cell quiescence is not a general prerequisite for life-long tissue production. This article has an associated ‘The people behind the papers’ interview. The Company of Biologists Ltd 2019-01-01 2019-01-09 /pmc/articles/PMC6340147/ /pubmed/30626594 http://dx.doi.org/10.1242/dev.171355 Text en © 2019. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/4.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Stem Cells and Regeneration
Shi, Dongbo
Lebovka, Ivan
López-Salmerón, Vadir
Sanchez, Pablo
Greb, Thomas
Bifacial cambium stem cells generate xylem and phloem during radial plant growth
title Bifacial cambium stem cells generate xylem and phloem during radial plant growth
title_full Bifacial cambium stem cells generate xylem and phloem during radial plant growth
title_fullStr Bifacial cambium stem cells generate xylem and phloem during radial plant growth
title_full_unstemmed Bifacial cambium stem cells generate xylem and phloem during radial plant growth
title_short Bifacial cambium stem cells generate xylem and phloem during radial plant growth
title_sort bifacial cambium stem cells generate xylem and phloem during radial plant growth
topic Stem Cells and Regeneration
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6340147/
https://www.ncbi.nlm.nih.gov/pubmed/30626594
http://dx.doi.org/10.1242/dev.171355
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