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Reprogramming of the cambium regulators during adventitious root development upon wounding of storage tap roots in radish (Raphanus sativus L.)

Cambium contains a stem cell population that produces xylem and phloem tissues in a radial direction during the secondary growth stage. The growth of many storage roots, including in the radish, Raphanus sativus L., also depends on cambium. Interestingly, we observed numerous adventitious roots (ARs...

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Autores principales: Aliaga Fandino, Ana Cecilia, Kim, Hyoujin, Rademaker, Jesse David, Lee, Ji-Young
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/PMC6451342/
https://www.ncbi.nlm.nih.gov/pubmed/30787007
http://dx.doi.org/10.1242/bio.039677
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author Aliaga Fandino, Ana Cecilia
Kim, Hyoujin
Rademaker, Jesse David
Lee, Ji-Young
author_facet Aliaga Fandino, Ana Cecilia
Kim, Hyoujin
Rademaker, Jesse David
Lee, Ji-Young
author_sort Aliaga Fandino, Ana Cecilia
collection PubMed
description Cambium contains a stem cell population that produces xylem and phloem tissues in a radial direction during the secondary growth stage. The growth of many storage roots, including in the radish, Raphanus sativus L., also depends on cambium. Interestingly, we observed numerous adventitious roots (ARs) emerging from the cambia of cut surfaces when the bases of radish storage tap roots were removed. Previous studies in Arabidopsis showed that the WOX11/12 pathway regulates AR initiation and meristem establishment in an auxin-dependent manner. Here, we provide evidence indicating the evolutionary conservation of the WOX11/12 pathway during the AR development in radishes. Additionally, we found that expression of two cambium regulators, PXY and WOX4, is induced in the cambium regions that are connected to emerging ARs via vascularization. Both AR formation and genes associated with this were induced by exogenous auxin. Our research suggests that some key cambium regulators might be reprogrammed to aid in the AR development in concert with the WOX11/12 pathway. This article has an associated First Person interview with the first author of the paper.
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spelling pubmed-64513422019-04-08 Reprogramming of the cambium regulators during adventitious root development upon wounding of storage tap roots in radish (Raphanus sativus L.) Aliaga Fandino, Ana Cecilia Kim, Hyoujin Rademaker, Jesse David Lee, Ji-Young Biol Open Research Article Cambium contains a stem cell population that produces xylem and phloem tissues in a radial direction during the secondary growth stage. The growth of many storage roots, including in the radish, Raphanus sativus L., also depends on cambium. Interestingly, we observed numerous adventitious roots (ARs) emerging from the cambia of cut surfaces when the bases of radish storage tap roots were removed. Previous studies in Arabidopsis showed that the WOX11/12 pathway regulates AR initiation and meristem establishment in an auxin-dependent manner. Here, we provide evidence indicating the evolutionary conservation of the WOX11/12 pathway during the AR development in radishes. Additionally, we found that expression of two cambium regulators, PXY and WOX4, is induced in the cambium regions that are connected to emerging ARs via vascularization. Both AR formation and genes associated with this were induced by exogenous auxin. Our research suggests that some key cambium regulators might be reprogrammed to aid in the AR development in concert with the WOX11/12 pathway. This article has an associated First Person interview with the first author of the paper. The Company of Biologists Ltd 2019-02-20 /pmc/articles/PMC6451342/ /pubmed/30787007 http://dx.doi.org/10.1242/bio.039677 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 Research Article
Aliaga Fandino, Ana Cecilia
Kim, Hyoujin
Rademaker, Jesse David
Lee, Ji-Young
Reprogramming of the cambium regulators during adventitious root development upon wounding of storage tap roots in radish (Raphanus sativus L.)
title Reprogramming of the cambium regulators during adventitious root development upon wounding of storage tap roots in radish (Raphanus sativus L.)
title_full Reprogramming of the cambium regulators during adventitious root development upon wounding of storage tap roots in radish (Raphanus sativus L.)
title_fullStr Reprogramming of the cambium regulators during adventitious root development upon wounding of storage tap roots in radish (Raphanus sativus L.)
title_full_unstemmed Reprogramming of the cambium regulators during adventitious root development upon wounding of storage tap roots in radish (Raphanus sativus L.)
title_short Reprogramming of the cambium regulators during adventitious root development upon wounding of storage tap roots in radish (Raphanus sativus L.)
title_sort reprogramming of the cambium regulators during adventitious root development upon wounding of storage tap roots in radish (raphanus sativus l.)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6451342/
https://www.ncbi.nlm.nih.gov/pubmed/30787007
http://dx.doi.org/10.1242/bio.039677
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