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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Main Authors: Ana Cecilia Aliaga Fandino, Hyoujin Kim, Jesse David Rademaker, Ji-Young Lee
Format: Article
Language:English
Published: The Company of Biologists 2019-03-01
Series:Biology Open
Subjects:
Online Access:http://bio.biologists.org/content/8/3/bio039677
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spelling doaj-f1b08d57e1e24db2a80dbfa4704bf7782021-06-02T15:44:10ZengThe Company of BiologistsBiology Open2046-63902019-03-018310.1242/bio.039677039677Reprogramming of the cambium regulators during adventitious root development upon wounding of storage tap roots in radish (Raphanus sativus L.)Ana Cecilia Aliaga Fandino0Hyoujin Kim1Jesse David Rademaker2Ji-Young Lee3 School of Biological Sciences, College of Natural Science, Seoul National University, 1 Gwanak-ro, Gwanak-gu, Seoul 08826, Republic of Korea School of Biological Sciences, College of Natural Science, Seoul National University, 1 Gwanak-ro, Gwanak-gu, Seoul 08826, Republic of Korea School of Biological Sciences, College of Natural Science, Seoul National University, 1 Gwanak-ro, Gwanak-gu, Seoul 08826, Republic of Korea School of Biological Sciences, College of Natural Science, Seoul National University, 1 Gwanak-ro, Gwanak-gu, Seoul 08826, Republic of Korea 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.http://bio.biologists.org/content/8/3/bio039677RadishAdventitious rootCambiumAuxinWOX11PXY-WOX4
collection DOAJ
language English
format Article
sources DOAJ
author Ana Cecilia Aliaga Fandino
Hyoujin Kim
Jesse David Rademaker
Ji-Young Lee
spellingShingle Ana Cecilia Aliaga Fandino
Hyoujin Kim
Jesse David Rademaker
Ji-Young Lee
Reprogramming of the cambium regulators during adventitious root development upon wounding of storage tap roots in radish (Raphanus sativus L.)
Biology Open
Radish
Adventitious root
Cambium
Auxin
WOX11
PXY-WOX4
author_facet Ana Cecilia Aliaga Fandino
Hyoujin Kim
Jesse David Rademaker
Ji-Young Lee
author_sort Ana Cecilia Aliaga Fandino
title 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_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_sort reprogramming of the cambium regulators during adventitious root development upon wounding of storage tap roots in radish (raphanus sativus l.)
publisher The Company of Biologists
series Biology Open
issn 2046-6390
publishDate 2019-03-01
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.
topic Radish
Adventitious root
Cambium
Auxin
WOX11
PXY-WOX4
url http://bio.biologists.org/content/8/3/bio039677
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