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Rhizosecretion of stele-synthesized glucosinolates and their catabolites requires GTR-mediated import in Arabidopsis

Casparian strip-generated apoplastic barriers not only control the radial flow of both water and ions but may also constitute a hindrance for the rhizosecretion of stele-synthesized phytochemicals. Here, we establish root-synthesized glucosinolates (GLS) are in Arabidopsis as a model to study the tr...

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Autores principales: Xu, Deyang, Hanschen, Franziska S, Witzel, Katja, Nintemann, Sebastian J, Nour-Eldin, Hussam Hassan, Schreiner, Monika, Halkier, Barbara Ann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5853541/
https://www.ncbi.nlm.nih.gov/pubmed/27702989
http://dx.doi.org/10.1093/jxb/erw355
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author Xu, Deyang
Hanschen, Franziska S
Witzel, Katja
Nintemann, Sebastian J
Nour-Eldin, Hussam Hassan
Schreiner, Monika
Halkier, Barbara Ann
author_facet Xu, Deyang
Hanschen, Franziska S
Witzel, Katja
Nintemann, Sebastian J
Nour-Eldin, Hussam Hassan
Schreiner, Monika
Halkier, Barbara Ann
author_sort Xu, Deyang
collection PubMed
description Casparian strip-generated apoplastic barriers not only control the radial flow of both water and ions but may also constitute a hindrance for the rhizosecretion of stele-synthesized phytochemicals. Here, we establish root-synthesized glucosinolates (GLS) are in Arabidopsis as a model to study the transport routes of plant-derived metabolites from the site of synthesis to the rhizosphere. Analysing the expression of GLS synthetic genes in the root indicate that the stele is the major site for the synthesis of aliphatic GLS, whereas indole GLS can be synthesized in both the stele and the cortex. Sampling root exudates from the wild type and the double mutant of the GLS importers GTR1 and GTR2 show that GTR-mediated retention of stele-synthesized GLS is a prerequisite for the exudation of both intact GLS and their catabolites into the rhizosphere. The expression of the GTRs inside the stele, combined with the previous observation that GLS are exported from biosynthetic cells, suggest three possible routes of stele-synthesized aliphatic GLS after their synthesis: (i) GTR-dependent import to cells symplastically connected to the cortical cells and the rhizosphere; (ii) GTR-independent transport via the xylem to the shoot; and (iii) GTR-dependent import to GLS-degrading myrosin cells at the cortex. The study suggests a previously undiscovered role of the import process in the rhizosecretion of root-synthesized phytochemicals.
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spelling pubmed-58535412018-07-27 Rhizosecretion of stele-synthesized glucosinolates and their catabolites requires GTR-mediated import in Arabidopsis Xu, Deyang Hanschen, Franziska S Witzel, Katja Nintemann, Sebastian J Nour-Eldin, Hussam Hassan Schreiner, Monika Halkier, Barbara Ann J Exp Bot Research Papers Casparian strip-generated apoplastic barriers not only control the radial flow of both water and ions but may also constitute a hindrance for the rhizosecretion of stele-synthesized phytochemicals. Here, we establish root-synthesized glucosinolates (GLS) are in Arabidopsis as a model to study the transport routes of plant-derived metabolites from the site of synthesis to the rhizosphere. Analysing the expression of GLS synthetic genes in the root indicate that the stele is the major site for the synthesis of aliphatic GLS, whereas indole GLS can be synthesized in both the stele and the cortex. Sampling root exudates from the wild type and the double mutant of the GLS importers GTR1 and GTR2 show that GTR-mediated retention of stele-synthesized GLS is a prerequisite for the exudation of both intact GLS and their catabolites into the rhizosphere. The expression of the GTRs inside the stele, combined with the previous observation that GLS are exported from biosynthetic cells, suggest three possible routes of stele-synthesized aliphatic GLS after their synthesis: (i) GTR-dependent import to cells symplastically connected to the cortical cells and the rhizosphere; (ii) GTR-independent transport via the xylem to the shoot; and (iii) GTR-dependent import to GLS-degrading myrosin cells at the cortex. The study suggests a previously undiscovered role of the import process in the rhizosecretion of root-synthesized phytochemicals. Oxford University Press 2017-06-01 2016-10-04 /pmc/articles/PMC5853541/ /pubmed/27702989 http://dx.doi.org/10.1093/jxb/erw355 Text en © The Author 2016. Published by Oxford University Press on behalf of the Society for Experimental Biology. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Papers
Xu, Deyang
Hanschen, Franziska S
Witzel, Katja
Nintemann, Sebastian J
Nour-Eldin, Hussam Hassan
Schreiner, Monika
Halkier, Barbara Ann
Rhizosecretion of stele-synthesized glucosinolates and their catabolites requires GTR-mediated import in Arabidopsis
title Rhizosecretion of stele-synthesized glucosinolates and their catabolites requires GTR-mediated import in Arabidopsis
title_full Rhizosecretion of stele-synthesized glucosinolates and their catabolites requires GTR-mediated import in Arabidopsis
title_fullStr Rhizosecretion of stele-synthesized glucosinolates and their catabolites requires GTR-mediated import in Arabidopsis
title_full_unstemmed Rhizosecretion of stele-synthesized glucosinolates and their catabolites requires GTR-mediated import in Arabidopsis
title_short Rhizosecretion of stele-synthesized glucosinolates and their catabolites requires GTR-mediated import in Arabidopsis
title_sort rhizosecretion of stele-synthesized glucosinolates and their catabolites requires gtr-mediated import in arabidopsis
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5853541/
https://www.ncbi.nlm.nih.gov/pubmed/27702989
http://dx.doi.org/10.1093/jxb/erw355
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