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Strictosidine activation in Apocynaceae: towards a "nuclear time bomb"?

BACKGROUND: The first two enzymatic steps of monoterpene indole alkaloid (MIA) biosynthetic pathway are catalysed by strictosidine synthase (STR) that condensates tryptamine and secologanin to form strictosidine and by strictosidine β-D-glucosidase (SGD) that subsequently hydrolyses the glucose moie...

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Autores principales: Guirimand, Grégory, Courdavault, Vincent, Lanoue, Arnaud, Mahroug, Samira, Guihur, Anthony, Blanc, Nathalie, Giglioli-Guivarc'h, Nathalie, St-Pierre, Benoit, Burlat, Vincent
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3095312/
https://www.ncbi.nlm.nih.gov/pubmed/20723215
http://dx.doi.org/10.1186/1471-2229-10-182
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author Guirimand, Grégory
Courdavault, Vincent
Lanoue, Arnaud
Mahroug, Samira
Guihur, Anthony
Blanc, Nathalie
Giglioli-Guivarc'h, Nathalie
St-Pierre, Benoit
Burlat, Vincent
author_facet Guirimand, Grégory
Courdavault, Vincent
Lanoue, Arnaud
Mahroug, Samira
Guihur, Anthony
Blanc, Nathalie
Giglioli-Guivarc'h, Nathalie
St-Pierre, Benoit
Burlat, Vincent
author_sort Guirimand, Grégory
collection PubMed
description BACKGROUND: The first two enzymatic steps of monoterpene indole alkaloid (MIA) biosynthetic pathway are catalysed by strictosidine synthase (STR) that condensates tryptamine and secologanin to form strictosidine and by strictosidine β-D-glucosidase (SGD) that subsequently hydrolyses the glucose moiety of strictosidine. The resulting unstable aglycon is rapidly converted into a highly reactive dialdehyde, from which more than 2,000 MIAs are derived. Many studies were conducted to elucidate the biosynthesis and regulation of pharmacologically valuable MIAs such as vinblastine and vincristine in Catharanthus roseus or ajmaline in Rauvolfia serpentina. However, very few reports focused on the MIA physiological functions. RESULTS: In this study we showed that a strictosidine pool existed in planta and that the strictosidine deglucosylation product(s) was (were) specifically responsible for in vitro protein cross-linking and precipitation suggesting a potential role for strictosidine activation in plant defence. The spatial feasibility of such an activation process was evaluated in planta. On the one hand, in situ hybridisation studies showed that CrSTR and CrSGD were coexpressed in the epidermal first barrier of C. roseus aerial organs. However, a combination of GFP-imaging, bimolecular fluorescence complementation and electromobility shift-zymogram experiments revealed that STR from both C. roseus and R. serpentina were localised to the vacuole whereas SGD from both species were shown to accumulate as highly stable supramolecular aggregates within the nucleus. Deletion and fusion studies allowed us to identify and to demonstrate the functionality of CrSTR and CrSGD targeting sequences. CONCLUSIONS: A spatial model was drawn to explain the role of the subcellular sequestration of STR and SGD to control the MIA metabolic flux under normal physiological conditions. The model also illustrates the possible mechanism of massive activation of the strictosidine vacuolar pool upon enzyme-substrate reunion occurring during potential herbivore feeding constituting a so-called "nuclear time bomb" in reference to the "mustard oil bomb" commonly used to describe the myrosinase-glucosinolate defence system in Brassicaceae.
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spelling pubmed-30953122011-05-17 Strictosidine activation in Apocynaceae: towards a "nuclear time bomb"? Guirimand, Grégory Courdavault, Vincent Lanoue, Arnaud Mahroug, Samira Guihur, Anthony Blanc, Nathalie Giglioli-Guivarc'h, Nathalie St-Pierre, Benoit Burlat, Vincent BMC Plant Biol Research Article BACKGROUND: The first two enzymatic steps of monoterpene indole alkaloid (MIA) biosynthetic pathway are catalysed by strictosidine synthase (STR) that condensates tryptamine and secologanin to form strictosidine and by strictosidine β-D-glucosidase (SGD) that subsequently hydrolyses the glucose moiety of strictosidine. The resulting unstable aglycon is rapidly converted into a highly reactive dialdehyde, from which more than 2,000 MIAs are derived. Many studies were conducted to elucidate the biosynthesis and regulation of pharmacologically valuable MIAs such as vinblastine and vincristine in Catharanthus roseus or ajmaline in Rauvolfia serpentina. However, very few reports focused on the MIA physiological functions. RESULTS: In this study we showed that a strictosidine pool existed in planta and that the strictosidine deglucosylation product(s) was (were) specifically responsible for in vitro protein cross-linking and precipitation suggesting a potential role for strictosidine activation in plant defence. The spatial feasibility of such an activation process was evaluated in planta. On the one hand, in situ hybridisation studies showed that CrSTR and CrSGD were coexpressed in the epidermal first barrier of C. roseus aerial organs. However, a combination of GFP-imaging, bimolecular fluorescence complementation and electromobility shift-zymogram experiments revealed that STR from both C. roseus and R. serpentina were localised to the vacuole whereas SGD from both species were shown to accumulate as highly stable supramolecular aggregates within the nucleus. Deletion and fusion studies allowed us to identify and to demonstrate the functionality of CrSTR and CrSGD targeting sequences. CONCLUSIONS: A spatial model was drawn to explain the role of the subcellular sequestration of STR and SGD to control the MIA metabolic flux under normal physiological conditions. The model also illustrates the possible mechanism of massive activation of the strictosidine vacuolar pool upon enzyme-substrate reunion occurring during potential herbivore feeding constituting a so-called "nuclear time bomb" in reference to the "mustard oil bomb" commonly used to describe the myrosinase-glucosinolate defence system in Brassicaceae. BioMed Central 2010-08-19 /pmc/articles/PMC3095312/ /pubmed/20723215 http://dx.doi.org/10.1186/1471-2229-10-182 Text en Copyright ©2010 Guirimand et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Guirimand, Grégory
Courdavault, Vincent
Lanoue, Arnaud
Mahroug, Samira
Guihur, Anthony
Blanc, Nathalie
Giglioli-Guivarc'h, Nathalie
St-Pierre, Benoit
Burlat, Vincent
Strictosidine activation in Apocynaceae: towards a "nuclear time bomb"?
title Strictosidine activation in Apocynaceae: towards a "nuclear time bomb"?
title_full Strictosidine activation in Apocynaceae: towards a "nuclear time bomb"?
title_fullStr Strictosidine activation in Apocynaceae: towards a "nuclear time bomb"?
title_full_unstemmed Strictosidine activation in Apocynaceae: towards a "nuclear time bomb"?
title_short Strictosidine activation in Apocynaceae: towards a "nuclear time bomb"?
title_sort strictosidine activation in apocynaceae: towards a "nuclear time bomb"?
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3095312/
https://www.ncbi.nlm.nih.gov/pubmed/20723215
http://dx.doi.org/10.1186/1471-2229-10-182
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