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The response of the root proteome to the synthetic strigolactone GR24 in Arabidopsis

Authors :
Geert Goeminne
Jonathan Vandenbussche
François-Didier Boyer
Lukas Braem
Ruben Vanholme
Kris Gevaert
Alan Walton
Justine Fromentin
Sofie Goormachtig
Elisabeth Stes
Cedrick Matthys
An Staes
Carolien De Cuyper
Wout Boerjan
Marnik Vuylsteke
Department of plant systems biology
Flanders Institute for Biotechnology
Department of plant Biotechnology and Bioinformatics
University of Gent
Department of Biochemistry
Universiteit Gent = Ghent University [Belgium] (UGENT)
Institut Jean-Pierre Bourgin (IJPB)
Institut National de la Recherche Agronomique (INRA)-AgroParisTech
Centre National de la Recherche Scientifique (CNRS)
Laboratoire des interactions plantes micro-organismes (LIPM)
Institut National de la Recherche Agronomique (INRA)-Centre National de la Recherche Scientifique (CNRS)
Ghent University [AUGE/014]
European Cooperation on Science and Technology (COST action) [FA1206]
VIB International PhD program fellowship
Ghent University [Belgium] (UGENT)
Institut des Sciences des Plantes de Paris-Saclay (IPS2 (UMR_9213 / UMR_1403))
Institut National de la Recherche Agronomique (INRA)-Université Paris-Sud - Paris 11 (UP11)-Université Paris Diderot - Paris 7 (UPD7)-Université d'Évry-Val-d'Essonne (UEVE)-Centre National de la Recherche Scientifique (CNRS)
Source :
Molecular and Cellular Proteomics, Molecular and Cellular Proteomics, American Society for Biochemistry and Molecular Biology, 2016, 15 (8), pp.2744-2755. ⟨10.1074/mcp.M115.050062⟩, MOLECULAR & CELLULAR PROTEOMICS
Publication Year :
2016
Publisher :
HAL CCSD, 2016.

Abstract

International audience; Strigolactones are plant metabolites that act as phytohormones and rhizosphere signals. Whereas most research on unraveling the action mechanisms of strigolactones is focused on plant shoots, we investigated proteome adaptation during strigolactone signaling in the roots of Arabidopsis thaliana. Through large-scale, time-resolved, and quantitative proteomics, the impact of the strigolactone analog rac-GR24 was elucidated on the root proteome of the wild type and the signaling mutant more axillary growth 2 (max2). Our study revealed a clear MAX2-dependent rac-GR24 response: an increase in abundance of enzymes involved in flavonol biosynthesis, which was reduced in the max2-1 mutant. Mass spectrometry-driven metabolite profiling and thin-layer chromatography experiments demonstrated that these changes in protein expression lead to the accumulation of specific flavonols. Moreover, quantitative RT-PCR revealed that the flavonol-related protein expression profile was caused by rac-GR24-induced changes in transcript levels of the corresponding genes. This induction of flavonol production was shown to be activated by the two pure enantiomers that together make up rac-GR24. Finally, our data provide much needed clues concerning the multiple roles played by MAX2 in the roots and a comprehensive view of the rac-GR24-induced response in the root proteome.

Details

Language :
English
ISSN :
15359476 and 15359484
Database :
OpenAIRE
Journal :
Molecular and Cellular Proteomics, Molecular and Cellular Proteomics, American Society for Biochemistry and Molecular Biology, 2016, 15 (8), pp.2744-2755. ⟨10.1074/mcp.M115.050062⟩, MOLECULAR & CELLULAR PROTEOMICS
Accession number :
edsair.doi.dedup.....e7881b0fb5e9a67c4305ed07129ab508