A vacuolar hexose transport is required for xylem development in the inflorescence stem

Author:

Aubry Emilie12,Hoffmann Beate1ORCID,Vilaine Françoise1,Gilard Françoise3ORCID,Klemens Patrick A W4,Guérard Florence3,Gakière Bertrand3,Neuhaus H Ekkehard4ORCID,Bellini Catherine15ORCID,Dinant Sylvie1ORCID,Le Hir Rozenn1ORCID

Affiliation:

1. Institut Jean-Pierre Bourgin, INRAE, AgroParisTech, Université Paris-Saclay, 78000 Versailles, France

2. Ecole Doctorale 567 Sciences du Végétal, Univ Paris-Sud, Univ Paris-Saclay, bat 360, 91405 Orsay Cedex, France

3. Plateforme Métabolisme-Métabolome, Institute of Plant Sciences Paris-Saclay IPS2, CNRS, INRAE, Univ Paris Sud, Univ Evry, Univ Paris-Diderot, Sorbonne Paris-Cité, Université Paris-Saclay, Bâtiment 360, Rue de Noetzlin, 91192 Gif sur Yvette, France

4. Universität Kaiserslautern, Pflanzenphysiologie, Postfach 3049, D-67653 Kaiserslautern, Germany

5. Umeå Plant Science Centre, Department of Plant Physiology, Umeå University, 90187 Umeå, Sweden

Abstract

Abstract In Angiosperms, the development of the vascular system is controlled by a complex network of transcription factors. However, how nutrient availability in the vascular cells affects their development remains to be addressed. At the cellular level, cytosolic sugar availability is regulated mainly by sugar exchanges at the tonoplast through active and/or facilitated transport. In Arabidopsis (Arabidopsis thaliana), among the genes encoding tonoplastic transporters, SUGAR WILL EVENTUALLY BE EXPORTED TRANSPORTER 16 (SWEET16) and SWEET17 expression has been previously detected in the vascular system. Here, using a reverse genetics approach, we propose that sugar exchanges at the tonoplast, regulated by SWEET16, are important for xylem cell division as revealed in particular by the decreased number of xylem cells in the swt16 mutant and the accumulation of SWEET16 at the procambium–xylem boundary. In addition, we demonstrate that transport of hexoses mediated by SWEET16 and/or SWEET17 is required to sustain the formation of the xylem secondary cell wall. This result is in line with a defect in the xylem cell wall composition as measured by Fourier-transformed infrared spectroscopy in the swt16swt17 double mutant and by upregulation of several genes involved in secondary cell wall synthesis. Our work therefore supports a model in which xylem development partially depends on the exchange of hexoses at the tonoplast of xylem-forming cells.

Funder

support of IJPB’s Plant Observatory technological platforms and from a French State grant (Saclay Plant Sciences

French National Research Agency under an Investments for the Future program

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Genetics,Physiology

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