Arabidopsis hydathodes are sites of auxin accumulation and nutrient scavenging

Author:

Routaboul Jean‐Marc1ORCID,Bellenot Caroline1,Olympio Aurore2,Clément Gilles3,Citerne Sylvie3,Remblière Céline1,Charvin Magali4,Franke Lars5,Chiarenza Serge2,Vasselon Damien3,Jardinaud Marie‐Françoise1,Carrère Sébastien1,Nussaume Laurent2ORCID,Laufs Patrick3ORCID,Leonhardt Nathalie2,Navarro Lionel4,Schattat Martin5,Noël Laurent D.1ORCID

Affiliation:

1. Laboratoire des Interactions Plantes‐Microbes‐Environnement (LIPME) Université de Toulouse, INRAE UMR 0441, CNRS UMR 2598 Castanet‐Tolosan F‐31326 France

2. Institut de Biosciences et Biotechnologies d'Aix‐Marseille Aix‐Marseille Université, CEA, CNRS UMR 7265 Saint Paul‐Lez‐Durance F‐13108 France

3. Institute Jean‐Pierre Bourgin for Plant Sciences (IJPB), Université Paris‐Saclay, INRAE, AgroParisTech Versailles 78000 France

4. Institut de Biologie de l'Ecole Normale Supérieure (IBENS) CNRS UMR8197, INSERM U1024 Paris 75005 France

5. Department of Plant Physiology, Institute for Biology Martin‐Luther‐University Halle‐Wittenberg Halle (Saale) D‐06120 Germany

Abstract

SUMMARYHydathodes are small organs found on the leaf margins of vascular plants which release excess xylem sap through a process called guttation. While previous studies have hinted at additional functions of hydathode in metabolite transport or auxin metabolism, experimental support is limited. We conducted comprehensive transcriptomic, metabolomic and physiological analyses of mature Arabidopsis hydathodes. This study identified 1460 genes differentially expressed in hydathodes compared to leaf blades, indicating higher expression of most genes associated with auxin metabolism, metabolite transport, stress response, DNA, RNA or microRNA processes, plant cell wall dynamics and wax metabolism. Notably, we observed differential expression of genes encoding auxin‐related transcriptional regulators, biosynthetic processes, transport and vacuolar storage supported by the measured accumulation of free and conjugated auxin in hydathodes. We also showed that 78% of the total content of 52 xylem metabolites was removed from guttation fluid at hydathodes. We demonstrate that NRT2.1 and PHT1;4 transporters capture nitrate and inorganic phosphate in guttation fluid, respectively, thus limiting the loss of nutrients during this process. Our transcriptomic and metabolomic analyses unveil an organ with its specific physiological and biological identity.

Funder

Agence Nationale de la Recherche

Publisher

Wiley

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