Blue light promotes ascorbate synthesis by deactivating the PAS/LOV photoreceptor that inhibits GDP-L-galactose phosphorylase

Author:

Bournonville Céline1ORCID,Mori Kentaro1ORCID,Deslous Paul1ORCID,Decros Guillaume1ORCID,Blomeier Tim2ORCID,Mauxion Jean-Philippe1ORCID,Jorly Joana1ORCID,Gadin Stéphanie1ORCID,Cassan Cédric1ORCID,Maucourt Mickael1ORCID,Just Daniel1ORCID,Brès Cécile1ORCID,Rothan Christophe1ORCID,Ferrand Carine1ORCID,Fernandez-Lochu Lucie1ORCID,Bataille Laure1ORCID,Miura Kenji3ORCID,Beven Laure1ORCID,Zurbriggen Matias D2ORCID,Pétriacq Pierre1ORCID,Gibon Yves1ORCID,Baldet Pierre1ORCID

Affiliation:

1. UMR 1332 Biologie du Fruit et Pathologie, Univ. Bordeaux, INRAE, 33883 Villenave d'Ornon , France

2. Institute of Synthetic Biology—CEPLAS—Faculty of Mathematics and Natural Sciences, Heinrich-Heine-Universität Düsseldorf , Dusseldorf 40225 , Germany

3. Tsukuba Innovation Plant Research Center, University of Tsukuba , 1-1-1 Tennodai, 305-8577 Ibaraki, Tsukuba , Japan

Abstract

Abstract Ascorbate (vitamin C) is an essential antioxidant in fresh fruits and vegetables. To gain insight into the regulation of ascorbate metabolism in plants, we studied mutant tomato plants (Solanum lycopersicum) that produce ascorbate-enriched fruits. The causal mutation, identified by a mapping-by-sequencing strategy, corresponded to a knock-out recessive mutation in a class of photoreceptor named PAS/LOV protein (PLP), which acts as a negative regulator of ascorbate biosynthesis. This trait was confirmed by CRISPR/Cas9 gene editing and further found in all plant organs, including fruit that accumulated 2 to 3 times more ascorbate than in the WT. The functional characterization revealed that PLP interacted with the 2 isoforms of GDP-L-galactose phosphorylase (GGP), known as the controlling step of the L-galactose pathway of ascorbate synthesis. The interaction with GGP occurred in the cytoplasm and the nucleus, but was abolished when PLP was truncated. These results were confirmed by a synthetic approach using an animal cell system, which additionally demonstrated that blue light modulated the PLP-GGP interaction. Assays performed in vitro with heterologously expressed GGP and PLP showed that PLP is a noncompetitive inhibitor of GGP that is inactivated after blue light exposure. This discovery provides a greater understanding of the light-dependent regulation of ascorbate metabolism in plants.

Funder

Région Aquitaine

Syngenta Seeds SAS

Plant Biology and Breeding Division of INRAE

Département Sciences de l’Environnement at the University of Bordeaux

INRAE BAP RARE

LIA FreQUenCE INRAE-Tsukuba University

Deutsche Forschungsgemeinschaft

Germany’s Excellence Strategy

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Plant Science

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