Journal
PLANT PHYSIOLOGY AND BIOCHEMISTRY
Volume 193, Issue -, Pages 124-138Publisher
ELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIER
DOI: 10.1016/j.plaphy.2022.10.023
Keywords
Ascorbate biosynthesis; Antioxidant activity; GDP-L-galactose phosphorylase; L-galactose-1-phosphate phosphatase; Gene expression; Ripening; Phytonutrients
Categories
Funding
- European Union [11SYN_3_480]
- GGET/EPANII, SYNERGASIA II NutriTom [T1EDK-01332/n-TOMATOMICS]
- Operational Program Competitiveness, Entrepreneurship, and Innovation
- [EU-FOOD-CT-2006-016214]
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This study aimed to enhance the AsA content in tomato fruit by overexpressing GDP-L-Galactose phosphorylase (GGP) and L-galactose-1-phosphate phosphatase (GPP). The transgenic lines showed increased levels of AsA without affecting fruit characteristics. RNA-Seq analysis revealed that the overexpression of GGP affected the expression of genes involved in cell wall modification, ethylene biosynthesis and signaling, pollen fertility, and carotenoid metabolism. This research provides valuable insights into the role of AsA induced genes in important traits, breeding programs, and gene editing approaches.
L-Ascorbic acid (AsA), a strong antioxidant, serves as an enzyme cofactor and redox status marker, modulating a plethora of biological processes. As tomato commercial varieties and hybrids possess relatively low amounts of AsA, the improvement of fruit AsA represents a strategic goal for enhanced human health. Previously, we have suggested that GDP-L-Galactose phosphorylase (GGP) and L-galactose-1-phosphate phosphatase (GPP) can serve as possible targets for AsA manipulation in tomato (Solanum lycopersicon L.) fruit. To this end, we produced and evaluated T3 transgenic tomato plants carrying these two genes under the control of CaMV-35S and two fruit specific promoters, PPC2 and PG-GGPI. The transgenic lines had elevated levels of AsA, with the PG-GGP1 line containing 3-fold more AsA than WT, without affecting fruit characteristics. Following RNA-Seq analysis, 164 and 13 DEGs were up- or down-regulated, respectively, between PG-GGP1 and WT pink fruits. PG-GGP1 fruit had a distinct number of up-regulated transcripts associated with cell wall modification, ethylene biosynthesis and signaling, pollen fertility and carotenoid metabolism. The elevated AsA accumulation resulted in the up regulation of AsA associated transcripts and alternative biosynthetic pathways suggesting that the entire metabolic pathway was influenced, probably via master regulation. We show here that AsA-fortification of tomato ripe fruit via GGP1 overexpression under the action of a fruit specific promoter PG affects fruit development and ripening, reduces ethylene production, and increased the levels of sugars, and carotenoids, supporting a robust database to further explore the role of AsA induced genes for agronomically important traits, breeding programs and precision gene editing approaches.
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