Exploring the metabolic and physiological roles of HQT in S. lycopersicum by gene editing

Front Plant Sci. 2023 Mar 31:14:1124959. doi: 10.3389/fpls.2023.1124959. eCollection 2023.

Abstract

The most abundant phenolic compound in Solanaceous plants is chlorogenic acid (CGA), which possesses protective properties such as antimicrobial and antioxidant activities. These properties are particularly relevant when plants are under adverse conditions, such as pathogen attack, excess light, or extreme temperatures that cause oxidative stress. Additionally, CGA has been shown to absorb UV-B light. In tomato and potato, CGA is mainly produced through the HQT pathway mediated by the enzyme hydroxycinnamoyl-CoA:quinate hydroxycinnamoyl transferase. However, the absence of natural or induced mutants of this gene has made it unclear whether other pathways contribute to CGA production and accumulation. To address this question, we used CRISPR technology to generate multiple knock-out mutant lines in the tomato HQT gene. The resulting slhqt plants did not accumulate CGA or other caffeoylquinic acids (CQAs) in various parts of the plant, indicating that CQA biosynthesis depends almost entirely on the HQT pathway in tomato and, likely, other Solanaceous crops. We also found that the lack of CGA in slhqt plants led to higher levels of hydroxycinnamoyl-glucose and flavonoids compared to wild-type plants. Gene expression analysis revealed that this metabolic reorganization was partly due to flux redirection, but also involved modulation of important transcription factor genes that regulate secondary metabolism and sense environmental conditions. Finally, we investigated the physiological role of CGA in tomato and found that it accumulates in the upper epidermis where it acts as a protector against UV-B irradiation.

Keywords: HQT; S. lycopersicum; UV-light stress; abiotic stresses; caffeoylquinic acids; genome editing; metabolic engineering; phenylpropanoid pathway.

Grants and funding

This study was carried out within the Agritech National Research Center and received funding from the European Union Next-GenerationEU (PIANO NAZIONALE DI RIPRESA E RESILIENZA (PNRR) – MISSIONE 4 COMPONENTE 2, INVESTIMENTO 1.4 – D.D. 1032 17/06/2022, CN00000022). This manuscript reflects only the authors’ views and opinions, neither the European Union nor the European Commission can be considered responsible for them. The research was also supported by BIOTECH-Cisget project from the Italian Ministry of Agriculture (MiPAAF D.M. 15924) (FD’O, MP and GM) and SMART-BREED project (A0375E0166, POR FESR LAZIO 2014 – 2020) (FD’O), the European-funded COST ACTION FA1106, QualityFruit, which supported FD’O with an STSM award. CM, WH, IA, TL, and JL were supported by the Institute Strategic Program Understanding and Exploiting Plant and Microbial Secondary Metabolism (grant number BB/J004596/1) from the BBSRC to John Innes Centre, and CM and JL acknowledge support from the EU H2020 project (grant number 679796) TomGEM.