AUTHOR=Li Chenglei , Yang Jingjing , Yang Kai , Wu Huala , Chen Hui , Wu Qi , Zhao Haixia 

TITLE=Tartary buckwheat FtF3′H1 as a metabolic branch switch to increase anthocyanin content in transgenic plant

JOURNAL=Frontiers in Plant Science

VOLUME=13

YEAR=2022

URL=https://www.frontiersin.org/journals/plant-science/articles/10.3389/fpls.2022.959698

DOI=10.3389/fpls.2022.959698

ISSN=1664-462X

ABSTRACT=<p>Tartary buckwheat (TB) is a pseudocereal rich in flavonoids, mainly including flavonols and anthocyanins. The flavonoid 3′-hydroxylase (F3′H) is a key enzyme in flavonoid biosynthesis and is encoded by two copies in TB genome. However, its biological function and effects on flavonol and anthocyanin synthesis in TB have not been well validated yet. In this study, we cloned the full-length <italic>FtF3′H1</italic> gene highly expressed in all tissues (compared with <italic>FtF3′H2</italic>) according to TB flowering transcriptome data. The corresponding FtF3′H1 protein contains 534 amino acids with the molecular properties of the typical plant F3′H and belongs to the CYP75B family. During the flowering stage, the <italic>FtF3′H1</italic> expression was highest in flowers, and its expression pattern showed a significant and positive correlation with the total flavonoids (<italic>R</italic><sup>2</sup> &gt; 0.95). The overexpression of <italic>FtF3′H1</italic> in <italic>Arabidopsis thaliana</italic>, <italic>Nicotiana tabacum</italic> and TB hairy roots resulted in a significant increase in anthocyanin contents (<italic>p</italic> &lt; 0.05) but a decrease in rutin (<italic>p</italic> &lt; 0.05). The average anthocyanin contents were 2.94 mg/g (fresh weight, FW) in <italic>A. thaliana</italic> (about 135% increase), 1.18 mg/g (FW) in <italic>tobacco</italic> (about 17% increase), and 1.56 mg/g (FW) TB hairy roots (about 44% increase), and the rutin contents were dropped to about 53.85, 14.99, 46.31%, respectively. However, the expression of genes involved in anthocyanin (DFRs and ANSs) and flavonol (FLSs) synthesis pathways were significantly upregulated (<italic>p</italic> &lt; 0.05). In particular, the expression level of <italic>DFR</italic>, a key enzyme that enters the anthocyanin branch, was upregulated thousand-fold in <italic>A. thaliana</italic> and in <italic>N. tabacum</italic>. These results might be attributed to <italic>FtF3′H1</italic> protein with a higher substrate preference for anthocyanin synthesis substrates. Altogether, we identified the basic biochemical activity of FtF3′H1 <italic>in vivo</italic> and investigated its involvement in anthocyanin and flavonol metabolism in plant.</p>