Wuhan Botanical Garden, Chinese Academy of Sciences, Jiufeng 1 Road, Wuhan, 430074, Hubei, China.
College of Life Sciences, University of Chinese Academy of Sciences, 19A Yuquan Road, Beijing, 100049, China.
New Phytol. 2022 Jun;234(5):1782-1800. doi: 10.1111/nph.18097. Epub 2022 Mar 31.
Plant-derived Vitamin C (l-ascorbic acid (AsA)) is crucial for human health and wellbeing and thus increasing AsA content is of interest to plant breeders. In plants GDP-l-galactose phosphorylase (GGP) is a key biosynthetic control step and here evidence is presented for two new transcriptional activators of GGP. AsA measurement, transcriptomics, transient expression, hormone application, gene editing, yeast 1/2-hybrid, and electromobility shift assay (EMSA) methods were used to identify two positively regulating transcription factors. AceGGP3 was identified as the most highly expressed GGP in Actinidia eriantha fruit, which has high fruit AsA. A gene encoding a 1R-subtype myeloblastosis (MYB) protein, AceMYBS1, was found to bind the AceGGP3 promoter and activate its expression. Overexpression and gene-editing show AceMYBS1 effectively increases AsA accumulation. The bZIP transcription factor AceGBF3 (a G-box binding factor), also was shown to increase AsA content, and was confirmed to interact with AceMYBS1. Co-expression experiments showed that AceMYBS1 and AceGBF3 additively promoted AceGGP3 expression. Furthermore, AceMYBS1, but not GBF3, was repressed by abscisic acid, resulting in reduced AceGGP3 expression and accumulation of AsA. This study sheds new light on the roles of MYBS1 homologues and ABA in modulating AsA synthesis, and adds to the understanding of mechanisms underlying AsA accumulation.
植物源性维生素 C(L-抗坏血酸(AsA))对人类健康和幸福至关重要,因此提高 AsA 含量是植物育种者感兴趣的。在植物中,GDP-L-半乳糖磷酸化酶(GGP)是一个关键的生物合成控制步骤,这里提出了两个新的 GGP 转录激活因子的证据。使用 AsA 测量、转录组学、瞬时表达、激素应用、基因编辑、酵母 1/2-杂交和电泳迁移率变动分析(EMSA)方法来鉴定两个正向调节转录因子。AceGGP3 被鉴定为 Actinidia eriantha 果实中表达量最高的 GGP,其果实中 AsA 含量高。发现一个编码 1R 型髓样细胞瘤(MYB)蛋白的基因 AceMYBS1,结合 AceGGP3 启动子并激活其表达。过表达和基因编辑表明 AceMYBS1 可有效增加 AsA 积累。bZIP 转录因子 AceGBF3(G 框结合因子)也被证明能增加 AsA 含量,并被证实与 AceMYBS1 相互作用。共表达实验表明,AceMYBS1 和 AceGBF3 可累加促进 AceGGP3 表达。此外,AceMYBS1(而非 GBF3)被脱落酸抑制,导致 AceGGP3 表达减少和 AsA 积累减少。本研究揭示了 MYBS1 同源物和 ABA 在调节 AsA 合成中的作用,增加了对 AsA 积累机制的理解。