Zhao Xuecheng, Zeng Xiangsheng, Lin Ning, Yu Shuwei, Fernie Alisdair R, Zhao Jian
State Key Laboratory of Tea Plant Biology and Utilization, Anhui Agricultural University, 230036, Hefei, China.
College of Agronomy, Anhui Agricultural University, 230036, Hefei, China.
Hortic Res. 2021 May 1;8(1):110. doi: 10.1038/s41438-021-00545-8.
Under high light conditions or UV radiation, tea plant leaves produce more flavonols, which contribute to the bitter taste of tea; however, neither the flavonol biosynthesis pathways nor the regulation of their production are well understood. Intriguingly, tea leaf flavonols are enhanced by UV-B but reduced by shading treatment. CsFLS, CsUGT78A14, CsMYB12, and CsbZIP1 were upregulated by UV-B radiation and downregulated by shading. CsMYB12 and CsbZIP1 bound to the promoters of CsFLS and CsUGT78A14, respectively, and activated their expression individually. CsbZIP1 positively regulated CsMYB12 and interacted with CsMYB12, which specifically activated flavonol biosynthesis. Meanwhile, CsPIF3 and two MYB repressor genes, CsMYB4 and CsMYB7, displayed expression patterns opposite to that of CsMYB12. CsMYB4 and CsMYB7 bound to CsFLS and CsUGT78A14 and repressed their CsMYB12-activated expression. While CsbZIP1 and CsMYB12 regulated neither CsMYB4 nor CsMYB7, CsMYB12 interacted with CsbZIP1, CsMYB4, and CsMYB7, but CsbZIP1 did not physically interact with CsMYB4 or CsMYB7. Finally, CsPIF3 bound to and activated CsMYB7 under shading to repress flavonol biosynthesis. These combined results suggest that UV activation and shading repression of flavonol biosynthesis in tea leaves are coordinated through a complex network involving CsbZIP1 and CsPIF3 as positive MYB activators and negative MYB repressors, respectively. The study thus provides insight into the regulatory mechanism underlying the production of bitter-tasting flavonols in tea plants.
在高光条件或紫外线辐射下,茶树叶片会产生更多的黄酮醇,这导致了茶叶的苦味;然而,黄酮醇的生物合成途径及其产生的调控机制尚未得到充分了解。有趣的是,UV-B可增强茶叶黄酮醇含量,而遮荫处理则会降低其含量。UV-B辐射可上调CsFLS、CsUGT78A14、CsMYB12和CsbZIP1的表达,而遮荫处理则使其下调。CsMYB12和CsbZIP1分别与CsFLS和CsUGT78A14的启动子结合,并分别激活它们的表达。CsbZIP1正向调控CsMYB12,并与CsMYB12相互作用,特异性激活黄酮醇生物合成。同时,CsPIF3以及两个MYB抑制基因CsMYB4和CsMYB7的表达模式与CsMYB12相反。CsMYB4和CsMYB7与CsFLS和CsUGT78A14结合,并抑制CsMYB12激活的它们的表达。虽然CsbZIP1和CsMYB12对CsMYB4和CsMYB7均无调控作用,但CsMYB12与CsbZIP1、CsMYB4和CsMYB7相互作用,而CsbZIP1与CsMYB4或CsMYB7无直接物理相互作用。最后,CsPIF3在遮荫条件下与CsMYB7结合并激活其表达,从而抑制黄酮醇生物合成。这些综合结果表明,茶树叶片中黄酮醇生物合成的紫外线激活和遮荫抑制是通过一个复杂的网络协调进行的,其中CsbZIP1和CsPIF3分别作为正向MYB激活因子和负向MYB抑制因子。该研究为茶树中苦味黄酮醇产生的调控机制提供了见解。