J Agric Food Chem. 2018 Oct 31;66(43):11234-11243. doi: 10.1021/acs.jafc.8b02175. Epub 2018 Oct 23.
Tea O-methylated catechins, especially (-)-epigallocatechin 3- O-(3- O-methyl)gallate (EGCG3″Me), have been attracting much attention as a result of their positive health effects. The transcription regulators of O-methylated catechin biosynthesis remain elusive. In this study, the expression pattern of genes related to O-methylated catechin biosynthesis, including CsLAR, CsANS, CsDFR, CsANR, and CCoAOMT, in three tea cultivars with different contents of EGCG3″Me was investigated. Two WRKY transcription factors (TFs), designated as CsWRKY31 and CsWRKY48, belonging to groups IIb and IIc of the WRKY family, respectively, were further identified. CsWRKY31 and CsWRKY48 were nuclear-localized proteins and possessed transcriptional repression ability. Furthermore, expression of CsWRKY31 and CsWRKY48 showed negative correlation with CsLAR, CsDFR, and CCoAOMT during EGCG3″Me accumulation in tea leaves. More importantly, W-box (C/T)TGAC(T/C) elements were located in the promoter of CsLAR, CsDFR, and CCoAOMT, and further assays revealed that CsWRKY31 and CsWRKY48 were capable of repressing the transcription of CsLAR, CsDFR, and CCoAOMT via the attachment of their promoters to the W-box elements. Collectively, our findings identify two novel negative regulators of O-methylated catechin biosynthesis in tea plants, which might provide a potential strategy to breed high-quality tea cultivar.
茶甲基化儿茶素,尤其是(-)-表没食子儿茶素 3-O-(3-O-甲基)没食子酸酯(EGCG3″Me),由于其对健康的积极影响而备受关注。甲基化儿茶素生物合成的转录调控因子仍难以捉摸。在这项研究中,研究了三个 EGCG3″Me 含量不同的茶树品种中与甲基化儿茶素生物合成相关的基因(包括 CsLAR、CsANS、CsDFR、CsANR 和 CCoAOMT)的表达模式。进一步鉴定了两个 WRKY 转录因子(TFs),分别命名为 CsWRKY31 和 CsWRKY48,它们分别属于 WRKY 家族的 IIb 和 IIc 组。CsWRKY31 和 CsWRKY48 是核定位蛋白,具有转录抑制能力。此外,在茶树叶片 EGCG3″Me 积累过程中,CsWRKY31 和 CsWRKY48 的表达与 CsLAR、CsDFR 和 CCoAOMT 呈负相关。更重要的是,W 框(C/T)TGAC(T/C)元件位于 CsLAR、CsDFR 和 CCoAOMT 的启动子中,进一步的实验表明,CsWRKY31 和 CsWRKY48 能够通过将其启动子附着在 W 框元件上来抑制 CsLAR、CsDFR 和 CCoAOMT 的转录。总之,我们的研究结果确定了茶树中甲基化儿茶素生物合成的两个新的负调控因子,这可能为培育优质茶树品种提供了一种潜在的策略。