School of Biological Sciences, University of Auckland, 3 Symonds Street, Auckland, New Zealand.
The New Zealand Institute for Plant and Food Research Limited, 120 Mt Albert Road, Auckland, New Zealand.
Sci Rep. 2020 Aug 25;10(1):14161. doi: 10.1038/s41598-020-70977-0.
The groups of plant flavonoid metabolites termed anthocyanins and proanthocyanins (PA) are responsible for pigmentation in seeds, flowers and fruits. Anthocyanins and PAs are produced by a pathway of enzymes which are transcriptionally regulated by transcription factors (TFs) that form the MYB-bHLH-WD40 (MBW) complex. In this study, transcriptomic analysis of purple-pigmented kiwifruit skin and flesh tissues identified MYBC1, from subgroup 5 of the R2R3 MYB family, and WRKY44 (highly similar to Arabidopsis TTG2) as candidate activators of the anthocyanin pathway. Transient over-expression of MYBC1 and WRKY44 induced anthocyanin accumulation in tobacco leaves. Dual luciferase promoter activation assays revealed that both MYBC1 and WRKY44 were able to strongly activate the promoters of the kiwifruit F3'H and F3'5'H genes. These enzymes are branch points of the pathway which specifies the type of anthocyanin accumulated. Stable over-expression of MYBC1 and WRKY44 in kiwifruit calli activated the expression of F3'5'H and PA-related biosynthetic genes as well as increasing levels of PAs. These results suggest that while previously characterised anthocyanin activator MYBs regulate the overall anthocyanin biosynthesis pathway, the PA-related TFs, MYBC1 and WRKY44, more specifically regulate key branch points. This adds a layer of regulatory control that potentially balances anthocyanin and PA levels.
植物类黄酮代谢物群体,如花色苷和原花色素(PA),负责种子、花朵和果实的色素形成。花色苷和 PAs 是由一系列酶的途径产生的,这些酶的转录受到转录因子(TFs)的转录调控,这些 TFs 形成 MYB-bHLH-WD40(MBW)复合物。在这项研究中,对紫色着色猕猴桃果皮和果肉组织的转录组分析鉴定了 R2R3 MYB 家族亚组 5 中的 MYBC1 和 WRKY44(与拟南芥 TTG2 高度相似)作为花色苷途径的候选激活子。MYBC1 和 WRKY44 的瞬时过表达诱导了烟草叶片中的花色苷积累。双荧光素酶启动子激活测定表明,MYBC1 和 WRKY44 均能够强烈激活猕猴桃 F3'H 和 F3'5'H 基因的启动子。这些酶是指定积累花色苷类型的途径的分支点。MYBC1 和 WRKY44 在猕猴桃愈伤组织中的稳定过表达激活了 F3'5'H 和 PA 相关生物合成基因的表达,并增加了 PA 的水平。这些结果表明,虽然先前表征的花色苷激活 MYB 调节整体花色苷生物合成途径,但 PA 相关的 TFs,如 MYBC1 和 WRKY44,更具体地调节关键分支点。这增加了一层潜在的调节控制,可能平衡花色苷和 PA 的水平。