Key Laboratory of Horticultural Plant Biology (HZAU), MOE, Huazhong Agricultural University, Wuhan, 430070, China.
Southwest Research Center for Engineering Technology of Landscape Architecture (State Forestry Administration), Southwest Forestry University, Kunming, 650224, China.
Plant Cell Rep. 2020 Jul;39(7):891-907. doi: 10.1007/s00299-020-02537-9. Epub 2020 Apr 24.
Overexpression of CpbHLH1 in Arabidopsis and tobacco resulted in a dramatic decrease in anthocyanin accumulation by repressing the expression of late biosynthesis genes in the flavonoid biosynthesis pathway. Many basic helix-loop-helix (bHLH) transcription factors (TFs) of subgroup IIIf have been characterized as anthocyanin-associated activators in higher plants, but information regarding bHLH TFs that inhibit anthocyanin accumulation remains scarce. In this study, the subgroup IIIf bHLH TF CpbHLH1 from Chimonanthus praecox (L.) was identified as a negative regulator of anthocyanin accumulation. Our results showed that overexpression of CpbHLH1 in model plant species, Arabidopsis and tobacco, resulted in a dramatic decrease in anthocyanin content, whereas the content of proanthocyanidin was little affected. Quantitative RT-PCR (qRT-PCR) assays of the structural genes in the flavonoid biosynthesis pathway revealed that CpbHLH1 inhibits anthocyanin accumulation mainly through repressing the expression of late biosynthesis genes (LBGs). Interactions between CpbHLH1 protein and AtPAP1/NtAN2 protein were detected via yeast two-hybrid (Y2H) and bimolecular fluorescence complementation (BiFC) assays. This is the first bHLH repressor of anthocyanin biosynthesis identified in dicotyledons. These results can help us better understand the anthocyanin regulatory network in plants and may provide insights into the diverse functions of bHLH proteins.
CpbHLH1 在拟南芥和烟草中的过表达导致类黄酮生物合成途径中晚期生物合成基因的表达受到抑制,从而导致花青素积累显著减少。许多亚组 IIIf 的碱性螺旋-环-螺旋(bHLH)转录因子(TFs)已被鉴定为高等植物中与花青素相关的激活子,但关于抑制花青素积累的 bHLH TF 的信息仍然很少。在这项研究中,从蜡梅(Chimonanthus praecox(L.))中鉴定出亚组 IIIf bHLH TF CpbHLH1 是花青素积累的负调控因子。我们的结果表明,CpbHLH1 在模式植物拟南芥和烟草中的过表达导致花青素含量显著下降,而原花青素的含量几乎没有受到影响。类黄酮生物合成途径结构基因的定量 RT-PCR(qRT-PCR)分析表明,CpbHLH1 通过抑制晚期生物合成基因(LBGs)的表达来抑制花青素的积累。酵母双杂交(Y2H)和双分子荧光互补(BiFC)实验检测到 CpbHLH1 蛋白与 AtPAP1/NtAN2 蛋白之间的相互作用。这是在双子叶植物中鉴定的第一个花青素生物合成的 bHLH 抑制剂。这些结果可以帮助我们更好地理解植物中花青素的调控网络,并为 bHLH 蛋白的多种功能提供见解。