College of Biological Sciences & Engineering, Shaanxi University of Technology, Hanzhong, 723001, China.
Institute of Soil and Water Conservation, CAS & MWR, Yangling, 712100, China; University of Chinese Academy of Sciences, Beijing, 100049, China.
Phytochemistry. 2020 Jan;169:112183. doi: 10.1016/j.phytochem.2019.112183. Epub 2019 Nov 6.
Phenolic acids and tanshinones are the two groups of pharmaceutically active metabolites in Salvia miltiorrhiza Bunge. Their contents are the key quality indicator to evaluate S. miltiorrhiza. bHLH transcription factors have important roles in regulation of plant specialised metabolism. In this study, an endogenous bHLH transcription factor, SmbHLH3, was identified and functionally analyzed. SmbHLH3 was presented in all the six tissues and mostly expressed in fibrous roots and flowers. It was localized to the nucleus. Overexpression of SmbHLH3 decreased both phenolic acids and tanshinones contents. Contents of caffeic acid and rosmarinic acid were both decreased to 50% of the control. And accumulation of salvianolic acid B was decreased as much as 62%. Content of cryptotanshinone, dihydrotanshinone I, tanshinone I and tanshinone IIA in SmbHLH3-overexpression lines were reduced 97%, 62%, 86% and 91%, respectively. In the transgenic lines, expression of C4H1, TAT and HPPR in phenolic acids pathways were reduced to about 43%, 66% and 77% of the control, respectively. For tanshinone biosynthetic pathways, transcripts of DXS3, DXR, HMGR1, KSL1, CPS1 and CYP76AH1 were reduced to 46%, 65%, 78%, 57%, 27% and 62% of the control, respectively. There was an E/G-box specific binding site in SmbHLH3, which may bind the E/G-box present in promoter region of these biosynthetic pathway genes. Y1H results indicated that SmbHLH3 could bind the promoter of TAT, HPPR, KSL1 and CYP76AH1. These findings indicated that SmbHLH3 downregulate both phenolic acids and tanshinone accumulation through directly suppressing the transcription of key enzyme genes.
丹酚酸和丹参酮是丹参中的两类具有药用活性的代谢产物。它们的含量是评价丹参质量的关键指标。bHLH 转录因子在植物特化代谢的调控中具有重要作用。本研究鉴定并分析了一个内源性 bHLH 转录因子 SmbHLH3。SmbHLH3 在所有 6 种组织中均有表达,在纤维根和花中表达量最高。该蛋白定位于细胞核。过表达 SmbHLH3 导致丹酚酸和丹参酮含量均降低。咖啡酸和迷迭香酸的含量分别降至对照的 50%。丹酚酸 B 的积累减少了 62%。SmHLH3 过表达系中隐丹参酮、二氢丹参酮 I、丹参酮 I 和丹参酮 IIA 的含量分别降低了 97%、62%、86%和 91%。在转基因系中,C4H1、TAT 和 HPPR 在丹酚酸途径中的表达分别降至对照的 43%、66%和 77%左右。对于丹参酮生物合成途径,DXS3、DXR、HMGR1、KSL1、CPS1 和 CYP76AH1 的转录本分别减少到对照的 46%、65%、78%、57%、27%和 62%。SmbHLH3 中有一个 E/G 盒特异结合位点,可能与这些生物合成途径基因启动子区的 E/G 盒结合。Y1H 结果表明,SmbHLH3 可以结合 TAT、HPPR、KSL1 和 CYP76AH1 启动子。这些结果表明,SmbHLH3 通过直接抑制关键酶基因的转录,下调丹酚酸和丹参酮的积累。