National Engineering Laboratory for Resource Development of Endangered Crude Drugs in Northwest of China, Key Laboratory of the Ministry of Education for Medicinal Resources and Natural Pharmaceutical Chemistry, Shaanxi Normal University, 710062 Xi'an, China.
School of Landscape and Ecological Engineering, Hebei University of Engineering, 056038 Handan, China.
Gene. 2020 Sep 25;756:144920. doi: 10.1016/j.gene.2020.144920. Epub 2020 Jun 25.
Basic helix-loop-helix (bHLH) transcription factors play essential roles in myriad regulatory processes, including secondary metabolism. In this study with Salvia miltiorrhiza, we isolated and characterized SmbHLH53, which encodes a bHLH family member. Expression of this gene was significantly induced by wounding and multiple hormones, including methyl jasmonic acid; transcript levels were highest in the leaves and roots. Phylogenetic analysis indicated that SmbHLH53 clusters withAtbHLH17 and AtbHLH13, two negative regulators of jasmonate (JA) responses, and is localized in the nucleus and cell membrane. Yeast two-hybrid and bimolecular fluorescent complementation assays indicated that SmbHLH53 forms a homodimer as well as a heterodimer with SmbHLH37. It also interacts with both SmJAZs1/3/8 and SmMYC2, the core members of the JA signal pathway. Unexpectedly, we noted that overexpression of SmbHLH53 did not significantly influence the concentrations of rosmarinic acid and salvianolic acid B in transgenic plants. Results from yeast one-hybrid assays showed that SmbHLH53 binds to the promoters of SmTAT1, SmPAL1, and Sm4CL9, the key genes for enzymes in the pathway for phenolic acid synthesis. Assays of transient transcriptional activity demonstrated that SmbHLH53 represses the promoter of SmTAT1 while activating the promoter of Sm4CL9. Thus, the present work revealed that SmbHLH53 may play dual roles in regulating the genes for enzymes in the pathway for Sal B biosynthesis.
碱性螺旋-环-螺旋(bHLH)转录因子在众多调节过程中发挥着重要作用,包括次生代谢。在这项对丹参的研究中,我们分离并鉴定了 SmbHLH53,它编码 bHLH 家族成员。该基因的表达受到创伤和多种激素的显著诱导,包括茉莉酸甲酯;转录水平在叶片和根中最高。系统发育分析表明,SmbHLH53 与 AtbHLH17 和 AtbHLH13 聚类,AtbHLH17 和 AtbHLH13 是茉莉酸(JA)反应的负调节剂,定位于细胞核和细胞膜中。酵母双杂交和双分子荧光互补测定表明,SmbHLH53 形成同源二聚体以及与 SmbHLH37 的异源二聚体。它还与 SmJAZs1/3/8 和 SmMYC2 相互作用,SmJAZs1/3/8 和 SmMYC2 是 JA 信号通路的核心成员。出乎意料的是,我们注意到 SmbHLH53 的过表达并没有显著影响转基因植物中迷迭香酸和丹酚酸 B 的浓度。酵母单杂交试验的结果表明,SmbHLH53 结合到 SmTAT1、SmPAL1 和 Sm4CL9 的启动子上,SmTAT1、SmPAL1 和 Sm4CL9 是酚酸合成途径中酶的关键基因。瞬时转录活性测定表明,SmbHLH53 抑制 SmTAT1 启动子而激活 Sm4CL9 启动子。因此,本研究表明 SmbHLH53 可能在调节丹酚酸 B 生物合成途径中酶的基因方面发挥双重作用。