Yang Zhirong, Patra Barunava, Li Runzhi, Pattanaik Sitakanta, Yuan Ling
Institute of Molecular Agriculture and Bioenergy, Shanxi Agricultural University, Taigu, 030801, Shanxi, China.
Department of Biochemistry, College of Arts and Sciences, Shanxi Agricultural University, Taigu, 030801, Shanxi, China.
Planta. 2013 Dec;238(6):1039-49. doi: 10.1007/s00425-013-1949-2. Epub 2013 Aug 27.
WRKY transcription factors (TFs) are emerging as an important group of regulators of plant secondary metabolism. However, the cis-regulatory elements associated with their regulation have not been well characterized. We have previously demonstrated that CrWRKY1, a member of subgroup III of the WRKY TF family, regulates biosynthesis of terpenoid indole alkaloids in the ornamental and medicinal plant, Catharanthus roseus. Here, we report the isolation and functional characterization of the CrWRKY1 promoter. In silico analysis of the promoter sequence reveals the presence of several potential TF binding motifs, indicating the involvement of additional TFs in the regulation of the TIA pathway. The CrWRKY1 promoter can drive the expression of a β-glucuronidase (GUS) reporter gene in native (C. roseus protoplasts and transgenic hairy roots) and heterologous (transgenic tobacco seedlings) systems. Analysis of 5'- or 3'-end deletions indicates that the sequence located between positions -140 to -93 bp and -3 to +113 bp, relative to the transcription start site, is critical for promoter activity. Mutation analysis shows that two overlapping as-1 elements and a CT-rich motif contribute significantly to promoter activity. The CrWRKY1 promoter is induced in response to methyl jasmonate (MJ) treatment and the promoter region between -230 and -93 bp contains a putative MJ-responsive element. The CrWRKY1 promoter can potentially be used as a tool to isolate novel TFs involved in the regulation of the TIA pathway.
WRKY转录因子正逐渐成为植物次生代谢的重要调控因子组。然而,与其调控相关的顺式调控元件尚未得到充分表征。我们之前已经证明,CrWRKY1是WRKY转录因子家族III亚组的成员,可调控观赏和药用植物长春花中萜类吲哚生物碱的生物合成。在此,我们报告了CrWRKY1启动子的分离和功能表征。对启动子序列的电子分析揭示了几个潜在的转录因子结合基序的存在,表明其他转录因子参与了萜类吲哚生物碱途径的调控。CrWRKY1启动子可在天然(长春花原生质体和转基因毛状根)和异源(转基因烟草幼苗)系统中驱动β-葡萄糖醛酸酶(GUS)报告基因的表达。对5'或3'末端缺失的分析表明,相对于转录起始位点,位于-140至-93 bp和-3至+113 bp位置之间的序列对启动子活性至关重要。突变分析表明,两个重叠的as-1元件和一个富含CT的基序对启动子活性有显著贡献。CrWRKY1启动子在茉莉酸甲酯(MJ)处理后被诱导,并且-230至-93 bp之间的启动子区域包含一个假定的MJ响应元件。CrWRKY1启动子有可能用作分离参与萜类吲哚生物碱途径调控的新型转录因子的工具。