Key Laboratory of Cultivation and Protection for Non-Wood Forest Trees of Ministry of Education, Central South University of Forestry and Technology, Changsha 410004, China.
Key Laboratory of Non-Wood Forest Products of State Forestry Administration, Central South University of Forestry and Technology, Changsha 410004, China.
Int J Mol Sci. 2024 Oct 17;25(20):11134. doi: 10.3390/ijms252011134.
Squalene synthase (SQS) is the most direct key enzyme regulating squalene synthesis. To better understand the regulatory mechanisms of squalene biosynthesis, a 1423-bp long promoter region of the gene was isolated from . Plant CARE and PLACE analysis affirmed the existence of the core promoter elements such as TATA and CAAT boxes and transcription factor binding sites like W-box and MYB in the isolated sequence. Exogenous factors regulating the promoter were obtained by using Yeast one-hybrid screening, and the key transcription factor CoWRKY15 was found. AOS (Antibody Optimization System) analysis showed that CoWRKY15 had the highest interactions with a confidence level of 0.9026. Bioinformatics analysis showed that CoWRKY15 belonged to class 2 of the gene family. The results of subcellular localization showed that CoWRKY15 functioned in the nucleus. The results of CoWRKY15 promoter analysis showed that 8 out of 14 cis-elements with annotatable functions were related to the light response. The region of the promoter that interacts with CoWRKY15 is -186 bp-536 bp. The histochemical assay and squalene content suggested that the promoter could drive the expression of GUS gene and specific promotion of expression. It was found that CoWRKY15 could act on the -186 bp-536 bp promoter to regulate the expression of and the content of squalene in seed kernels.
鲨烯合酶(SQS)是调节鲨烯合成的最直接的关键酶。为了更好地理解鲨烯生物合成的调控机制,从 中分离出了 基因的 1423bp 长启动子区域。植物 CARE 和 PLACE 分析证实了在分离的序列中存在 TATA 和 CAAT 盒等核心启动子元件以及 W-box 和 MYB 等转录因子结合位点。通过酵母单杂交筛选获得了调节 启动子的外源因子,并发现了关键转录因子 CoWRKY15。AOS(抗体优化系统)分析表明,CoWRKY15 与具有 0.9026 置信水平的抗体具有最高的相互作用。生物信息学分析表明,CoWRKY15 属于 基因家族的第 2 类。亚细胞定位结果表明 CoWRKY15 在细胞核中起作用。CoWRKY15 启动子分析结果表明,具有可注释功能的 14 个顺式元件中有 8 个与光反应有关。与 CoWRKY15 相互作用的 启动子区域为-186bp-536bp。组织化学检测和鲨烯含量表明,该启动子可以驱动 GUS 基因的表达,并特异性促进 基因的表达。研究发现 CoWRKY15 可以作用于-186bp-536bp 的 启动子,调节 基因的表达和种子仁中鲨烯的含量。