Deng Yin-Ai, Li Li, Peng Qian, Feng Ling-Fang, Yang Jin-Fen, Zhan Ruo-Ting, Ma Dong-Ming
Research Center of Chinese Herbal Resource Science and Engineering, Guangzhou University of Chinese Medicine, Key Laboratory of Chinese Medicinal Resource from Lingnan (Guangzhou University of Chinese Medicine), Ministry of Education, Joint Laboratory of National Engineering Research Center for the Pharmaceutics of Traditional Chinese Medicines, Guangzhou, 510006, People's Republic of China.
Planta. 2022 May 12;255(6):122. doi: 10.1007/s00425-022-03892-5.
AaZFP1, a C2H2-type transcription factor, was found to bind the AGT-N1-10-AGT box of AaIPPI1pro and activate the expression of AaIPPI1 involved in artemisinin biosynthesis. Artemisinin, an endoperoxide sesquiterpene lactone, is a widely used antimalarial drug isolated from Artemisia annua L. Isopentenyl pyrophosphate isomerase (AaIPPI1) catalyzes the interconversion of isopentenyl diphosphate and dimethylallyl diphosphate and is the key gene involved in the biosynthesis of artemisinin. However, the AaIPPI1 gene regulation network remains largely unknown. Here, we isolated the AaIPPI1 promoter (AaIPPI1pro) and predicted that it contains cis-elements involved in stress responses, including the TGACG motif (a methyl jasmonate-responsive element), GARE motif (a gibberellin-responsive element), ABRE (an abscisic acid-responsive element), TC-rich repeats (a stress-responsive element), and the AGT-N-AGT box, which is the binding site of Cys/His2 zinc finger protein (C2H2 ZFP). The C2H2 ZFP gene AaZFP1 was discovered by screening a cDNA library using AaIPPI1pro as bait in yeast. AaZFP1 contains two conserved C2H2 regions, a nuclear localization domain (B box), a Leu-rich domain (L box), and a conserved DLN sequence (DLN box) close to its C terminus. A subcellular localization assay indicated that AaZFP1 protein is localized in the nucleus and cytoplasm. An electrophoretic mobility shift assay demonstrated that AaZFP1 binds to the AGT-N-AGT box of AaIPPI1pro. A dual-luciferase assay indicated that AaZFP1 enhanced the promoter activity of AaIPPI1 in vivo. Transient overexpression of AaZFP1 in A. annua increased the expression of AaIPPI1 and the content of artemisinin. Our data demonstrated that AaZFP1 functions as a transcriptional activator that regulates the expression of AaIPPI1 by directly binding to its promoter. The present study provides insights into the transcriptional regulation of genes involved in artemisinin biosynthesis in A. annua.
AaZFP1是一种C2H2型转录因子,被发现可与AaIPPI1pro的AGT-N1-10-AGT框结合,并激活参与青蒿素生物合成的AaIPPI1的表达。青蒿素是一种内过氧化物倍半萜内酯,是从黄花蒿中分离出的一种广泛使用的抗疟药物。异戊烯基焦磷酸异构酶(AaIPPI1)催化异戊烯基二磷酸和二甲基烯丙基二磷酸的相互转化,是参与青蒿素生物合成的关键基因。然而,AaIPPI1基因调控网络在很大程度上仍然未知。在此,我们分离出了AaIPPI1启动子(AaIPPI1pro),并预测它含有参与应激反应的顺式元件,包括TGACG基序(茉莉酸甲酯反应元件)、GARE基序(赤霉素反应元件)、ABRE(脱落酸反应元件)、富含TC的重复序列(应激反应元件)以及AGT-N-AGT框,后者是Cys/His2锌指蛋白(C2H2 ZFP)的结合位点。通过在酵母中以AaIPPI1pro为诱饵筛选cDNA文库,发现了C2H2 ZFP基因AaZFP1。AaZFP1包含两个保守的C2H2区域、一个核定位结构域(B框)、一个富含亮氨酸的结构域(L框)以及靠近其C末端的一个保守的DLN序列(DLN框)。亚细胞定位分析表明,AaZFP1蛋白定位于细胞核和细胞质中。电泳迁移率变动分析表明,AaZFP1与AaIPPI1pro的AGT-N-AGT框结合。双荧光素酶分析表明,AaZFP1在体内增强了AaIPPI1的启动子活性。在黄花蒿中瞬时过表达AaZFP1可增加AaIPPI1的表达以及青蒿素的含量。我们的数据表明,AaZFP1作为一种转录激活因子,通过直接结合其启动子来调控AaIPPI1的表达。本研究为黄花蒿中参与青蒿素生物合成的基因的转录调控提供了见解。