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Jasmonate promotes artemisinin biosynthesis by activating the TCP14-ORA complex in Artemisia annua

Artemisia annua produces the valuable medicinal component, artemisinin, which is a sesquiterpene lactone widely used in malaria treatment. AaORA, a homolog of CrORCA3, which is involved in activating terpenoid indole alkaloid biosynthesis in Catharanthus roseus, is a jasmonate (JA)–responsive and tr...

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Detalles Bibliográficos
Autores principales: Ma, Ya-Nan, Xu, Dong-Bei, Li, Ling, Zhang, Fei, Fu, Xue-Qing, Shen, Qian, Lyu, Xue-Ying, Wu, Zhang-Kuanyu, Pan, Qi-Fang, Shi, Pu, Hao, Xiao-Long, Yan, Ting-Xiang, Chen, Ming-Hui, Liu, Pin, He, Qian, Xie, Li-Hui, Zhong, Yi-Jun, Tang, Yue-Li, Zhao, Jing-Ya, Zhang, Li-Da, Sun, Xiao-Fen, Tang, Ke-Xuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6317983/
https://www.ncbi.nlm.nih.gov/pubmed/30627665
http://dx.doi.org/10.1126/sciadv.aas9357
Descripción
Sumario:Artemisia annua produces the valuable medicinal component, artemisinin, which is a sesquiterpene lactone widely used in malaria treatment. AaORA, a homolog of CrORCA3, which is involved in activating terpenoid indole alkaloid biosynthesis in Catharanthus roseus, is a jasmonate (JA)–responsive and trichome-specific APETALA2/ETHYLENE-RESPONSE FACTOR that plays a pivotal role in artemisinin biosynthesis. However, the JA signaling mechanism underlying AaORA-mediated artemisinin biosynthesis remains enigmatic. Here, we report that AaORA forms a transcriptional activator complex with AaTCP14 (TEOSINTE BRANCHED 1/CYCLOIDEA/PROLIFERATING CELL FACTOR 14), which is also predominantly expressed in trichomes. AaORA and AaTCP14 synergistically bind to and activate the promoters of two genes, double bond reductase 2 (DBR2) and aldehyde dehydrogenase 1 (ALDH1), both of which encode enzymes vital for artemisinin biosynthesis. AaJAZ8, a repressor of the JA signaling pathway, interacts with both AaTCP14 and AaORA and represses the ability of the AaTCP14-AaORA complex to activate the DBR2 promoter. JA treatment induces AaJAZ8 degradation, allowing the AaTCP14-AaORA complex to subsequently activate the expression of DBR2, which is essential for artemisinin biosynthesis. These data suggest that JA activation of the AaTCP14-AaORA complex regulates artemisinin biosynthesis. Together, our findings reveal a novel artemisinin biosynthetic pathway regulatory network and provide new insight into how specialized metabolism is modulated by the JA signaling pathway in plants.