作者 Tu, Lichan; Su, Ping; Zhang, Zhongren; Gao, Linhui; Wang, Jiadian; Hu, Tianyuan; Zhou, Jiawei; Zhang, Yifeng; Zhao, Yujun; Liu, Yuan; Song, Yadi; Tong, Yuru; Lu, Yun; Yang, Jian; Xu, Cao; Jia, Meirong; Peters, Reuben J.; Huang, Luqi; Gao, Wei
期刊 NATURE COMMUNICATIONS , FEB 20 2020,1:11
DOI 10.1038/s41467-020-14776-1 PubMed 32080175
摘要 Triptolide is a trace natural product of Tripterygium wilfordii. It has antitumor activities, particularly against pancreatic cancer cells. Identification of genes and elucidation of the biosynthetic pathway leading to triptolide are the prerequisite for heterologous bioproduction. Here, we report a reference-grade genome of T. wilfordii with a contig N50 of 4.36 Mb. We show that copy numbers of triptolide biosynthetic pathway genes are impacted by a recent whole-genome triplication event. We further integrate genomic, transcriptomic, and metabolomic data to map a gene-to-metabolite network. This leads to the identification of a cytochrome P450 (CYP728B70) that can catalyze oxidation of a methyl to the acid moiety of dehydroabietic acid in triptolide biosynthesis. We think the genomic resource and the candidate genes reported here set the foundation to fully reveal triptolide biosynthetic pathway and consequently the heterologous bioproduction.Tripterygium wilfordii is a medical plant that can produce antitumor activity compound triptolide. Here, the authors assemble its genome and identify a cytochrome P450 that can catalyze oxidation of a methyl to the acid moiety of dehydroabietic acid in triptolide biosynthesis by integrating multi-omics data.
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