Sequencing of Panax notoginseng genome reveals genes involved in disease resistance and ginsenoside biosynthesis
Guangyi FaniD, Yuanyuan FuiD, Binrui YangiD, Minghua LiuiD, He ZhangiD, Xinming LiangiD, Chengcheng ShiiD, Kailong MaiD, Jiahao WangiD, Weiqing LiuiD, Libin ShaoiD, Chen HuangiD, Min GuoiD, Jing CaiiD, Andrew K. C. WongiD, Cheuk‐Wing LiiD, Dennis Zhuang, Keji CheniD, Weihong CongiD, Xiao Song SuniD, Wenbin CheniD, Xun XuiD, Stephen Kwok‐Wing TsuiiD, Xin LiuiD, Simon Ming‐Yuen LeeiD
Abstract
Panax notoginseng is a traditional Chinese herb with high medicinal and economic value. There has been considerable research on the pharmacological activities of ginsenosides contained in Panax spp.; however, very little is known about the ginsenoside biosynthetic pathway. We reported the first de novo genome of 2.36 Gb of sequences from P. notoginseng with 35,451 protein-encoding genes. Compared to other plants, we found notable gene family contraction of disease-resistance genes in P. notoginseng, but notable expansion for several ATP-binding cassette (ABC) transporter subfamilies, such as the Gpdr subfamily, indicating that ABCs might be an additional mechanism for the plant to cope with biotic stress. Combining eight transcriptomes of roots and aerial parts, we identified several key genes, their transcription factor binding sites and all their family members involved in the synthesis pathway of ginsenosides in P. notoginseng, including dammarenediol synthase, CYP716 and UGT71. The complete genome analysis of P. notoginseng, the first in genus Panax, will serve as an important reference sequence for improving breeding and cultivation of this important nutraceutical and medicinal but vulnerable plant species.
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