Huo Jinxi, Zhong Shi, Du Xin, Cao Yinglong, Wang Wenqiong, Sun Yuqing, Tian Yu, Zhu Jianxun, Chen Jine, Xuan Lijiang, Wu Chongming, Li Yougui
Sericultural Research Institute, Zhejiang Academy of Agricultural Sciences, Hangzhou 310021, People's Republic of China.
State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 201203, People's Republic of China.
J Adv Res. 2020 Apr 28;24:325-335. doi: 10.1016/j.jare.2020.04.011. eCollection 2020 Jul.
(Schwein.) Pat, a species of 'Sanghuang', has been well-documented for various medicinal uses, but the genome information and active constituents are largely unknown. Here, we sequenced the whole-genome of , identified phenylpropanoids as its key anti-cancer components, and deduced their biosynthesis pathways. A 41.11-Mb genome sequence was assembled and the heatmap created with high-throughput chromosome conformation capture techniques data suggested all bins could be clearly divided into 11 pseudochromosomes. Cellular experiments showed that fruiting body was more effective to inhibit hepatocellular carcinoma cells than mycelia. High resolution electrospray ionization mass spectroscopy (HR-ESI-MS) analysis revealed fruiting body was rich in phenylpropanoids, and several unique phenylpropanoids in spp. exhibited potent anti-carcinogenesis activity. Based on genomic, HR-ESI-MS information and differentially expressed genes in transcriptome analysis, we deduced the biosynthesis pathway of four major phenylpropanoids in . Transcriptome analysis revealed the deduced genes expressions were synergistically changed with the production of phenylpropanoids. The optimal candidate genes of phenylpropanoids' synthesis pathway were screened by molecular docking analysis. Overall, our results provided a high-quality genomic data of and inferred biosynthesis pathways of four phenylpropanoids with potent anti-carcinogenesis activities. These will be a valuable resource for further genetic improvement and effective use of the .
(猪苓)猪苓是“桑黄”的一种,其多种药用价值已有充分记载,但基因组信息和活性成分在很大程度上尚不清楚。在此,我们对猪苓进行了全基因组测序,确定苯丙烷类化合物为其关键抗癌成分,并推导了它们的生物合成途径。组装了一个41.11 Mb的基因组序列,利用高通量染色体构象捕获技术数据创建的热图表明,所有片段可清晰地分为11条假染色体。细胞实验表明,猪苓子实体对肝癌细胞的抑制作用比菌丝体更有效。高分辨率电喷雾电离质谱(HR-ESI-MS)分析显示,猪苓子实体富含苯丙烷类化合物,猪苓属中的几种独特苯丙烷类化合物具有强大的抗癌活性。基于基因组、HR-ESI-MS信息以及转录组分析中的差异表达基因,我们推导了猪苓中四种主要苯丙烷类化合物的生物合成途径。转录组分析表明,推导的基因表达与苯丙烷类化合物的产生协同变化。通过分子对接分析筛选出苯丙烷类化合物合成途径的最佳候选基因。总体而言,我们的结果提供了高质量的猪苓基因组数据,并推断了四种具有强大抗癌活性的苯丙烷类化合物的生物合成途径。这些将成为猪苓进一步遗传改良和有效利用的宝贵资源。