Liu Houbo, Huang Ceyin, Li Qingqing, Wang Mufei, Xiao Shiji, Shi Junhua, He Yihuai, Wen Weie, Li Lin, Xu Delin
Department of Cell Biology, Zunyi Medical University, Zunyi, China.
Department of Dermatology, Chengdu Second People's Hospital, Chengdu, China.
Front Plant Sci. 2022 Jun 17;13:875404. doi: 10.3389/fpls.2022.875404. eCollection 2022.
To screen the genes regulating the biosynthesis of phenolic acid derivatives from the genome of , we designed a suspension culture system to sample the cells for the following experiments. The contents of four phenolic acid derivatives were determined by high-performance liquid chromatography, and several full-length transcriptome sequencings of RNA samples at 10 time points were performed for bioinformatics analysis. The correlation analysis was used to identify and verify the key DEGs involved in the biosynthesis of the four phenolic acid derivatives. The results showed that the contents of p-hydroxybenzylalcohol (HBA), Dactylorhin A, Militarine, and Coelonin peaked at 33 days postinoculation (Dpi), 18 Dpi, 39 Dpi, and 39 Dpi of the culture system, respectively. Based on transcriptome data, 80 DEGs involved in the biosynthesis of phenolic acid derivatives were obtained. The KEGG pathway enrichment analysis classified them mostly into five metabolic pathways: phenylpropane biosynthesis, starch and sucrose metabolic, cyanoamino acid metabolism, gluconeogenesis and glycolysis, and phenylalanine metabolism. qPCR analysis revealed that the relative gene expression levels were consistent with the overall trend of transcriptome sequencing results. Among them, 14, 18, 23, and 41 unigenes were found to be involved in the synthesis of HBA, Dactylorhin A, Coelonin, and Militarine, respectively. These unigenes laid a solid foundation for elucidating the biosynthesis mechanism of phenolic acid derivatives in suspension cells of .
为了从[具体物种]的基因组中筛选调控酚酸衍生物生物合成的基因,我们设计了一种悬浮培养系统来采集细胞用于后续实验。通过高效液相色谱法测定了四种酚酸衍生物的含量,并对RNA样本在10个时间点进行了多次全长转录组测序以进行生物信息学分析。采用相关性分析来鉴定和验证参与四种酚酸衍生物生物合成的关键差异表达基因(DEGs)。结果表明,对羟基苯甲醇(HBA)、毛兰素A、毛兰素和蛇舌兰素的含量分别在培养系统接种后33天(Dpi)、18 Dpi、39 Dpi和39 Dpi达到峰值。基于转录组数据,获得了80个参与酚酸衍生物生物合成的DEGs。KEGG通路富集分析将它们主要分为五个代谢途径:苯丙烷生物合成、淀粉和蔗糖代谢、氰基氨基酸代谢、糖异生和糖酵解以及苯丙氨酸代谢。qPCR分析表明,相对基因表达水平与转录组测序结果的总体趋势一致。其中,分别发现有14、18、23和41个单基因参与HBA、毛兰素A、蛇舌兰素和毛兰素的合成。这些单基因为阐明[具体物种]悬浮细胞中酚酸衍生物的生物合成机制奠定了坚实基础。