Lin Tingwen, Du Jinfa, Zheng Xiaoyan, Zhou Ping, Li Ping, Lu Xu
State Key Laboratory of Natural Medicines, School of Traditional Chinese Pharmacy, China Pharmaceutical University, 24 Tongjia Lane, Nanjing, 210009 People's Republic of China.
3 Biotech. 2020 Jul;10(7):290. doi: 10.1007/s13205-020-02246-w. Epub 2020 Jun 5.
Differential transcriptome analysis is an effective method for gene selection of triterpene saponin biosynthetic pathways. MeJA-induced differential transcriptome of has not been analyzed yet. In this study, comparative transcriptome analysis of roots and methyl jasmonate (MeJA)-induced roots revealed 83,532 assembled unigenes and 21,947 differentially expressed unigenes. Sixteen AP2/ERF transcription factors, which were significantly induced by MeJA treatment in the root of , were selected for further analysis. Real-time quantitative PCR (RT-qPCR) and co-expression network analysis of the 16 AP2/ERF transcription factors showed that and had significant correlation with dammarenediol II synthase gene () and squalene epoxidase gene (), which are key genes in notoginsenoside biosynthesis, in different tissues and MeJA-induced roots. A phylogenetic tree was conducted to analyze the 16 candidate AP2/ERF transcription factors and other 38 transcription factors. The phylogenetic tree analysis showed PnERF2, AtERF3, AtERF7, TcERF12 and other seven transcriptional factors are in same branch, while PnERF3 had close evolutionary relationships with AtDREB1A, GhERF38 and TcAP2. The results of comparative transcriptomes and AP2/ERF transcriptional factors analysis laid a solid foundation for further investigations of disease resistance and notoginsenoside biosynthesis in .
差异转录组分析是三萜皂苷生物合成途径基因筛选的有效方法。茉莉酸甲酯(MeJA)诱导的[植物名称未给出]差异转录组尚未进行分析。在本研究中,对[植物名称未给出]根和茉莉酸甲酯(MeJA)诱导的根进行比较转录组分析,共鉴定出83,532个组装单基因和21,947个差异表达单基因。选择了16个在[植物名称未给出]根中受MeJA处理显著诱导的AP2/ERF转录因子进行进一步分析。对这16个AP2/ERF转录因子的实时定量PCR(RT-qPCR)和共表达网络分析表明,在不同组织和MeJA诱导的根中,[基因名称未给出]和[基因名称未给出]与三七皂苷生物合成的关键基因达玛烯二醇-II合成酶基因([基因名称未给出])和鲨烯环氧酶基因([基因名称未给出])具有显著相关性。构建了系统发育树来分析这16个候选AP2/ERF转录因子和其他38个转录因子。系统发育树分析表明,PnERF2、AtERF3、AtERF7、TcERF12和其他七个转录因子位于同一分支,而PnERF3与AtDREB1A、GhERF38和TcAP2具有密切的进化关系。比较转录组和AP2/ERF转录因子分析结果为进一步研究[植物名称未给出]的抗病性和三七皂苷生物合成奠定了坚实基础。