Wang Chengcheng, Chen Lihong, Cai Zhichen, Chen Cuihua, Liu Zixiu, Liu Shengjin, Zou Lisi, Tan Mengxia, Chen Jiali, Liu Xunhong, Mei Yuqi, Wei Lifang, Liang Juan, Chen Jine
School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing, China.
School of Pharmacy, Jiangsu Vocational College of Medicine, Yancheng, China.
Front Plant Sci. 2021 Oct 7;12:727882. doi: 10.3389/fpls.2021.727882. eCollection 2021.
Salinity stress significantly affects the contents of bioactive constituents in licorice . To elucidate the molecular mechanism underlying the difference in the accumulation of these constituents under sodium chloride (NaCl, salt) stress, licorice seedlings were treated with NaCl and then subjected to an integrated transcriptomic and metabolite profiling analysis. The transcriptomic analysis results identified 3,664 differentially expressed genes (DEGs) including transcription factor family MYB and basic helix-loop-helix (). Most DEGs were involved in flavonoid and terpenoid biosynthesis pathways. In addition, 121 compounds including a triterpenoid and five classes of flavonoids (isoflavone, flavone, flavanone, isoflavan, and chalcone) were identified, and their relative levels were compared between the stressed and control groups using data from the ultrafast liquid chromatography (UFLC)-triple quadrupole-time of flight-tandem mass spectrometry (TOF-MS/MS) analysis. Putative biosynthesis networks of the flavonoids and triterpenoids were created and combined with structural DEGs such as phenylalanine ammonia-lyase (), 4-coumarate-CoA ligase [], cinnamate 4-hydroxylase [], chalcone synthase [], chalcone-flavanone isomerase [], and flavonoid-3',5' hydroxylase ('') for flavonoids, and and for glycyrrhizin biosynthesis. Notably, significant upregulation of UDP-glycosyltransferase genes () in salt-stressed licorice indicated that postmodification of glycosyltransferase may participate in downstream biosynthesis of flavonoid glycosides and triterpenoid saponins. Accordingly, the expression trend of the DEGs is positively correlated with the accumulation of glycosides. Our study findings indicate that key DEGs and crucial genes co-regulate flavonoid and saponin biosynthesis in licorice under salt stress.
盐胁迫显著影响甘草中生物活性成分的含量。为了阐明在氯化钠(NaCl,盐)胁迫下这些成分积累差异的分子机制,对甘草幼苗进行NaCl处理,然后进行转录组和代谢物谱综合分析。转录组分析结果鉴定出3664个差异表达基因(DEG),包括转录因子家族MYB和碱性螺旋-环-螺旋(bHLH)。大多数DEG参与黄酮类和萜类生物合成途径。此外,鉴定出121种化合物,包括一种三萜类化合物和五类黄酮类化合物(异黄酮、黄酮、黄烷酮、异黄烷和查尔酮),并使用超快速液相色谱(UFLC)-三重四极杆-飞行时间串联质谱(TOF-MS/MS)分析数据比较了胁迫组和对照组之间它们的相对水平差异。构建了黄酮类和三萜类化合物的假定生物合成网络,并与黄酮类化合物的结构DEG如苯丙氨酸解氨酶(PAL)、4-香豆酸-CoA连接酶(4CL)、肉桂酸4-羟化酶(C4H)、查尔酮合酶(CHS)、查尔酮-黄烷酮异构酶(CHI)和黄酮-3',5'-羟化酶(F3'5'H),以及甘草酸生物合成的β-香树素合酶(β-AS)和鲨烯环氧酶(SE)相结合。值得注意的是,盐胁迫甘草中尿苷二磷酸糖基转移酶基因(UGT)的显著上调表明糖基转移酶的后修饰可能参与黄酮糖苷和三萜皂苷的下游生物合成。因此,DEG的表达趋势与糖苷的积累呈正相关。我们的研究结果表明,关键DEG和关键UGT基因共同调控盐胁迫下甘草中黄酮类和皂苷类的生物合成。