首页> 外文期刊>BMC Genomics >De novo transcriptome sequencing and digital gene expression analysis predict biosynthetic pathway of rhynchophylline and isorhynchophylline from Uncaria rhynchophylla, a non-model plant with potent anti-alzheimer’s properties
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De novo transcriptome sequencing and digital gene expression analysis predict biosynthetic pathway of rhynchophylline and isorhynchophylline from Uncaria rhynchophylla, a non-model plant with potent anti-alzheimer’s properties

机译:从头转录组测序和数字基因表达分析预测了钩藤(Uncaria rhynchophylla)(一种具有强力抗阿尔茨海默氏性质的非典范植物)中的菱形茶碱和异喹啉碱的生物合成途径

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Background The major medicinal alkaloids isolated from Uncaria rhynchophylla (gouteng in chinese) capsules are rhynchophylline (RIN) and isorhynchophylline (IRN). Extracts containing these terpene indole alkaloids (TIAs) can inhibit the formation and destabilize preformed fibrils of amyloid β protein (a pathological marker of Alzheimer’s disease), and have been shown to improve the cognitive function of mice with Alzheimer-like symptoms. The biosynthetic pathways of RIN and IRN are largely unknown. Results In this study, RNA-sequencing of pooled Uncaria capsules RNA samples taken at three developmental stages that accumulate different amount of RIN and IRN was performed. More than 50 million high-quality reads from a cDNA library were generated and de novo assembled. Sequences for all of the known enzymes involved in TIAs synthesis were identified. Additionally, 193 cytochrome P450 (CYP450), 280 methyltransferase and 144 isomerase genes were identified, that are potential candidates for enzymes involved in RIN and IRN synthesis. Digital gene expression profile (DGE) analysis was performed on the three capsule developmental stages, and based on genes possessing expression profiles consistent with RIN and IRN levels; four CYP450s, three methyltransferases and three isomerases were identified as the candidates most likely to be involved in the later steps of RIN and IRN biosynthesis. Conclusion A combination of de novo transcriptome assembly and DGE analysis was shown to be a powerful method for identifying genes encoding enzymes potentially involved in the biosynthesis of important secondary metabolites in a non-model plant. The transcriptome data from this study provides an important resource for understanding the formation of major bioactive constituents in the capsule extract from Uncaria, and provides information that may aid in metabolic engineering to increase yields of these important alkaloids.
机译:背景技术从钩藤钩藤胶囊中分离出的主要药用生物碱是钩藤茶碱(RIN)和异叶钩藤茶碱(IRN)。含有这些萜烯吲哚生物碱(TIA)的提取物可以抑制淀粉样β蛋白(阿尔茨海默氏病的病理学标志物)的形成并破坏预形成的原纤维,并已显示出可以改善患有阿尔茨海默氏样症状的小鼠的认知功能。 RIN和IRN的生物合成途径在很大程度上是未知的。结果在这项研究中,对合并的Uncaria胶囊进行RNA测序,在三个发育阶段采集的RNA样品积累了不同量的RIN和IRN。从cDNA文库生成了超过5000万条高质量读物,并从头开始组装。确定了参与TIA合成的所有已知酶的序列。此外,还鉴定出193种细胞色素P450(CYP450),280种甲基转移酶和144种异构酶基因,它们是与RIN和IRN合成有关的酶的潜在候选者。在三个胶囊发育阶段,基于具有与RIN和IRN水平一致的表达谱的基因,进行了数字基因表达谱(DGE)分析。四个CYP450,三个甲基转移酶和三个异构酶被确定为最有可能参与RIN和IRN生物合成后续步骤的候选物。结论从头转录组组装和DGE分析相结合,是鉴定非模型植物中潜在编码重要次生代谢产物生物合成酶的基因的有效方法。这项研究的转录组数据为了解钩藤胶囊提取物中主要生物活性成分的形成提供了重要资源,并提供了有助于代谢工程提高这些重要生物碱产量的信息。

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