首页> 外文期刊>Plant Growth Regulation: An International Journal on Natural and Synthetic Regulators >Identification of biosynthetic pathways involved in flavonoid production in licorice by RNA-seq based transcriptome analysis
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Identification of biosynthetic pathways involved in flavonoid production in licorice by RNA-seq based transcriptome analysis

机译:基于RNA-SEQ的转录组分析鉴定甘草中的类黄酮产生的生物合成途径

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摘要

Liquiritin, a flavonoid, is a key medicinal ingredient in licorice (Glycyrrhiza uralensis), a commonly used herb in traditional Chinese medicine. Biosynthesis of flavonoids is a complex process that involves not only the phenylpropanoid biosynthetic pathway but also many other secondary metabolic pathways. In this study, we tried to identify the key enzymes and pathways for the biosynthesis of flavonoids in G. uralensis by analyzing the gene expression patterns in samples containing different levels of flavonoid. G. uralensis seeds were mutagenized by X-ray irradiation and samples were selected based on HPLC analysis. RNA-seq was used to examine the gene expression in two samples with high flavonoid content (H1 and H2) and one control sample (L1) with low flavonoid content. 61.37 million, 54.21 million, and 54.22 million clean reads were obtained in sample H1, H2, and L1, respectively. A total of 1875 core differentially expressed genes (DEGs) were identified. The expression patterns of core DEGs were similar in samples H1 and H2 but not in sample L1. Flavonoid metabolic pathway, terpenoid biosynthetic pathway, plant hormone signal transduction pathway, plant circadian rhythm pathway, and starch and sucrose metabolic pathway were found to play significant roles for flavonoid biosynthesis in licorice. Ten co-expressed DEGs on the five metabolic pathways were further verified by qRT-PCR, which confirmed that the RNA-Seq results were accurate and reliable. This study provides a basis for future functional genes mining and molecular regulatory mechanism elucidation of flavonoid biosynthesis in licorice.
机译:Lialiritin,一种类黄酮,是甘草(Glycyrrhiza Uralensis)的关键药物成分,中药常用的草药。黄酮类化合物的生物合成是一种复杂的方法,不仅涉及苯丙醇化生物合成途径,而且涉及许多其他次级代谢途径。在这项研究中,我们试图通过分析含有不同水平的样品中的样品中的基因表达模式来鉴定G. Uralensis中黄酮类化合物的生物合成的关键酶和途径。 G. uralensis种子通过X射线照射和样品基于HPLC分析来诱变。 RNA-SEQ用于检查具有高黄酮含量(H1和H2)的两种样品中的基因表达,以及具有低黄酮含量的一种对照样品(L1)。在样品H1,H2和L1中分别获得61.37百万,5421百万和54220万清洁读数。共鉴定了总共1875个核心差异表达基因(DEGS)。样品H1和H 2中的核心Degs的表达模式在样品L1中类似。意外表明类黄酮代谢途径,萜类生物合成途径,植物激素信号转导途径,植物昼夜节律途径和淀粉和蔗糖代谢途径在甘草中对黄酮类化合物进行显着作用。通过QRT-PCR进一步验证了在五种代谢途径上进行的十个共表达的DEG,这证实了RNA-SEQ结果准确可靠。本研究为未来的功能基因挖掘和分子调节机制阐明了甘草甘露治生物合成的基础。

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