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Functional Characterization of a Novel R2R3-MYB Transcription Factor Modulating the Flavonoid Biosynthetic Pathway from Epimedium sagittatum

机译:新型R2R3-MYB转录因子调节 italic> Epimedium sagittatum 黄酮生物合成途径的功能表征

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Epimedium species have been widely used both as traditional Chinese medicinal plants and ornamental perennials. Both flavonols, acting as the major bioactive components (BCs) and anthocyanins, predominantly contributing to the color diversity of Epimedium flowers belong to different classes of flavonoids. It is well-acknowledged that flavonoid biosynthetic pathway is predominantly regulated by R2R3-MYB transcription factor (TF) as well as bHLH TF and WD40 protein at the transcriptional level. MYB TFs specifically regulating anthocyanin or flavonol biosynthetic pathway have been already isolated and functionally characterized from Epimedium sagittatum , but a R2R3-MYB TF involved in regulating both these two pathways has not been functionally characterized to date in Epimedium plants. In this study, we report the functional characterization of EsMYB9 , a R2R3-MYB TF previously isolated from E. sagittatum . The previous study indicated that EsMYB9 belongs to a small subfamily of R2R3-MYB TFs containing grape VvMYB5a and VvMYB5b TFs, which regulate flavonoid biosynthetic pathway. The present studies show that overexpression of EsMYB9 in tobacco leads to increased transcript levels of flavonoid pathway genes and increased contents of anthocyanins and flavonols. Yeast two-hybrid assay indicates that the C-terminal region of EsMYB9 contributes to the autoactivation activity, and EsMYB9 interacts with EsTT8 or AtTT8 bHLH regulator. Transient reporter assay shows that EsMYB9 slightly activates the expression of EsCHS (chalcone synthase) promoter in transiently transformed leaves of Nicotiana benthamiana , but the addition of AtTT8 or EsTT8 bHLH regulator strongly enhances the transcriptional activation of EsMYB9 against five promoters of the flavonoid pathway genes except EsFLS (flavonol synthase). In addition, co-transformation of EsMYB9 and EsTT8 in transiently transfected tobacco leaves strongly induces the expressions of flavonoid biosynthetic genes. The potential role of EsMYB9 in modulating the biosynthesis and accumulation of sucrose-induced anthocyanin and flavonol-derived BCs is also discussed. These findings suggest that EsMYB9 is a novel R2R3-MYB TF, which regulates the flavonoid biosynthetic pathway in Epimedium , but distinctly different with the anthocyanin or flavonol-specific MYB regulators identified previously in Epimedium plants.
机译:淫羊species已被广泛用作中药材和多年生观赏植物。充当主要生物活性成分(BCs)的黄酮醇和主要促进淫羊med花颜色多样性的花色苷都属于不同类别的黄酮类。众所周知,类黄酮的生物合成途径主要受R2R3-MYB转录因子(TF)以及bHLH TF和WD40蛋白在转录水平上的调控。已经从淫羊Epi淫羊med中分离出了专门调节花色苷或黄酮醇生物合成途径的MYB TF,并对其功能进行了表征,但是迄今为止,在淫羊plants植物中尚未对参与调节这两个途径的R2R3-MYB TF进行功能表征。在这项研究中,我们报告了EsMYB9的功能特性,EsMYB9是先前从箭叶分离出的R2R3-MYB TF。先前的研究表明,EsMYB9属于R2R3-MYB TF的一个小亚家族,其中包含调节类黄酮生物合成途径的葡萄VvMYB5a和VvMYB5b TF。目前的研究表明,烟草中EsMYB9的过表达导致类黄酮途径基因的转录水平升高,以及花青素和黄酮醇含量增加。酵母两杂交试验表明EsMYB9的C末端区域有助于自激活活性,并且EsMYB9与EsTT8或AtTT8 bHLH调节剂相互作用。瞬时报告基因分析表明,EsMYB9稍微激活了烟草瞬时转化叶片中EsCHS(查尔酮合酶)启动子的表达,但添加AtTT8或EsTT8 bHLH调节剂可强烈增强EsMYB9对除类黄酮途径基因的五个启动子的转录激活EsFLS(黄酮醇合酶)。另外,在瞬时转染的烟叶中EsMYB9和EsTT8的共转化强烈诱导了类黄酮生物合成基因的表达。还讨论了EsMYB9在调节蔗糖诱导的花色苷和黄酮醇衍生的BCs的生物合成和积累中的潜在作用。这些发现表明,EsMYB9是一种新型的R2R3-MYB TF,它调节淫羊med中的类黄酮生物合成途径,但与先前在淫羊ium植物中鉴定的花色苷或黄酮特定的MYB调节剂明显不同。

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