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首页> 外文期刊>Plant Biotechnology >Identification of novel MYB transcription factors involved in the isoflavone biosynthetic pathway by using the combination screening system with agroinfiltration and hairy root transformation
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Identification of novel MYB transcription factors involved in the isoflavone biosynthetic pathway by using the combination screening system with agroinfiltration and hairy root transformation

机译:通过使用具有农药和毛发根转化的组合筛选系统,鉴定涉及异黄酮生物合成途径的新型MYB转录因子

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Soybean isoflavones are functionally important secondary metabolites that are mainly accumulated in seeds. Their biosynthetic processes are regulated coordinately at the transcriptional level; however, screening systems for key transcription factors (TFs) are limited. Here we developed a combination screening system comprising a simple agroinfiltration assay and a robust hairy root transformation assay. First, we screened for candidate MYB TFs that could activate the promoters of the chalcone synthase (CHS) gene GmCHS8 and the isoflavone synthase (IFS) genes GmIFS1 and GmIFS2 in the isoflavone biosynthetic pathway. In the agroinfiltration assay, we co transformed a LjUbi (Lotus japonicus polyubiquitin gene) promoter-fused MYB gene with target promoter-fused GUS (beta-glucuronidase) gene constructs, and identified three genes (GmMYB102, GmMYB280, and GmMYB502) as candidate regulators of isoflavone biosynthesis. We then evaluated the functional regulatory role of identified three MYB genes in isoflavone biosynthesis using hairy roots transformation assay in soybean for the accumulation of isoflavones. Three candidate MYB genes showed an increased accumulation of total isoflavones in hairy root transgenic lines. Accumulation of total isoflavones in the three MYBoverexpressing lines was approximately 2 to 4-folds more than that in the vector control, confirming their possible role to regulate isoflavone biosynthesis. However, the significant accumulation of authentic GmCHS8, GmIFS1, and GmIFS2 transcripts could not be observed except for the GmMYB502-overexpressing line. Therefore, the analysis of isoflavone accumulation in transgenic hairy root was effective for evaluation of transactivation activity of MYB TFs for isoflavone biosynthetic genes. Our results demonstrate a simple and robust system that can potentially identify the function of orphan TFs in diverse plant metabolic pathways.
机译:大豆异黄酮是功能性重要的次生代谢产物,主要积累种子。它们的生物合成过程在转录水平方面进行调节;然而,用于关键转录因子(TFS)的筛选系统是有限的。在这里,我们开发了一种组合筛选系统,包括简单的农药滤波测定和鲁棒的毛状根转化测定。首先,我们筛选候选MYB TFS,其可以在异黄酮生物合成途径中激活Chalcode合酶(CHS)基因GMCHS8的启动子和异黄酮合酶(IFS)GMIFS1和GMIFS2。在农药融合的测定中,将Ljubi(莲花japonicus多泛素基因)启动子融合Myb基因转化为靶促进剂稠合的GUS(β-葡糖醛酸酶)基因构建体,并确定了三种基因(GMMyB102,GmmyB280和GmmyB502)作为候选调节剂异黄酮生物合成。然后,在大豆中使用毛状根转化测定来评估Isoflavone生物合成中鉴定的三种MYB基因的功能调节作用,用于在大豆中进行异黄酮的积累。三个候选MYB基因显示毛状根转基因系中总异黄酮的积累增加。三种MyboverCressizing系中总异黄酮的积累比载体对照中的三倍约为2至4倍,证实了调节异黄酮生物合成的可能作用。然而,除了GMMYB502过表达线外,无法观察到正品GMCHS8,GMIFS1和GMIFS2转录物的显着积累。因此,转基因毛状根中异黄酮积聚的分析对于评估异黄酮生物合成基因的MYB TFS的转基因活性是有效的。我们的结果表明了一种简单且稳健的系统,可以识别孤儿TFS在不同植物代谢途径中的功能。

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