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通过农杆菌浸润和发根转化联合筛选系统鉴定参与异黄酮生物合成途径的新型MYB转录因子。

Identification of novel MYB transcription factors involved in the isoflavone biosynthetic pathway by using the combination screening system with agroinfiltration and hairy root transformation.

作者信息

Sarkar Md Abdur Rauf, Watanabe Satoshi, Suzuki Akihiro, Hashimoto Fumio, Anai Toyoaki

机构信息

The United Graduate School of Agricultural Sciences, Kagoshima University, 1-21-24 Korimoto, Kagoshima 890-0065, Japan.

Faculty of Agriculture, Saga University, 1 Honjo-machi, Saga 840-8502, Japan.

出版信息

Plant Biotechnol (Tokyo). 2019 Dec 25;36(4):241-251. doi: 10.5511/plantbiotechnology.19.1025a.

Abstract

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 and the isoflavone synthase (IFS) genes and in the isoflavone biosynthetic pathway. In the agroinfiltration assay, we co-transformed a ( gene) promoter-fused gene with target promoter-fused (β-glucuronidase) gene constructs, and identified three genes (, , and ) 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 MYB-overexpressing 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 , , and 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.

摘要

大豆异黄酮是功能上重要的次生代谢产物,主要积累在种子中。它们的生物合成过程在转录水平上受到协调调控;然而,关键转录因子(TFs)的筛选系统有限。在这里,我们开发了一种组合筛选系统,该系统包括一个简单的农杆菌浸润试验和一个强大的毛状根转化试验。首先,我们筛选了可以激活异黄酮生物合成途径中查尔酮合酶(CHS)基因以及异黄酮合酶(IFS)基因 和 的启动子的候选MYB转录因子。在农杆菌浸润试验中,我们将一个 ( 基因)启动子融合的 基因与靶启动子融合的 (β-葡萄糖醛酸酶)基因构建体共转化,并鉴定出三个基因( 、 和 )作为异黄酮生物合成的候选调节因子。然后,我们利用大豆毛状根转化试验评估了鉴定出的三个MYB基因在异黄酮生物合成中对异黄酮积累的功能调节作用。三个候选MYB基因在毛状根转基因系中显示出总异黄酮积累增加。三个MYB过表达系中总异黄酮的积累比载体对照大约多2至4倍,证实了它们在调节异黄酮生物合成中的可能作用。然而,除了GmMYB502过表达系外,未观察到真实的 、 和 转录本的显著积累。因此,转基因毛状根中异黄酮积累的分析对于评估MYB转录因子对异黄酮生物合成基因的反式激活活性是有效的。我们的结果证明了一个简单而强大的系统,该系统有可能鉴定不同植物代谢途径中孤儿转录因子的功能。

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