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通过抑制原花青素基因 ANR1 和 ANR2 对转基因大豆进行花青素着色。

Coloring genetically modified soybean grains with anthocyanins by suppression of the proanthocyanidin genes ANR1 and ANR2.

机构信息

Bioproducts and Bioprocesses, Research Branch, Agriculture and Agri-Food Canada, Ottawa, ON, Canada.

出版信息

Transgenic Res. 2012 Aug;21(4):757-71. doi: 10.1007/s11248-011-9566-y. Epub 2011 Nov 15.

DOI:10.1007/s11248-011-9566-y
PMID:22083247
Abstract

Detection and quantification of the levels of adventitious presence of genetically modified (GM) soybeans in non-GM grain shipments currently requires sophisticated tests that can have issues with their reproducibility. We show here that pigment biosynthesis in the soybean seed coat can be manipulated to provide a distinct color that would enable the simple visible detection of the GM soybean grain. We observed that a distinct red-brown grain color could be engineered by the simultaneous suppression of two proanthocyanidin (PA) genes, ANTHOCYANIDIN REDUCTASE1 (ANR1) and ANR2. Multiple reaction monitoring by liquid chromatography tandem mass spectrometry was used to quantify differentially accumulated seed coat metabolites, and revealed the redirection of metabolic flux into the anthocyanin pigment pathway and unexpectedly the flavonol-3-O-glucoside pathway. The upregulations of anthocyanin isogenes (DFR1 and GST26) and the anthocyanin/flavonol-3-O-glycosyltransferase (UGT78K2) were identified by quantitative RT-PCR to be endogenous feedback and feedforward responses to overaccumulation of upstream flavonoid intermediates resulting from ANR1 and ANR2 suppressions. These results suggested the transcription of flavonoid genes to be a key component of the mechanism responsible for the redirection of metabolite flux. This report identifies the suppression of PA genes to be a novel approach for engineering pigmentation in soybean grains.

摘要

检测和定量非转基因谷物运输中存在的转基因(GM)大豆的水平目前需要复杂的测试,这些测试可能存在重复性问题。我们在这里展示,大豆种皮中的色素生物合成可以被操纵,以提供一种独特的颜色,从而能够简单地肉眼检测到转基因大豆颗粒。我们观察到,通过同时抑制两个原花青素(PA)基因,即花色素还原酶 1(ANR1)和 ANR2,可以产生明显的红棕色颗粒颜色。通过液相色谱串联质谱的多重反应监测来定量分析差异积累的种皮代谢物,并揭示了代谢通量向花青素色素途径和出人意料的类黄酮-3-O-葡萄糖苷途径的重新定向。通过定量 RT-PCR 鉴定出花青素异源基因(DFR1 和 GST26)和花青素/类黄酮-3-O-糖基转移酶(UGT78K2)的上调,是由于 ANR1 和 ANR2 抑制导致上游类黄酮中间产物过度积累而产生的内源反馈和前馈反应。这些结果表明,类黄酮基因的转录是导致代谢物通量重新定向的机制的关键组成部分。本报告确定了抑制 PA 基因是在大豆颗粒中进行色素工程的一种新方法。

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