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首页> 外文期刊>Molecular Plant >pHairyRed: A Novel Binary Vector Containing the DsRed2 Reporter Gene for Visual Selection of Transgenic Hairy Roots
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pHairyRed: A Novel Binary Vector Containing the DsRed2 Reporter Gene for Visual Selection of Transgenic Hairy Roots

机译:pHairyRed:一种新颖的二进制载体,包含用于可视化选择转基因毛根的DsRed2报告基因

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We developed a new plant transformation vector, pHairyRed, for enabling high throughput, non-destructive selection of Agrobacterium rhizogenes-mediated ‘hairy-root’ transformation. pHairyRed allows easy in planta visualization of transgenic tissue with minimal disturbance to the plant. The DsRed2 reporter gene, encoding a red fluorescent protein, was cloned to yield pHairyRed (harbouring a multiple cloning site), which was used with the highly efficient K599 A. rhizogenes strain to infect soybean (Glycine max L. Merrill) plants. DsRed2 fluorescence was easily detected in planta for the duration of a 5-week study with negligible levels of background autofluorescence. This enabled visual selection of transformed roots and subsequent excission of non-transformed roots. pHairyRed-transformed roots nodulated normally when inoculated with Bradyrhizobium japonicum. Within the nodule, DsRed2 fluorescence was plant-specific, being absent in the bacteroid-dominated nodule infected zone. To test the reliability of pHairyRed as a high-fidelity binary vector reporter system, the gene encoding the soybean Nod factor receptor, GmNFR1α, was cloned into the vector for use in a complementation study with a non-nodulating nfr1α mutant of soybean. Complementation was achieved and, without exception, DsRed2 fluorescence was detected in all hairy roots that successfully formed nodules (100%, n = 34). We anticipate broad application of this reporter system for the further analysis of root-related events in soybean and related legumes.
机译:我们开发了一种新的植物转化载体pHairyRed,可用于高通量,无损选择发根农杆菌介导的“毛根”转化。 pHairyRed可以在植物中轻松显示转基因组织,而对植物的干扰最小。克隆编码红色荧光蛋白的DsRed2报告基因产生pHairyRed(具有多个克隆位点),将其与高效K599发根农杆菌菌株一起感染大豆(Glycine max L. Merrill)植物。在为期5周的研究中,很容易在植物中检测到DsRed2荧光,而背景自发荧光水平可忽略不计。这样就可以目视选择转化根和随后去除未转化根。 pHairy接种日本慢生根瘤菌后,红色转化的根通常呈根瘤状。在结核内,DsRed2荧光是植物特有的,在以细菌为主导的结核感染区中不存在。为了测试pHairyRed作为高保真二元载体报告系统的可靠性,将编码大豆Nod因子受体GmNFR1α的基因克隆到载体中,用于与大豆的非结瘤nfr1α突变体进行互补研究。实现了互补,并且毫无例外地,在所有成功形成根瘤的毛状根中均检测到DsRed2荧光(100%,n = 34)。我们预期该报告系统的广泛应用将进一步分析大豆和相关豆类中与根相关的事件。

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