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Agrobacterium tumefaciens-mediated transformation of poinsettia, Euphorbia pulcherrima, with virus-derived hairpin RNA constructs confers resistance to Poinsettia mosaic virus

机译:农杆菌介导的一品红,大戟一品红与病毒衍生的发夹RNA构建体赋予对一品红花叶病毒的抗性

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摘要

Agrobacterium-mediated transformation for poinsettia (Euphorbia pulcherrima Willd. Ex Klotzsch) is reported here for the first time. Internode stem explants of poinsettia cv. Millenium were transformed by Agrobacterium tumefaciens, strain LBA 4404, harbouring virus-derived hairpin (hp) RNA gene constructs to induce RNA silencing-mediated resistance to Poinsettia mosaic virus (PnMV). Prior to transformation, an efficient somatic embryogenesis system was developed for poinsettia cv. Millenium in which about 75% of the explants produced somatic embryos. In 5 experiments utilizing 868 explants, 18 independent transgenic lines were generated. An average transformation frequency of 2.1% (range 1.2–3.5%) was revealed. Stable integration of transgenes into the poinsettia nuclear genome was confirmed by PCR and Southern blot analysis. Both single- and multiple-copy transgene integration into the poinsettia genome were found among transformants. Transgenic poinsettia plants showing resistance to mechanical inoculation of PnMV were detected by double antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA). Northern blot analysis of low molecular weight RNA revealed that transgene-derived small interfering (si) RNA molecules were detected among the poinsettia transformants prior to inoculation. The Agrobacterium-mediated transformation methodology developed in the current study should facilitate improvement of this ornamental plant with enhanced disease resistance, quality improvement and desirable colour alteration. Because poinsettia is a non-food, non-feed plant and is not propagated through sexual reproduction, this is likely to be more acceptable even in areas where genetically modified crops are currently not cultivated.
机译:首次报道了农杆菌介导的一品红(大戟(Euphorbia pulcherrima Willd。Ex Klotzsch))的转化。一品红的节间茎外植体。千株被根癌农杆菌LBA 4404株转化,它携带病毒衍生的发夹(hp)RNA基因构建体,以诱导RNA沉默介导的对一品红花叶病毒(PnMV)的抗性。在转化之前,为一品红简历开发了有效的体细胞胚发生系统。千年,其中约75%的外植体产生体细胞胚。在利用868外植体的5个实验中,产生了18个独立的转基因品系。揭示出平均转换频率为2.1%(范围为1.2-3.5%)。通过PCR和Southern印迹分析证实了转基因稳定地整合到一品红核基因组中。在转化体中发现单拷贝和多拷贝转基因整合到一品红基因组中。通过双抗体夹心酶联免疫吸附测定(DAS-ELISA)检测显示出对PnMV的机械接种具有抗性的转基因一品红植物。低分子量RNA的Northern印迹分析表明,接种前在一品红转化子中检测到了转基因来源的小干扰(si)RNA分子。在当前研究中开发的农杆菌介导的转化方法应通过提高抗病性,质量改善和理想的颜色变化促进这种观赏植物的改良。由于一品红是非食用非饲料植物,不会通过有性繁殖繁殖,因此即使在目前未种植转基因作物的地区,一品红也可能被接受。

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