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首页> 外文期刊>Plant molecular biology reporter >Transgenic Potato Plants Expressing StoVe1 Exhibit Enhanced Resistance to Verticillium dahliae
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Transgenic Potato Plants Expressing StoVe1 Exhibit Enhanced Resistance to Verticillium dahliae

机译:表达StoVe1的转基因马铃薯植株对黄萎病菌的抗性增强

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摘要

Verticillium wilt is a persistent and serious disease in potato production mainly caused by soil-borne fungus Verticillium dahliae. In our previous experiment, StoVe1 gene was cloned from Solanum torvum, a wild relative of eggplant which was shown to be highly resistant to fungal wilts. In order to analyze the function of StoVe1 gene, the StoVe1 gene was sub-cloned into vector pCMBIA1304 and the recombination vector was introduced into the potato cultivar D,sir,e plants by Agrobacterium-mediated transformation. A total of 25 Hygromycin B-resistant plants were generated with ten independent transgenic lines identified by PCR and GUS staining analysis. The expression of StoVe1 gene in transgenic lines C9, C17, and C24 which were selected randomly was examined by quantitative RT-PCR. The resistance of transgenic lines to V. dahliae was also evaluated by in vitro antifungal and in vivo plant infection assays. The result showed that StoVe1 gene revealed its expression in all analyzed lines and the level of the transcript was 5.3- to 9.0-fold of that of the control. The antifungal assay revealed that transgenic lines C9, C17, and C24 had threefold higher than control plants and had higher inhibition rates of 45.5%, 44.5%, and 39.4% respectively. This result was confirmed by plant infection assay and the selected three lines were more resistant to V. dahliae infection, with disease index of 15 to 35, about one half to one fourth of that of the control and disease incidences of 20% to 50% and about one half to one fourth of that in control plants. It revealed that the overexpression of StoVe1 gene in transgenic potato lines enhanced plant resistance to V. dahliae.
机译:黄萎病是马铃薯生产中的一种持续严重的疾病,主要由土壤传播的真菌黄萎病引起。在我们之前的实验中,StoVe1基因是从茄子的野生近缘种茄子中克隆得到的,茄子对真菌青枯病具有高度抗性。为了分析StoVe1基因的功能,将StoVe1基因亚克隆到载体pCMBIA1304中,并通过农杆菌介导的转化将重组载体引入马铃薯D,sir,e植物中。通过PCR和GUS染色分析鉴定出总共25个潮霉素B抗性植物,其具有十个独立的转基因系。通过定量RT-PCR检查StoVe1基因在随机选择的转基因系C9,C17和C24中的表达。还通过体外抗真菌和体内植物感染测定法评估了转基因株系对大丽弧菌的抗性。结果表明,StoVe1基因在所有分析品系中均显示出其表达,其转录水平是对照的5.3-9.0倍。抗真菌试验表明,转基因品系C9,C17和C24比对照植物高三倍,抑制率分别为45.5%,44.5%和39.4%。该结果通过植物感染测定法得到证实,所选的三株品系对大丽弧菌的感染更具抗性,疾病指数为15至35,约为对照的一半至四分之一,疾病发生率为20%至50%大约是对照植物的一半到四分之一。这表明在转基因马铃薯品系中StoVe1基因的过表达增强了植物对大丽花的抗性。

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