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含截短的农杆菌 virE2 的转基因葡萄砧木对冠瘿病的抗性。

Resistance to crown gall disease in transgenic grapevine rootstocks containing truncated virE2 of Agrobacterium.

机构信息

Department of Plant Pathology and Plant-Microbe Biology, Cornell University, New York State Agricultural Experiment Station, Geneva, NY 14456, USA.

出版信息

Transgenic Res. 2010 Dec;19(6):949-58. doi: 10.1007/s11248-010-9373-x. Epub 2010 Feb 25.

Abstract

A truncated form of the Ti-plasmid virE2 gene from Agrobacterium tumefaciens strains C58 and A6, and A. vitis strain CG450 was transferred and expressed in somatic embryos of grapevine rootstocks 110 Richter (Vitis rupestris × V. berlandieri), 3309 Couderc (V. rupestris × V. riparia) and Teleki 5C (V. berlandieri × V. riparia) via Agrobacterium-mediated transformation to confer resistance to crown gall disease. Transformation was confirmed in 98% of the 322 lines by enzyme-linked immunosorbent assay for the neomycin phosphotransferase II protein and 97% of 295 lines by polymerase chain reaction for the truncated virE2 transgene. Southern blot analysis revealed the insertion of truncated virE2 at one to three loci in a subset of seven transgenic 110 Richter lines. In vitro resistance screening assays based on inoculations of shoot internode sections showed reduced tumorigenicity and very small galls in 23 of 154 transgenic lines. Non-transformed controls had a 100% tumorigenicity rate with very large galls. Disease resistance assay at the whole plant level in the greenhouse revealed seven transgenic lines (3 lines of 110 Richter, 2 lines of 3309 Couderc and 2 lines of Teleki 5C) were resistant to A. tumefaciens strain C58 and A. vitis strains TM4 and CG450 with a substantially reduced percentage of inoculation sites showing gall as compared to controls. No association was found between the level of resistance to crown gall disease and the source Agrobacterium strain of virE2. Taken together, our data showed that resistance to crown gall disease can be achieved by expressing a truncated form of virE2 in grapevines.

摘要

根癌农杆菌 Ti 质粒 virE2 基因的截短形式,来自于农杆菌菌株 C58 和 A6,以及 A. vitis 菌株 CG450,通过根癌农杆菌介导的转化,转移并在葡萄砧木 110 里奇特(Vitis rupestris×V. berlandieri)、3309 库德尔(V. rupestris×V. riparia)和 Teleki 5C(V. berlandieri×V. riparia)的体细胞胚中表达,赋予其对冠瘿病的抗性。通过酶联免疫吸附试验(ELISA)检测新霉素磷酸转移酶 II 蛋白,在 322 个转化系中,有 98%得到了证实;通过聚合酶链反应(PCR)检测截短的 virE2 转基因,有 97%得到了证实。Southern blot 分析显示,在 7 个转基因 110 里奇特系的亚组中,virE2 截短基因被插入到一个到三个位点。基于接种茎节段的体外抗性筛选试验显示,在 154 个转基因系中的 23 个系中,肿瘤发生的程度降低,肿瘤很小。非转化对照系的肿瘤发生率为 100%,肿瘤很大。温室的整株水平的抗病性试验表明,有 7 个转基因系(110 里奇特的 3 个系、3309 库德尔的 2 个系和 Teleki 5C 的 2 个系)对根癌农杆菌菌株 C58 和 A. vitis 菌株 TM4 和 CG450 具有抗性,与对照相比,接种部位显示出肿瘤的比例显著降低。virE2 的抗性与根癌农杆菌菌株来源之间没有关联。总的来说,我们的数据表明,通过在葡萄中表达 virE2 的截短形式,可以实现对冠瘿病的抗性。

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