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Agrobacterium-mediated genetic transformation of yam (Dioscorea rotundata): an important tool for functional study of genes and crop improvement

机译:农杆菌介导的山药遗传转化:基因功能研究和作物改良的重要工具

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摘要

Although genetic transformation of clonally propagated crops has been widely studied as a tool for crop improvement and as a vital part of the development of functional genomics resources, there has been no report of any existing Agrobacterium-mediated transformation of yam (Dioscorea spp.) with evidence of stable integration of T-DNA. Yam is an important crop in the tropics and subtropics providing food security and income to over 300 million people. However, yam production remains constrained by increasing levels of field and storage pests and diseases. A major constraint to the development of biotechnological approaches for yam improvement has been the lack of an efficient and robust transformation and regeneration system. In this study, we developed an Agrobacterium-mediated transformation of Dioscorea rotundata using axillary buds as explants. Two cultivars of D. rotundata were transformed using Agrobacterium tumefaciens harboring the binary vectors containing selectable marker and reporter genes. After selection with appropriate concentrations of antibiotic, shoots were developed on shoot induction and elongation medium. The elongated antibiotic-resistant shoots were subsequently rooted on medium supplemented with selection agent. Successful transformation was confirmed by polymerase chain reaction, Southern blot analysis, and reporter genes assay. Expression of gusA gene in transgenic plants was also verified by reverse transcription polymerase chain reaction analysis. Transformation efficiency varied from 9.4 to 18.2% depending on the cultivars, selectable marker genes, and the Agrobacterium strain used for transformation. It took 3–4 months from Agro-infection to regeneration of complete transgenic plant. Here we report an efficient, fast and reproducible protocol for Agrobacterium-mediated transformation of D. rotundata using axillary buds as explants, which provides a useful platform for future genetic engineering studies in this economically important crop.
机译:尽管已经广泛研究了无性繁殖作物的遗传转化,作为改良作物的工具,并且是功能基因组学资源发展的重要组成部分,但尚无关于农杆菌介导的山药转化的任何报道(Dioscorea spp。)。 T-DNA稳定整合的证据。薯类是热带和亚热带的重要作物,可为3亿多人提供粮食安全和收入。但是,山药的生产仍然受到田间和储藏病虫害和疾病增加的限制。开发用于改良山药的生物技术方法的主要制约因素是缺乏有效而稳健的转化和再生系统。在这项研究中,我们使用腋芽作为外植体,开发了土壤杆菌介导的农杆菌介导的转化。使用携带含有选择标记和报道基因的二元载体的根癌农杆菌转化两个圆盘杜鹃的栽培种。用适当浓度的抗生素选择后,在芽诱导和伸长培养基上形成芽。随后将伸长的抗生素抗性芽生根于补充有选择剂的培养基上。通过聚合酶链反应,Southern印迹分析和报告基因分析证实成功转化。还通过逆转录聚合酶链反应分析证实了gusA基因在转基因植物中的表达。转化效率从9.4%到18.2%不等,具体取决于品种,选择标记基因和用于转化的农杆菌菌株。从农业感染到完整的转基因植物的再生花了3-4个月。在这里,我们报告了一种高效,快速且可重现的协议,用于使用腋芽作为外植体的土壤杆菌介导的农杆菌介导的转化,这为该经济重要作物的未来基因工程研究提供了有用的平台。

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