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Agrobacterium and Viral Vectors-Mediated In vivo Gene Silencing Assays in Plants

机译:农杆菌和病毒载体介导的植物体内基因沉默测定

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Over the last years, the explosive growth of plant genomic resources and the development of advanced vectors enhanced the emergence of rapid systems to dissect plant gene function. Although transgenic approach has been applied to generate stable transgenic lines, this procedure is time-consuming and labor-intensive. Transient expression systems are continuously emerging during these years as an alternative tool for functional genomics studies in plants. Among these techniques, Agrobacterium -infiltration and infectious clones-derived plant viruses have been developed and successfully applied for versatile transient assays. Their effectiveness over a wide range of plant species is often validated. Here, the green fluorescent protein (GFP) gene was investigated as reporter gene for proof-of-concept to induce gene silencing in GFP-transgenic tobacco and grapevine plants either by inoculation of Arabis mosaic virus infectious clones or through in planta vacuum infiltration of Agrobacterium suspension.
机译:在过去的几年中,植物基因组资源的爆炸性增长和先进载体的发展促进了解剖植物基因功能的快速系统的出现。尽管已经使用转基因方法来产生稳定的转基因品系,但是该过程费时且费力。近年来,瞬态表达系统作为植物功能基因组学研究的替代工具不断涌现。在这些技术中,农杆菌浸润和传染性克隆衍生的植物病毒已被开发出来,并成功地用于各种瞬时分析。通常可以验证它们在多种植物物种中的有效性。在这里,绿色荧光蛋白(GFP)基因被研究为报告基因,用于概念证明,通过接种Arabis花叶病毒感染性克隆或通过农杆菌在植物中的真空浸润诱导GFP转基因烟草和葡萄植物中的基因沉默悬挂。

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