首页> 外文期刊>Archives of virology >Transgenic resistance in potato plants expressing potato leaf roll virus (PLRV) replicase gene sequences is RNA-mediated and suggests the involvement of post-transcriptional gene silencing.
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Transgenic resistance in potato plants expressing potato leaf roll virus (PLRV) replicase gene sequences is RNA-mediated and suggests the involvement of post-transcriptional gene silencing.

机译:表达马铃薯叶卷病毒(PLRV)复制酶基因序列的马铃薯植株中的转基因抗性是RNA介导的,表明转录后基因沉默的参与。

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摘要

Genetically engineered expression of replicase encoding sequences has been proposed as an efficient system to confer protection against virus diseases by eliciting protection mechanisms in the plant. Potato leaf-roll was one of the first diseases for which this kind of protection was engineered in potato plants. However, details of the protecting mechanism were not reported, so far. The ORF2b of an Argentinean strain of PLRV was cloned and sequenced finding 94% and 97% of homology with Australian and Dutch strains, respectively. To elucidate the mechanism of protection against PLRV infection, three versions of ORF2b (non-translatable sense, translatable sense with an engineered ATG and antisense) were constructed under the control of the 35S CaMV promoter and the nos terminator and introduced in potato plants (cv. Kennebec) by Agrobacterium tumefaciens-mediated transformation. Grafting infection experiments showed that resistant transgenic plants could be obtained with any of the constructs, suggesting that the mechanism of protection is independent of the expression of protein and is RNA mediated. Field trial infection confirmed that resistant transgenic events were obtained. Biolistic transient transformation experiments of leaves derived from transgenic plants using a gene coding for the fusion protein GUS-ORF2b, followed by scoring of the number of GUS expressing leaf spots, supported that the protection is mediated by a post-transcriptional gene silencing mechanism.
机译:已经提出了基因工程改造的复制酶编码序列的表达,作为通过激发植物中的保护机制而赋予针对病毒疾病的保护的有效系统。马铃薯卷叶是在马铃薯植物中进行这种保护的最早疾病之一。但是,到目前为止,尚未报道该保护机制的细节。克隆并测序了阿根廷PLRV菌株的ORF2b,发现与澳大利亚和荷兰菌株的同源性分别为94%和97%。为了阐明针对PLRV感染的保护机制,在35S CaMV启动子和nos终止子的控制下构建了三个版本的ORF2b(不可翻译义,具有工程ATG和反义的可翻译义),并引入了马铃薯植株(cv (Kennebec)由根癌农杆菌介导的转化。嫁接感染实验表明,可以用任何一种构建体获得抗性转基因植物,这表明保护机制与蛋白质的表达无关,并且是RNA介导的。现场试验感染证实获得了抗性转基因事件。使用编码融合蛋白GUS-ORF2b的基因对源自转基因植物的叶片进行生物弹瞬时转化实验,然后对表达GUS的叶斑数量进行评分,这表明该保护作用是由转录后基因沉默机制介导的。

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