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A cryptic promoter in potato virus X vector interrupted plasmid construction

机译:马铃薯X病毒载体中的一个秘密启动子中断了质粒的构建

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摘要

Background: Potato virus X has been developed into an expression vector for plants. It is widely used to express foreign genes. In molecular manipulation, the foreign genes need to be sub-cloned into the vector. The constructed plasmid needs to be amplified. Usually, during amplification stage, the foreign genes are not expressed. However, if the foreign gene is expressed, the construction work could be interrupted. Two different viral genes were sub-cloned into the vector, but only one foreign gene was successfully sub-cloned. The other foreign gene, canine parvovirus type 2 (CPV- 2) VP1 could not be sub-cloned into the vector and amplified without mutation (frame shift mutation). Results: A cryptic promoter in the PVX vector was discovered with RT-PCR. The promoter activity was studied with Northern blots and Real-time RT-PCR. Conclusion: It is important to recognize the homologous promoter sequences in the vector when a virus is developed as an expression vector. During the plasmid amplification stage, an unexpected expression of the CPV-2 VP1 gene (not in the target plants, but in E. coli) can interrupt the downstream work.
机译:背景:马铃薯X病毒已发展成为植物表达载体。它被广泛用于表达外源基因。在分子操作中,需要将外源基因亚克隆到载体中。构建的质粒需要扩增。通常,在扩增阶段,不表达外源基因。但是,如果表达外源基因,则可能会中断构建工作。将两个不同的病毒基因亚克隆到载体中,但是仅成功地亚克隆了一个外源基因。另一个外源基因,犬细小病毒2型(CPV-2)VP1不能亚克隆到载体中并扩增而没有突变(移码突变)。结果:通过RT-PCR在PVX载体中发现了一个秘密启动子。用Northern印迹和实时RT-PCR研究启动子活性。结论:将病毒开发为表达载体时,识别载体中的同源启动子序列很重要。在质粒扩增阶段,CPV-2 VP1基因的意外表达(不在目标植物中,但在大肠杆菌中)会中断下游工作。

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