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Plasmids driven minigenome rescue system for Newcastle disease virus V4 strain

机译:新城疫病毒V4株的质粒驱动微型基因组拯救系统

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We establish a plasmid-driven minigenome system for Newcastle disease virus (NDV) V4 strain. Unlike the previously reported T7 polymerase based rescue system for Mononegavirales, the developed strategy does not necessitate the introduction of exogenous T7 polymerase by helper virus or stably expressing cell lines. This was achieved by transfection of plasmid pCAGGS-T7. The open reading frame (ORF) of enhanced green-fluorescent protein (EGFP) gene was inserted into constructed minigenome system pBRT7-mini and has been successfully expressed. Further packaging experiments indicate that 3′ end leader and 5′ end trailer regions are important for replication, transcription and packaging.
机译:我们建立了新城疫病毒(NDV)V4株的质粒驱动的微型基因组系统。与以前报道的基于Monogavirales的基于T7聚合酶的拯救系统不同,该开发的策略无需通过辅助病毒或稳定表达的细胞系引入​​外源性T7聚合酶。这是通过转染质粒pCAGGS-T7实现的。将增强的绿色荧光蛋白(EGFP)基因的开放阅读框(ORF)插入构建的微型基因组系统pBRT7-mini中,并已成功表达。进一步的包装实验表明3'末端前导区和5'末端尾区对于复制,转录和包装很重要。

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