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The preparation of an infectious full-length cDNA clone of Saffold virus

机译:Saffold病毒感染性全长cDNA克隆的制备

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The pathogenicity of Saffold virus (SAFV) among humans still remains unclear, although it was identified as a novel human cardiovirus in 2007. In order to encourage the molecular pathogenetic studies of SAFV, we generated an infectious cDNA clone of SAFV type 3 (SAFV-3). The present study demonstrated that the synthesis of the full-length infectious RNA by T7 RNA polymerase was terminated by a homologous sequence motif with the human preproparathyroid hormone (PTH) signal in the SAFV-3 genome. To obtain the infectious RNA using T7 promoter, a variant of T7 RNA polymerase, which fails to recognize the PTH signal, was useful. This study will provide a valuable technical insight into the reverse genetics of SAFV.
机译:尽管在2007年被鉴定为新型人心病毒,但尚不清楚人类中是否存在SaffV病毒(SAFV)。为鼓励SAFV的分子致病性研究,我们产生了SAFV 3型(SAFV- 3)。本研究表明,T7 RNA聚合酶可通过SAFV-3基因组中与人甲状旁腺原激素(PTH)信号的同源序列基序终止全长感染性RNA的合成。为了使用T7启动子获得感染性RNA,有用的T7 RNA聚合酶变体无法识别PTH信号。这项研究将为SAFV的反向遗传学提供有价值的技术见解。

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