Incorporation of a central polypurine tract (cPPT) and a posttranscriptional regulatory element (PRE) into lentivirus vectors provides increased transduction efficiency and transgene expression. We compared the effects of these elements individually and together on transduction efficiency and gene expression, using lentivirus vectors pseudotyped with vesicular stomatitis virus G protein (VSV-G) and encoding enhanced green fluorescent protein (GFP) and rat erythropoietin (EPO). The transduction efficiency was greater than 2-fold higher in the vector containing the PRE element, 3-fold higher in vector encoding the cPPT element, and 5-fold increased in the GFP virus containing both cPPT and PRE elements relative to the parent virus. In comparison with parent vector the mean fluorescence intensity (MFI) of GFP expression was 7-fold higher in cells transduced with virus containing PRE, 6-fold increased in cells transduced with virus containing cPPT, and 42-fold increased in GFP-virus containing both cPPT and PRE elements. EPO-virus containing a PRE element showed a nearly 5-fold increase in EPO secretion over the parent vector, and the vector encoding both PRE and cPPT showed a 65-fold increase. Thus, lentivirus vectors incorporating both PRE and cPPT showed expression levels significantly increased over the sum of the components alone, suggesting a synergistic effect.

译文

将慢病毒载体整合到中央多嘌呤区(cPPT)和转录后调控元件(PRE)中,可提高转导效率和转基因表达。我们使用伪装了水泡性口炎病毒G蛋白(VSV-G)并编码增强型绿色荧光蛋白(GFP)和大鼠促红细胞生成素(EPO)的慢病毒载体,比较了这些元素单独以及一起对转导效率和基因表达的影响。相对于亲本病毒,在含有PRE元素的载体中,转导效率高出2倍,在编码cPPT元素的载体中,转导效率高出3倍,在同时含有cPPT和PRE元素的GFP病毒中,转导效率提高了5倍。与亲代载体相比,用含PRE的病毒转导的细胞中GFP表达的平均荧光强度(MFI)高7倍,用含cPPT的病毒转导的细胞中GFP表达的平均荧光强度高6倍,而在含cPPT的病毒转导的细胞中GFP表达的平均荧光强度增加42倍。 cPPT和PRE元素。含有PRE元件的EPO病毒的EPO分泌量比亲本载体增加了近5倍,而编码PRE和cPPT的载体均表现出了65倍的增加。因此,掺有PRE和cPPT的慢病毒载体显示表达水平明显高于单独组分的总和,表明具有协同作用。

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