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Gene Expression and Regulation from the p7 Promoter of Aedes Densonucleosis Virus

机译:伊蚊核糖核酸病毒p7启动子的基因表达与调控

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摘要

The nonstructural proteins NS1 and NS2 are thought to be expressed from the p7 promoter of Aedes densonucleosis virus (AeDNV). To study gene expression from the p7 promoter, eight different plasmids were constructed by fusing β-galactosidase or β-glucuronidase into the genome so that the reporter gene was in different open reading frames and under the transcriptional control of the p7 promoter. After transfection into C6/36 Aedes albopictus cells, constructs generated comparable amounts of RNA, but only the NS1 and NS2 fusion constructs produced appreciable levels of active enzyme. NS1 and NS2 fusion constructs contained wild-type AeDNV sequences from the p7 promoter downstream to nucleotide 458. The remaining constructs, with the exception of p7GUS.rf3, lacked some or all of these necessary sequences and inefficiently produced protein. These data suggest that sequences downstream of the p7 promoter play a role in translational regulation of gene expression from the p7 promoter of AeDNV.
机译:非结构蛋白NS1和NS2被认为是从伊蚊伊蚊核糖核酸病毒(AeDNV)的p7启动子表达的。为了研究p7启动子的基因表达,通过将β-半乳糖苷酶或β-葡萄糖醛酸苷酶融合到基因组中,构建了八个不同的质粒,从而使报告基因处于不同的开放阅读框内,并处于p7启动子的转录控制之下。转染到C6 / 36白纹伊蚊细胞中后,构建体产生了相当数量的RNA,但只有NS1和NS2融合构建体产生了可观水平的活性酶。 NS1和NS2融合构建体包含从p7启动子下游到458核苷酸的野生型AeDNV序列。除p7GUS.rf3之外,其余构建体缺少某些或全部这些必需序列,并且蛋白质生产效率低下。这些数据表明,p7启动子下游的序列在AeDNV的p7启动子的基因表达的翻译调节中起作用。

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