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一个包含HCVIRES的高效真核双顺反子表达载体的构建

机译:一个包含HCVIRES的高效真核双顺反子表达载体的构建

摘要

In this paper, a new eukaryotic bi-cistronic expression vector containing Hepatitis C Virus(HCV) internal ribosome entry site (IRES) expressing two foreign genes from one mRNA was constructed. The sequence starting from the 5' untranslated region of 18nt to 32nt in HCV core coding region was cloned and then the encephalomyocarditis virus (ECMV) IRES sequence in the commercial vector pIRES was substituted to construct a new vector pCVIR. Green fluorescent protein (GFP) and Hepatitis B virus surface antigen (HBsAg) coding genes were inserted up-stream and down-stream of IRES sequence. The fluorescence intensity of GFP and HBsAg were determined by flow cytometry and ELISA respectively., thus, the expression efficiency of the two vectors, pCVIR and pIRES could be compared. The experimental results showed that the vector pCVIR could translate the GFP and HBsAg genes down-stream of its HCV IRES sequence more efficiently without impairing the expression of genes up-stream of IRES sequence than the vector pIRES.It is...
机译:本文构建了一种新的真核生物双顺反子表达载体,该载体包含丙型肝炎病毒(HCV)内部核糖体进入位点(IRES),可从一个mRNA表达两个外源基因。克隆了HCV核心编码区中从18nt的5'非翻译区到32nt的序列,然后替换了商业载体pIRES中的脑心肌炎病毒(ECMV)IRES序列以构建新的载体pCVIR。将绿色荧光蛋白(GFP)和乙型肝炎病毒表面抗原(HBsAg)编码基因插入到IRES序列的上游和下游。通过流式细胞术和ELISA分别测定了GFP和HBsAg的荧光强度,从而可以比较两种载体pCVIR和pIRES的表达效率。实验结果表明,与载体pIRES相比,载体pCVIR可以更有效地翻译其HCV IRES序列下游的GFP和HBsAg基因,而不会损害IRES序列上游的基因表达。

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