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利用生物发光成像评价乙型肝炎病毒启动子在小鼠体内的持续转基因表达。

Evaluation of hepatitis B virus promoters for sustained transgene expression in mice by bioluminescence imaging.

机构信息

Beijing Institute of Transfusion Medicine, Tai ping Road 27#, Beijing 100850, China.

出版信息

Virus Res. 2010 May;149(2):162-6. doi: 10.1016/j.virusres.2010.01.012. Epub 2010 Feb 1.

Abstract

To find new liver-specific expression cassettes for long-term expression of therapeutic genes in the context of pDNA, the function and specificity of hepatitis B virus (HBV)' two hepatic enhancers (EnI and EnII), combined with HBV core and X promoters in cultured cells were evaluated. By bioluminescence imaging and hydrodynamic gene transfer technology, the persistence of transgene expression containing these regulatory sequences in the liver of mice was assessed. Our data indicated that both HBV enhancers were able to stimulate HBV core and X promoter activity in cultured cells of hepatic origin. In vivo, HBV core promoter linked to EnI and EnII (EII-EI-Pc) and X promoter linked to EnI and EnII (EI-EII-Px) could direct a constant and high-level gene expression.

摘要

为了在 pDNA 背景下找到用于治疗基因长期表达的新的肝脏特异性表达盒,评估了乙型肝炎病毒 (HBV) 的两个肝增强子 (EnI 和 EnII) 以及 HBV 核心和 X 启动子的功能和特异性,在培养的细胞中。通过生物发光成像和水力基因转移技术,评估了含有这些调节序列的转基因在小鼠肝脏中的持续表达。我们的数据表明,HBV 增强子均能刺激肝源培养细胞中 HBV 核心和 X 启动子的活性。在体内,与 EnI 和 EnII 相连的 HBV 核心启动子 (EII-EI-Pc) 和与 EnI 和 EnII 相连的 X 启动子 (EI-EII-Px) 可指导恒定的高水平基因表达。

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