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转录因子C/EBP与乙型肝炎病毒的增强子元件II结合并使其反式激活。

Transcriptional factor C/EBP binds to and transactivates the enhancer element II of the hepatitis B virus.

作者信息

López-Cabrera M, Letovsky J, Hu K Q, Siddiqui A

机构信息

Department of Microbiology and Immunology, Biochemistry, Biophysics and Genetics, University of Colorado School of Medicine, Denver 80262.

出版信息

Virology. 1991 Aug;183(2):825-9. doi: 10.1016/0042-6822(91)91019-d.

Abstract

The human hepatitis B Virus genome (HBV) contains a liver-specific enhancer upstream of the X ORF which has been studied in detail by several investigators. A second liver-specific enhancer element, designated here as enhancer II, has been relatively recently described in the HBV genome, which is located within the core/pregenomic promoter. We have studied the interactions of transcriptional factors with this element and show here that the nuclear factor CCAAT/enhancer binding protein (C/EBP) binds at a unique site within these sequences. Further, using the transient cotransfection scheme of expression with C/EBP encoding vectors and an enhancer II-reporter gene construct, we demonstrate that the enhancer element II responds to increasing amounts of C/EBP by displaying transactivation. Evidence for the functional role of the enhancer element II in transcriptional regulation of the HBV gene expression is presented. A major influence of the enhancer II appears to be on the surface antigen expression.

摘要

人类乙型肝炎病毒基因组(HBV)在X开放阅读框上游含有一个肝脏特异性增强子,几位研究人员已对其进行了详细研究。第二个肝脏特异性增强子元件,在此处命名为增强子II,是最近在HBV基因组中发现的,它位于核心/前基因组启动子内。我们研究了转录因子与该元件的相互作用,在此表明核因子CCAAT/增强子结合蛋白(C/EBP)在这些序列中的一个独特位点结合。此外,通过使用表达C/EBP编码载体与增强子II报告基因构建体的瞬时共转染方案,我们证明增强子元件II通过显示反式激活对增加量的C/EBP作出反应。本文提供了增强子元件II在HBV基因表达转录调控中功能作用的证据。增强子II的主要影响似乎在于表面抗原的表达。

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