Shaul Y, Rutter W J, Laub O
EMBO J. 1985 Feb;4(2):427-30. doi: 10.1002/j.1460-2075.1985.tb03646.x.
Fragments of the cloned hepatitis B virus (HBV) genome were assayed in vivo for the presence of a transcriptional enhancer element. We demonstrate that sequences positioned approximately 450 bp upstream from the HBcAg gene promoter are required for its efficient activity. These HBV stimulatory sequences activate transcription when inserted upstream to a heterologous SV40 early promoter. Like other known enhancer elements, this HBV sequence acts in an orientation-independent manner. Furthermore, the HBV enhancer element exhibits a preferred activity in a human hepatoma cell line.
对克隆的乙型肝炎病毒(HBV)基因组片段进行体内检测,以确定转录增强子元件的存在。我们证明,位于HbcAg基因启动子上游约450 bp处的序列是其高效活性所必需的。当这些HBV刺激序列插入到异源SV40早期启动子上游时,可激活转录。与其他已知的增强子元件一样,该HBV序列以方向独立的方式发挥作用。此外,HBV增强子元件在人肝癌细胞系中表现出优先活性。