Lo W Y, Ting L P
Graduate Institute of Microbiology and Immunology, National Yang-Ming Medical College, Shih-Pai, Taipei, Taiwan, Republic of China.
J Virol. 1994 Mar;68(3):1758-64. doi: 10.1128/JVI.68.3.1758-1764.1994.
Enhancer II of human hepatitis B virus has dual functions in vivo. Located at nucleotides (nt) 1646 to 1741, it can stimulate the surface and X promoters from a downstream position. Moreover, the same sequence can also function as upstream regulatory element that activates the core promoter in a position- and orientation-dependent manner. In this study, we report the identification and characterization of a negative regulatory element (NRE) upstream of enhancer II (nt 1613 to 1636) which can repress both the enhancer and upstream stimulatory function of the enhancer II sequence in differentiated liver cells. This NRE has marginal inhibitory effect by itself but a strong repressive function in the presence of a functional enhancer II. Mutational analysis reveals that sequence from nt 1616 to 1621 is required for repression of enhancer activity by the NRE. Gel shift analysis reveals that this negative regulatory region can be recognized by a specific protein factor(s) present at the 0.4 M NaCl fraction of HepG2 nuclear extracts. The discovery of the NRE indicates that HBV gene transcription is controlled by combined effects of both positive and negative regulation. It also provides a unique system with which to study the mechanism of negative regulation of gene expression.
人类乙型肝炎病毒增强子II在体内具有双重功能。它位于核苷酸(nt)1646至1741处,能够从下游位置刺激表面启动子和X启动子。此外,相同序列还可作为上游调控元件,以位置和方向依赖的方式激活核心启动子。在本研究中,我们报告了增强子II上游(nt 1613至1636)一个负调控元件(NRE)的鉴定和特征,该元件可在分化的肝细胞中抑制增强子II序列的增强子功能和上游刺激功能。该NRE自身具有微弱的抑制作用,但在存在功能性增强子II时具有强大的抑制功能。突变分析表明,NRE抑制增强子活性需要nt 1616至1621的序列。凝胶迁移分析表明,该负调控区域可被存在于HepG2细胞核提取物0.4M NaCl组分中的一种特定蛋白质因子识别。NRE的发现表明,乙肝病毒基因转录受正调控和负调控的联合作用控制。它还提供了一个独特的系统来研究基因表达负调控的机制。