Depto A S, Stenberg R M
Department of Microbiology and Immunology, West Virginia University Health Sciences Center, Morgantown 26506.
J Virol. 1989 Mar;63(3):1232-8. doi: 10.1128/JVI.63.3.1232-1238.1989.
To better understand the regulation of late gene expression in human cytomegalovirus (CMV)-infected cells, we examined expression of the gene that codes for the 65-kilodalton lower-matrix phosphoprotein (pp65). Analysis of RNA isolated at 72 h from cells infected with CMV Towne or ts66, a DNA-negative temperature-sensitive mutant, supported the fact that pp65 is expressed at low levels prior to viral DNA replication but maximally expressed after the initiation of viral DNA replication. To investigate promoter activation in a transient expression assay, the pp65 promoter was cloned into the indicator plasmid containing the gene for chloramphenicol acetyltransferase (CAT). Transfection of the promoter-CAT construct and subsequent superinfection with CMV resulted in activation of the promoter at early times after infection. Cotransfection with plasmids capable of expressing immediate-early (IE) proteins demonstrated that the promoter was activated by IE proteins and that both IE regions 1 and 2 were necessary. Analysis of promoter deletion mutants indicated that the 5' minimal sequence required for activation is -61 from the CAP site (+1) and that an 8-base-pair sequence located at -51 to -58 is necessary for activation of the pp65 promoter. This sequence is repeated once at +93 and is found as an inverted repeat at +67. These studies suggest that interactions between IE proteins and this octamer sequence may be important for the regulation and expression of this CMV gene.
为了更好地理解人巨细胞病毒(CMV)感染细胞中晚期基因表达的调控机制,我们检测了编码65千道尔顿低基质磷蛋白(pp65)的基因的表达情况。对感染CMV Towne株或ts66(一种DNA阴性温度敏感突变株)72小时后分离得到的RNA进行分析,证实了pp65在病毒DNA复制前表达水平较低,但在病毒DNA复制起始后大量表达这一事实。为了在瞬时表达试验中研究启动子激活情况,将pp65启动子克隆到含有氯霉素乙酰转移酶(CAT)基因的指示质粒中。将启动子-CAT构建体转染细胞,随后用CMV进行超感染,结果显示在感染后早期启动子被激活。与能够表达即刻早期(IE)蛋白的质粒共转染表明,启动子被IE蛋白激活,且IE区域1和2均是必需的。对启动子缺失突变体的分析表明,激活所需的5'最小序列位于距CAP位点(+1)-61处,且位于-51至-58的一个8碱基对序列对于pp65启动子的激活是必需的。该序列在+93处重复一次,并在+67处以反向重复形式存在。这些研究表明,IE蛋白与该八聚体序列之间的相互作用可能对该CMV基因的调控和表达至关重要。