Zajchowski D A, Jalinot P, Kedinger C
Laboratoire de Génétique Moléculaire des Eucaryotes du CNRS, Faculté de Médecine, Strasbourg, France.
J Virol. 1988 May;62(5):1762-7. doi: 10.1128/JVI.62.5.1762-1767.1988.
The transcriptional induction of adenovirus early genes by the viral immediate early gene EIa constitutes an attractive model system for the study of control mechanisms involved in eucaryotic promoter function. The EIa-mediated activation of the divergently transcribed EIIa early (EIIaE) and EIII promoters was investigated in experiments in which recombinant plasmids containing the entire EIIa-EIII control region were cotransfected with a plasmid expressing the EIa 13S mRNA. First, both promoters were activated by low levels of EIa, but the extent of EIII induction decreased with increasing EIa concentrations, whereas EIIaE stimulation remained unchanged. Second, transcriptional analysis of deletion mutants revealed that an element of the EIIaE promoter contributed to maximal EIa responsiveness of the nearby EIII promoter. This element, located between positions -82 and -71 with respect to the EIIaE major cap site, corresponded to the central portion of an EIa-dependent enhancer, originally mapped between about -110 and -50 (P. Jalinot and C. Kédinger, Nucleic Acids Res. 14:2651-2669, 1986). The implication of these observations in the coordinate expression from the EIIaE and EIII promoters during lytic infection is discussed.
病毒即刻早期基因E1a对腺病毒早期基因的转录诱导,构成了一个用于研究真核启动子功能相关调控机制的引人注目的模型系统。在实验中,研究了E1a介导的对反向转录的EIIa早期(EIIaE)和EIII启动子的激活作用,实验中将含有整个EIIa - EIII控制区的重组质粒与表达E1a 13S mRNA的质粒共转染。首先,两个启动子都被低水平的E1a激活,但随着E1a浓度增加,EIII的诱导程度降低,而EIIaE的刺激作用保持不变。其次,对缺失突变体的转录分析表明,EIIaE启动子的一个元件对附近EIII启动子的最大E1a反应性有贡献。这个元件相对于EIIaE主要帽位点位于 - 82至 - 71位之间,对应于一个E1a依赖性增强子的中心部分,最初定位在约 - 110至 - 50之间(P. Jalinot和C. Kédinger,《核酸研究》14:2651 - 2669,1986)。讨论了这些观察结果对裂解感染期间EIIaE和EIII启动子协同表达的影响。