Fessler S P, Young C S
Department of Microbiology, Columbia University, New York, New York 10032, USA.
J Virol. 1998 May;72(5):4049-56. doi: 10.1128/JVI.72.5.4049-4056.1998.
The adenovirus gene regulatory program occurs in two distinct phases, as defined by the onset of DNA replication. During the early phase, the E1A, E1B, E2, E3, and E4 genes are maximally expressed, while the major late promoter (MLP) is minimally expressed and transcription is attenuated. After the onset of DNA replication, the IVa2 and pIX genes are expressed at high levels, transcription from the MLP is unattenuated and fully activated, and early gene expression is repressed. Although the cis elements and trans-acting factors responsible for the late-phase activation of the MLP have been identified and characterized and the role of DNA replication in activation has been established, the mechanism(s) underlying the commensurate decrease in early gene expression has yet to be elucidated. The results of this study demonstrate that this decrease depends on a fully functional MLP. Specifically, virus mutants with severely deficient transcription from the MLP exhibit a marked increase in expression of the E1A, E1B, and E2 early genes. These increases were observed at the level of transcription initiation, mRNA accumulation, and protein production. In addition, expression from the late gene pIX, which is not contained within the major late transcription unit (MLTU), is also markedly increased. To begin the analysis of the mechanisms underlying these late-phase effects, mixed-infection experiments with mutant and wild-type viruses were performed. The results show that the effects on early gene expression, as measured both at the protein and RNA levels, are mediated in trans and not in cis. These observations are consistent either with a model in which one or more late protein products encoded by the MLTU acts as a repressor of early gene expression or with one in which the wild-type MLP competes with early promoters for limiting transcription factors.
腺病毒基因调控程序分为两个不同阶段,由DNA复制的起始来界定。在早期阶段,E1A、E1B、E2、E3和E4基因大量表达,而主要晚期启动子(MLP)表达量极低,转录减弱。DNA复制起始后,IVa2和pIX基因高水平表达,MLP的转录不再减弱并被完全激活,早期基因表达受到抑制。尽管已经鉴定并表征了负责MLP晚期激活的顺式元件和反式作用因子,且已确定DNA复制在激活中的作用,但早期基因表达相应降低的机制仍有待阐明。本研究结果表明,这种降低依赖于功能完整的MLP。具体而言,MLP转录严重缺陷的病毒突变体在E1A、E1B和E2早期基因的表达上显著增加。这些增加在转录起始、mRNA积累和蛋白质产生水平均有观察到。此外,主要晚期转录单元(MLTU)中不包含的晚期基因pIX的表达也显著增加。为了开始分析这些晚期效应的潜在机制,进行了突变体和野生型病毒的混合感染实验。结果表明,对早期基因表达的影响,无论是在蛋白质还是RNA水平上测量,都是通过反式作用介导的,而非顺式作用。这些观察结果与以下两种模型之一一致:一种模型是MLTU编码的一种或多种晚期蛋白质产物作为早期基因表达的抑制因子;另一种模型是野生型MLP与早期启动子竞争有限的转录因子。