Leong K, Lee W, Berk A J
Molecular Biology Institute, University of California, Los Angeles 90024-1570.
J Virol. 1990 Jan;64(1):51-60. doi: 10.1128/JVI.64.1.51-60.1990.
The adenovirus major late promoter (MLP) is active during both the early and late phases of infection. During the early phase the activity of the MLP is similar to those of the other early viral promoters, but during the late phase the rate of transcription from the MLP becomes much greater by comparison. We report here that sequence-specific binding proteins are induced during the late phase which interact with three regions in the first intron of the MLP transcription unit from positions +37 to +68, +80 to +105, and +105 to +125 relative to the transcription initiation site. To measure the significance of these binding sites for transcription during the late phase, we constructed MLP-beta-globin fusions and substituted them for early region 3 in adenovirus recombinants. Deletion of the binding sites caused significant reductions in the rate of transcription, specifically during the late phase of infection. Deletion of all three sites reduced the rate of transcription 25- to 50-fold and the accumulation of cytoplasmic MLP-beta-globin RNA 200-fold. These results indicate that the high rate of transcription from the MLP during the late phase of infection results from the interaction of virus-induced transcription factors with three binding sites in the first intron of the major late transcription unit.
腺病毒主要晚期启动子(MLP)在感染的早期和晚期均具有活性。在早期,MLP的活性与其他早期病毒启动子相似,但相比之下,在晚期MLP的转录速率变得更高。我们在此报告,在晚期诱导出序列特异性结合蛋白,这些蛋白与MLP转录单元第一个内含子中相对于转录起始位点的三个区域相互作用,位置分别为+37至+68、+80至+105和+105至+125。为了衡量这些结合位点在晚期转录中的重要性,我们构建了MLP-β-珠蛋白融合体,并将其替换腺病毒重组体中的早期区域3。结合位点的缺失导致转录速率显著降低,特别是在感染的晚期。所有三个位点的缺失使转录速率降低25至50倍,使细胞质MLP-β-珠蛋白RNA的积累降低200倍。这些结果表明,感染晚期MLP的高转录速率是由病毒诱导的转录因子与主要晚期转录单元第一个内含子中的三个结合位点相互作用所致。