Glenn G M, Ricciardi R P
Wistar Institute, Philadelphia, PA 19104.
Virus Res. 1988 Jan;9(1):73-91. doi: 10.1016/0168-1702(88)90051-2.
The appearance and steady-state accumulation of specific viral RNAs during the early phase of adenovirus type 5 (Ad5) infection was examined. HeLa cells were synchronously infected and harvested at 30 min intervals throughout the first 12 h of infection. Total cytoplasmic RNA was extracted from infected cells and analyzed by hybridization-selection and translation to identify the viral mRNAs from each early region on the basis of the protein products they encode. The same RNA samples were used for S-1 nuclease and Northern blot analyses to quantitatively compare the levels of individual viral RNAs that accumulate within each early transcription region (E1A, E1B, L1, E2A, E3 and E4). The salient features of this analysis show that RNA accumulation occurs first from E1A followed by E2A, E3 and E4, E1B and lastly, L1. Although the profile of RNA accumulation was unique for each early region, overlapping RNAs within E1A, E3, and E4, respectively, remained generally parallel to one another throughout early infection, in contrast to RNAs from E1B and L1, respectively. Since both the appearance and quantitative accumulation of specific early viral mRNAs were examined at many time points, a number of subtleties associated with the complex dynamics of early Ad5 gene expression were revealed. In particular, the L1 region was shown to transcribe from the major late promoter two early RNAs of 3.81 Kb and 3.5 Kb, either or both of which encode the 52,55 kDa proteins; the auxiliary i leader sequence was found on the 3.81 Kb RNA but not on the 3.5 Kb RNA.
研究了5型腺病毒(Ad5)感染早期特定病毒RNA的出现及稳态积累情况。HeLa细胞被同步感染,并在感染的前12小时内每隔30分钟收获一次。从感染细胞中提取总细胞质RNA,通过杂交选择和翻译进行分析,以根据它们编码的蛋白质产物鉴定来自每个早期区域的病毒mRNA。相同的RNA样本用于S-1核酸酶和Northern印迹分析,以定量比较每个早期转录区域(E1A、E1B、L1、E2A、E3和E4)内积累的单个病毒RNA的水平。该分析的显著特征表明,RNA积累首先从E1A开始,接着是E2A、E3和E4、E1B,最后是L1。尽管每个早期区域的RNA积累模式是独特的,但与E1B和L1的RNA不同,E1A、E3和E4内的重叠RNA在早期感染期间总体上彼此保持平行。由于在多个时间点检查了特定早期病毒mRNA的出现和定量积累,揭示了许多与Ad5早期基因表达复杂动力学相关的细微之处。特别是,L1区域被证明从主要晚期启动子转录出3.81 Kb和3.5 Kb的两种早期RNA,其中一种或两种都编码52、55 kDa蛋白;在3.81 Kb RNA上发现了辅助性i前导序列,但在3.5 Kb RNA上未发现。