Shaw A R, Ziff E B
Cell. 1980 Dec;22(3):905-16. doi: 10.1016/0092-8674(80)90568-1.
The major late promoter of adeovirus-2 is located at coordinate 16.45 and initiates synthesis of nuclear precursors that are processed into mRNAs which fall into five 3- co-terminal families, L1-L5. These mRNAs all share a common tripartite 5' leader with a capped terminus encoded at th RNA initiation site. We show that the coorindate 16.45 RNA initiation site is also an early promoter, and yields transcripts detectable as early as 1 hr post-infection, prior to DNA replication and the early-late switch at 6-8 hr. Polyadenylated cytoplasmic RNA from the first 3- co-terminal family, L1, is also produced from the earliest stages of infection. L1 mRNA accumulates in the cytoplasm in the presence of cycloheximide, which blocks DNA replication and the onset of the late phase. Early nuclear RNA contains the same capped 5' terminal RNAase T-1 undecanucleotide and promoter proximal oligonucleotides present in late transcripts. This implies that precisely the same transcription start site is utilized for early L1 mRNA synthesis as is used during the late stage for L1-L5 late mRNA synthesis. In contrast to the early apperance of L1 mRNA, neither L2 nor L3 mRNAs are detected until 5-6 hr post infection. We cnclude that a major event in the Ad-2 early-late switch is a novel form of control which activates L2-L5 mRNA production.
腺病毒-2的主要晚期启动子位于坐标16.45处,启动核前体的合成,这些核前体被加工成mRNA,分为五个3' 共末端家族,即L1-L5。这些mRNA都共享一个共同的三联体5' 前导序列,其帽状末端在RNA起始位点编码。我们发现坐标16.45处的RNA起始位点也是一个早期启动子,在感染后1小时即可检测到转录本,早于DNA复制以及6-8小时的早期-晚期转换。来自第一个3' 共末端家族L1的多聚腺苷酸化细胞质RNA也在感染的最早阶段产生。在存在环己酰亚胺的情况下,L1 mRNA在细胞质中积累,环己酰亚胺可阻断DNA复制和晚期阶段的开始。早期核RNA包含与晚期转录本中相同的帽状5' 末端核糖核酸酶T-1十一核苷酸和启动子近端寡核苷酸。这意味着早期L1 mRNA合成所利用的转录起始位点与晚期L1-L5晚期mRNA合成所使用的转录起始位点完全相同。与L1 mRNA的早期出现相反,直到感染后5-6小时才检测到L2和L3 mRNA。我们得出结论,腺病毒-2早期-晚期转换中的一个主要事件是一种新的控制形式,它激活L2-L5 mRNA的产生。