Hashimoto S, Green M
Nucleic Acids Res. 1984 Dec 11;12(23):9067-82. doi: 10.1093/nar/12.23.9067.
The 5'-terminal structures of human adenovirus type 2 (Ad2) early region 2 (E2) mRNA were investigated. The E2 transcription unit has several interesting properties, including the presence of a TATA-like box that matches the consensus sequence poorly, delayed transcription during early stages of infection, and a switch in promoter recognition late after infection. E2-specific RNA, 5'-labeled in vitro to high specific activity was analyzed. Purified E2 mRNA was digested with RNase A or RNase T1 and the resulting oligonucleotides were resolved by two dimensional paper electrophoresis-homochromatography. Remarkably, as many as sixteen 5'-terminal RNase A oligonucleotides were identified and their sequences were deduced. The most common 5'-termini in the RNase A digest were p(m6)AmCp, p(m6)AmA(m)Cp, pGmA(m)Cp, and p(m6)AmG(m)Cp. Two RNase A oligonucleotides originated from the E4 promoter region, consistent with electron microscopic observations. The sequence encoding these potential initiation sites covered about 90 nucleotides. Eleven of the sequences of the 5'-terminal RNase A oligonucleotides were aligned with the Ad2 DNA sequence in the Ad2 E2 promoter region. If the heterogeneous termini in the E2 promoter region were generated by a process of transcription initiation, their existence cannot be explained by stuttering of RNA polymerase II. This suggests that the transcription of Ad early region 2 has features which differ from those of other Ad2 early gene transcription units. Perhaps this is due to the absence of a conventional TATA box which is believed to position the initiation site. Alternatively, it is conceivable that the E2 promoter represents an alternate class of RNA polymerase II promoters containing different signals with different requirements for activation and/or that an E1A gene product modifies transcription initiation.
对人2型腺病毒(Ad2)早期区域2(E2)mRNA的5′末端结构进行了研究。E2转录单元具有几个有趣的特性,包括存在一个与共有序列匹配较差的类TATA框、感染早期转录延迟以及感染后期启动子识别的转换。分析了体外5′端标记至高比活性的E2特异性RNA。用核糖核酸酶A或核糖核酸酶T1消化纯化的E2 mRNA,所得寡核苷酸通过二维纸电泳-同系层析法进行分离。值得注意的是,鉴定出多达16种5′末端核糖核酸酶A寡核苷酸,并推导了它们的序列。核糖核酸酶A消化产物中最常见的5′末端是p(m6)AmCp、p(m6)AmA(m)Cp、pGmA(m)Cp和p(m6)AmG(m)Cp。两种核糖核酸酶A寡核苷酸起源于E4启动子区域,这与电子显微镜观察结果一致。编码这些潜在起始位点的序列覆盖约90个核苷酸。5′末端核糖核酸酶A寡核苷酸的11个序列与Ad2 E2启动子区域的Ad2 DNA序列比对。如果E2启动子区域的异质末端是由转录起始过程产生的,那么RNA聚合酶II的口吃现象无法解释它们的存在。这表明Ad早期区域2的转录具有与其他Ad2早期基因转录单元不同的特征。也许这是由于缺乏一个被认为定位起始位点的传统TATA框。或者,可以想象E2启动子代表了一类不同的RNA聚合酶II启动子,其包含不同的信号,对激活有不同的要求,和/或E1A基因产物修饰转录起始。