Huang D H, Roeder R G
Laboratory of Biochemistry and Molecular Biology, Rockefeller University, New York, New York 10021.
Mol Cell Biol. 1988 May;8(5):1906-14. doi: 10.1128/mcb.8.5.1906-1914.1988.
Late in infection, transcription of the EIIa gene is initiated primarily at map unit 72 of the adenovirus genome. A cell-free nuclear extract system was used to determine sequence elements important for the function of this late promoter. In such a system, the transcriptional activity of a circular template was found to be much higher (5- to 10-fold) than that of a linear template. The effect of template topology appeared to be dependent on two distal upstream elements with 5' boundaries located near -265 to -223 and -147 to -133 (in relation to the initiation site), since deletions of these regions reduced transcription of the circular template, in a stepwise fashion, to a level similar to that observed with the linear template. Further deletions revealed an element in the -116 region that appeared to be more important for transcription of the circular template (10-fold reduction) than for transcription of the linear template (3-fold reduction). Lastly, deletion of the TACAAA sequence in the -29 region resulted in further reduction in transcription, indicating that this element functions as a promoter in vitro.
在感染后期,EIIa基因的转录主要起始于腺病毒基因组的图谱单位72处。使用无细胞核提取物系统来确定对该晚期启动子功能重要的序列元件。在这样的系统中,发现环状模板的转录活性比线性模板高得多(5至10倍)。模板拓扑结构的影响似乎取决于两个位于上游远端的元件,其5'边界位于-265至-223和-147至-133附近(相对于起始位点),因为这些区域的缺失会逐步将环状模板的转录降低到与线性模板相似的水平。进一步的缺失揭示了-116区域中的一个元件,该元件对环状模板转录的重要性(降低10倍)似乎比对线性模板转录的重要性(降低3倍)更大。最后,-29区域中TACAAA序列的缺失导致转录进一步降低,表明该元件在体外作为启动子发挥作用。