Pan G, Greenblatt J
Banting and Best Department of Medical Research, University of Toronto, Canada.
J Biol Chem. 1994 Dec 2;269(48):30101-4.
To further elucidate the mechanism of transcriptional initiation, we used synthetic oligonucleotides to prepare templates containing heteroduplex regions of varying size and location along the DNA of the adenovirus major late promoter. Unlike closed, linear DNA, or DNA with a downstream mismatch, DNA with a mismatch upstream of the initiation site only required the general factors TATA box-binding protein and transcription factor (TF) IIB to direct specific and accurate initiation in vitro by calf thymus RNA polymerase II. In the presence of TFIIF, initiation was possible on closed, linear DNA, but an upstream mismatch region still stimulated transcriptional initiation by more than 100-fold, leading to production of approximately 0.5 transcript/template in the absence of TFIIE, TFIIH, or ATP. The presence of a DNA mismatch was most effective in the -9 to -1 region; furthermore, stimulation by a mismatch did not require that the initiation site be included in the heteroduplex region. Efficient initiation at the immunoglobulin heavy chain promoter in the presence of TATA box-binding protein and TFIIB was also achieved when a mismatch region was introduced from -9 to +3. Our results suggest that initiation by RNA polymerase II in the absence of transcriptional activation is limited by melting of the promoter DNA upstream of the initiation site.
为了进一步阐明转录起始的机制,我们使用合成寡核苷酸制备模板,这些模板含有沿腺病毒主要晚期启动子DNA不同大小和位置的异源双链区域。与封闭的线性DNA或具有下游错配的DNA不同,起始位点上游有错配的DNA仅需要通用因子TATA框结合蛋白和转录因子(TF)IIB,就能在体外通过小牛胸腺RNA聚合酶II指导特异性和准确的起始。在TFIIF存在的情况下,封闭的线性DNA上也可能起始转录,但上游错配区域仍能将转录起始刺激100倍以上,在没有TFIIE、TFIIH或ATP的情况下,导致每个模板产生约0.5个转录本。DNA错配在-9至-1区域最为有效;此外,错配的刺激并不要求起始位点包含在异源双链区域中。当从-9至+3引入错配区域时,在TATA框结合蛋白和TFIIB存在的情况下,免疫球蛋白重链启动子处也能实现高效起始。我们的结果表明,在没有转录激活的情况下,RNA聚合酶II的起始受起始位点上游启动子DNA解链的限制。