Tebb G, Mattaj I W
European Molecular Biology Laboratory, Heidelberg, FRG.
EMBO J. 1988 Dec 1;7(12):3785-92. doi: 10.1002/j.1460-2075.1988.tb03263.x.
The requirements for the formation of a stable transcription complex on the RNA polymerase II-transcribed Xenopus U2 snRNA gene have been analysed in vivo by oocyte microinjection experiments. The two elements of the U2 promoter which are located in the 5' flanking region of the gene, the DSE and the PSE, are shown to be essential but not sufficient for stable complex formation. Two additional elements are required. The first is a short gene-internal sequence; the second is the nucleotide at the normal point of initiation, which must be a purine. If this nucleotide is changed to a pyrimidine the site of initiation is altered and, concomitantly, the transcription complex formed on the mutant template remains unstable. These results suggest that there is a distinct topological requirement for complex formation which may involve an exact stereospecific alignment of RNA polymerase II with transcription factors bound to the promoter. Despite the apparent involvement of RNA polymerase, transcription per se is not required for complex stability.
通过卵母细胞显微注射实验,在体内分析了在RNA聚合酶II转录的非洲爪蟾U2 snRNA基因上形成稳定转录复合物的要求。位于该基因5'侧翼区域的U2启动子的两个元件,即远端序列元件(DSE)和近端序列元件(PSE),被证明对于稳定复合物的形成是必不可少的,但并不充分。还需要另外两个元件。第一个是短的基因内部序列;第二个是正常起始点的核苷酸,它必须是嘌呤。如果这个核苷酸变成嘧啶,起始位点就会改变,同时,在突变模板上形成的转录复合物仍然不稳定。这些结果表明,复合物形成存在明显的拓扑学要求,这可能涉及RNA聚合酶II与结合在启动子上的转录因子的精确立体特异性排列。尽管明显涉及RNA聚合酶,但转录本身对于复合物的稳定性不是必需的。