Rosa M D
Cell. 1979 Apr;16(4):815-25. doi: 10.1016/0092-8674(79)90097-7.
The DNA sequences of four promoters for the bacteriophage-specified T7 RNA polymerase have been determined. All four regions contain an identical 23 bp sequence 5' pTAATACGACTCACTATAGGGAG-A(oh) which includes the 17 bp prior to and the first 6 bp of the transcribed region. They are located at 46.5, 55, 57 and 87% on the standard T7 map, thereby corresponding to the in vitro T7 class III RNA species IIIa, IV, V and IIIb, respectively. The precise RNA initiation sites were determined by 5' terminal RNA sequence analysis of the transcripts synthesized from promoter-containing DNA fragments. The comparative properties of these promoters for the monomeric T7 RNA polymerase and those for the multimeric E. coli RNA polymerase are discussed.
噬菌体特异性T7 RNA聚合酶的四个启动子的DNA序列已被确定。所有四个区域都包含一个相同的23 bp序列5' pTAATACGACTCACTATAGGGAG-A(oh),其中包括转录区域之前的17 bp和转录区域的前6 bp。它们位于标准T7图谱上的46.5%、55%、57%和87%处,因此分别对应于体外T7 III类RNA物种IIIa、IV、V和IIIb。通过对含启动子的DNA片段合成的转录本进行5'末端RNA序列分析,确定了精确的RNA起始位点。讨论了这些启动子对单体T7 RNA聚合酶和多聚体大肠杆菌RNA聚合酶的比较特性。