Tse-Dinh Y C, Beran R K
E. I. du Pont de Nemours and Co. Central Research and Development Department, Wilmington, DE 19898.
J Mol Biol. 1988 Aug 20;202(4):735-42. doi: 10.1016/0022-2836(88)90554-2.
There are four transcriptional promoters present in the 5' control region of the Escherichia coli DNA topoisomerase I (topA) gene. These were identified with Bal31 nuclease-generated deletions and mapping of the 5' ends of the mRNAs with avian reverse transcriptase. Recombinant plasmids with all or some of these promoters fused to the galactokinase (galK) gene-coding region have been constructed and used to study transcription from the promoters both in vitro and in vivo. The promoter (P1) closest to the starting ATG codon has a near consensus -35 sequence (GTTGATA) but unusual -10 (CATATCG) sequence. The other three promoters (P2, P3 and P4) are clustered together 60 base-pairs further upstream. Negative DNA supercoiling is required for efficient transcription from P1, P1 + P2 + P3 + P4, P2 + P3 + P4, P3 + P4 and P4 alone. The combination of all four promoters demonstrates greater supercoiling dependence than does any of the other subsets tested.
大肠杆菌DNA拓扑异构酶I(topA)基因的5'控制区域存在四个转录启动子。这些启动子是通过Bal31核酸酶产生的缺失以及用禽逆转录酶对mRNA的5'末端进行定位来确定的。已经构建了将所有或部分这些启动子与半乳糖激酶(galK)基因编码区域融合的重组质粒,并用于在体外和体内研究启动子的转录。最接近起始ATG密码子的启动子(P1)具有接近一致的-35序列(GTTGATA),但-10序列(CATATCG)不寻常。其他三个启动子(P2、P3和P4)聚集在更上游60个碱基对处。仅从P1、P1 + P2 + P3 + P4、P2 + P3 + P4、P3 + P4和P4进行有效转录需要负DNA超螺旋。与任何其他测试的子集相比,所有四个启动子的组合表现出更大的超螺旋依赖性。