Chen D, Lilley D M
Department of Biochemistry, The University of Dundee, Dundee, DD1 4HN, UK.
J Mol Biol. 1999 Jan 15;285(2):443-8. doi: 10.1006/jmbi.1998.2358.
Transcription can induce high levels of negative supercoiling into plasmid DNA under some circumstances. This is especially true when the plasmid carries a functional tetracycline-resistance gene tetA, and is borne in a topA strain of Escherichia coli or Salmonella typhimurium. An important mechanism in transcription-induced supercoiling is believed to be the twin supercoiled-domain effect resulting from hindered rotation of the transcriptional complex, and this is very much more efficient where there is coupled transcription, translation and membrane insertion of the gene product. However, we have noted that strong promoters inserted into tetA-carrying plasmids can greatly increase the fraction of hypersupercoiled DNA. We show here that this effect is clearly present when the inserted promoter transcribes a very short segment of DNA (down to transcript lengths of approximately 45 nt), and where there is no possibility of translation of the RNA transcript. We suggest that the repeated helical opening due to transcriptional initiation is a significant contributor to the induction of high levels of supercoiling.
在某些情况下,转录可在质粒DNA中诱导产生高水平的负超螺旋。当质粒携带功能性四环素抗性基因tetA,并存在于大肠杆菌或鼠伤寒沙门氏菌的topA菌株中时,情况尤其如此。转录诱导超螺旋的一个重要机制被认为是转录复合物旋转受阻导致的双超螺旋结构域效应,并且在基因产物进行偶联转录、翻译和膜插入时,这种效应效率更高。然而,我们注意到插入携带tetA质粒的强启动子可大大增加超螺旋DNA的比例。我们在此表明,当插入的启动子转录非常短的DNA片段(转录本长度低至约45 nt)且RNA转录本不可能进行翻译时,这种效应明显存在。我们认为转录起始导致的重复螺旋解开是诱导高水平超螺旋的一个重要因素。