Lamond A I
EMBO J. 1985 Feb;4(2):501-7. doi: 10.1002/j.1460-2075.1985.tb03656.x.
The effect of DNA supercoiling on transcription of a bacterial tRNA gene has been analysed in vitro and in vivo. The Escherichia coli tyrT gene is found to be completely dependent on negative supercoiling when transcription is assayed in vitro at physiological salt concentrations and this supercoiling dependence is shown to be a property of the primary promoter sequences. The supercoiling sensitivity can however be removed by reducing the salt concentration below 50 mM KCl. The effect of supercoiling in vivo was analysed by measuring the activity of the tyrT promoter on a galK fusion vector in E. coli strains that have mutations in either the DNA gyrase or topoisomerase I genes. Surprisingly, in view of the dramatic in vitro effects, supercoiling could be either increased or decreased relative to the wild-type in vivo level without causing any change in tyrT promoter activity.
已在体外和体内分析了DNA超螺旋对细菌tRNA基因转录的影响。当在生理盐浓度下进行体外转录测定时,发现大肠杆菌tyrT基因完全依赖于负超螺旋,并且这种超螺旋依赖性被证明是初级启动子序列的一个特性。然而,通过将盐浓度降低到50 mM KCl以下,可以消除超螺旋敏感性。通过测量tyrT启动子在DNA促旋酶或拓扑异构酶I基因发生突变的大肠杆菌菌株中的galK融合载体上的活性,分析了体内超螺旋的影响。令人惊讶的是,鉴于体外的显著影响,相对于野生型体内水平,超螺旋在体内可以增加或减少,而不会引起tyrT启动子活性的任何变化。