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Inhibition of the gyrA promoter by transcription-coupled DNA supercoiling in Escherichia coli

机译:转录偶联DNA超螺旋在大肠杆菌中对gyrA启动子的抑制

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摘要

The E. coli gyrA promoter (PgyrA) is a DNA supercoiling sensitive promoter, stimulated by relaxation of DNA templates, and inhibited by (−) DNA supercoiling in bacteria. However, whether PgyrA can be inhibited by transient and localized transcription-coupled DNA supercoiling (TCDS) has not been fully examined. In this paper, using different DNA templates including the E. coli chromosome, we show that transient and localized TCDS strongly inhibits PgyrA in E. coli. This result can be explained by a twin-supercoiled domain model of transcription in which (+) and (−) supercoiled domains are generated around the transcribing RNA polymerase. We also find that fluoroquinolones, such as ciprofloxacin, can substantially increase the expression of the firefly luciferase under the control of the PgyrA coupled to a divergent IPTG-inducible promoter in the presence of IPTG. This stimulation of PgyrA by fluoroquinolones can be also explained by the twin-supercoiled domain model of transcription. This unique property of TCDS may be configured into a high throughput-screening (HTS) assay to identify antimicrobial compounds targeting bacterial DNA gyrase.
机译:大肠杆菌gyrA启动子(PgyrA)是DNA超螺旋敏感的启动子,可通过DNA模板的松弛来刺激,并被细菌中的(-)DNA超螺旋抑制。但是,尚未完全检查PgyrA是否可以被瞬时和局部转录偶联DNA超螺旋(TCDS)抑制。在本文中,我们使用包括大肠杆菌染色体在内的不同DNA模板,表明瞬时和局部TCDS强烈抑制大肠杆菌中的PgyrA。该结果可以由转录的双超螺旋结构域模型解释,其中在转录RNA聚合酶周围产生(+)和(-)超螺旋结构域。我们还发现,氟喹诺酮类药物如环丙沙星可以在IPTG的存在下,在与不同IPTG诱导型启动子偶联的PgyrA的控制下,大幅提高萤火虫荧光素酶的表达。氟喹诺酮类对PgyrA的刺激也可以通过转录的双超螺旋结构域模型来解释。可以将TCDS的这种独特属性配置为高通量筛选(HTS)分析,以鉴定靶向细菌DNA促旋酶的抗菌化合物。

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