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反义核酶抑制DNA促旋酶对大肠杆菌rec A的影响。

Impact of DNA gyrase inhibition by antisense ribozymes on rec A in E. coli.

作者信息

Shilpakala Sainath Rao, Raghunathan Malathi

机构信息

Department of Genetics, Dr ALMPG Institute of Basic Medical Sciences, University of Madras, Taramani Campus, Chennai, India.

出版信息

Mol Biol Rep. 2009 Sep;36(7):1937-42. doi: 10.1007/s11033-008-9402-5. Epub 2008 Nov 4.

Abstract

The chromosome of E. coli is maintained in a negatively supercoiled state, and supercoiling levels are affected by growth phase and a variety of environmental stimuli. Regulation of DNA supercoiling yields a complex spectrum of effects on the E. coli recA system. Previous studies indicated that inhibition of DNA gyrase by antibiotics that act on the DNA gyrase A subunit results in turning on the recA system. Here we show that antisense ribozymes that act on the DNA gyrase A subunit can also induce recA. We used real time PCR and immunoblot to analyze the impact of DNA gyrase A inhibition by antisense ribozymes on recA expression. When gyrase A was inhibited by the RNase P mediated antisense ribozymes the expression of recA was induced around 130-fold as seen by real time PCR analysis. This suggests that repair pathway is induced by antisense ribozymes against DNA gyrase A and the damage produced by these ribozymes may be similar to that produced by fluoroquinolones.

摘要

大肠杆菌的染色体维持在负超螺旋状态,超螺旋水平受生长阶段和多种环境刺激的影响。DNA超螺旋的调节对大肠杆菌recA系统产生一系列复杂的影响。先前的研究表明,作用于DNA促旋酶A亚基的抗生素对DNA促旋酶的抑制会导致recA系统开启。在此我们表明,作用于DNA促旋酶A亚基的反义核酶也能诱导recA。我们使用实时PCR和免疫印迹来分析反义核酶对DNA促旋酶A的抑制对recA表达的影响。当促旋酶A被RNase P介导的反义核酶抑制时,通过实时PCR分析可见recA的表达被诱导了约130倍。这表明针对DNA促旋酶A的反义核酶可诱导修复途径,并且这些核酶产生的损伤可能与氟喹诺酮类药物产生的损伤相似。

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