Suppr超能文献

质粒pB171双par位点中的调控相互作用。

Regulatory cross-talk in the double par locus of plasmid pB171.

作者信息

Ringgaard Simon, Ebersbach Gitte, Borch Jonas, Gerdes Kenn

机构信息

Department of Biochemistry and Molecular Biology, Campusvej 55, University of Southern Denmark, DK-5230 Odense M, Denmark.

出版信息

J Biol Chem. 2007 Feb 2;282(5):3134-45. doi: 10.1074/jbc.M609092200. Epub 2006 Nov 8.

Abstract

The double par locus of Escherichia coli virulence factor pB171 consists of two adjacent and oppositely oriented par loci of different types, called par1 and par2. par1 encodes an actin ATPase (ParM), and par2 encodes an oscillating, MinD-like ATPase (ParA). The par loci share a central cis-acting region of approximately 200 bp, called parC1, located between the two par loci. An additional cis-acting region, parC2, is located downstream of the parAB operon of par2. Here we show that ParR of par1 and ParB of par2 bind cooperatively to unrelated sets of direct repeats in parC1 to form the cognate partition and promoter repression complexes. Surprisingly, ParB repressed transcription of the noncognate par operon, indicating cross-talk and possibly epistasis between the two systems. The par promoters, P1 and P2, affected each other negatively. The DNA binding activities of ParR and ParB correlated well with the observed transcriptional regulation of the par operons in vivo and in vitro. Integration host factor (IHF) was identified as a novel factor involved in par2-mediated plasmid partitioning.

摘要

大肠杆菌毒力因子pB171的双par位点由两个相邻且方向相反的不同类型的par位点组成,分别称为par1和par2。par1编码一种肌动蛋白ATP酶(ParM),par2编码一种振荡的、类似MinD的ATP酶(ParA)。这两个par位点共享一个位于它们之间的约200 bp的中央顺式作用区域,称为parC1。另一个顺式作用区域parC2位于par2的parAB操纵子下游。在此我们表明,par1的ParR和par2的ParB协同结合到parC1中不相关的直接重复序列组上,形成同源分配和启动子抑制复合物。令人惊讶的是,ParB抑制了非同源par操纵子的转录,表明这两个系统之间存在串扰以及可能的上位性。par启动子P1和P2相互产生负向影响。ParR和ParB的DNA结合活性与体内和体外观察到的par操纵子的转录调控密切相关。整合宿主因子(IHF)被鉴定为参与par2介导的质粒分配的一个新因子。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验