首页> 外文期刊>Nucleic acids research >DNA microarray analysis of Bacillus subtilis DegU, ComA and PhoP regulons: an approach to comprehensive analysis of B.subtilis two-component regulatory systems
【24h】

DNA microarray analysis of Bacillus subtilis DegU, ComA and PhoP regulons: an approach to comprehensive analysis of B.subtilis two-component regulatory systems

机译:枯草芽孢杆菌DegU,ComA和PhoP调节剂的DNA微阵列分析:枯草芽孢杆菌两组分调节系统的综合分析方法

获取原文
           

摘要

We have analyzed the regulons of the Bacillus subtilis two-component regulators DegU, ComA and PhoP by using whole genome DNA microarrays. For these experiments we took the strategy that the response regulator genes were cloned downstream of an isopropyl-β-d-thiogalactopyranoside-inducible promoter on a multicopy plasmid and expressed in disruptants of the cognate sensor kinase genes, degS, comP and phoR, respectively. The feasibility of this experimental design to detect target genes was demonstrated by the following two results. First, expression of lacZ fusions of aprE, srfA and ydhF, the target genes of DegU, ComA and PhoP, respectively, was stimulated in their cognate sensor kinase-deficient mutants upon overproduction of the regulators. Secondly, by microarray analysis most of the known target genes for the regulators were detected and, where unknown genes were found, the regulator dependency of several of them was demonstrated. As the mutants used were deficient in the kinase genes, these results show that target candidates can be detected without signal transduction. Using this experimental design, we identified many genes whose dependency on the regulators for expression had not been known. These results suggest the applicability of the strategy to the comprehensive transcription analysis of the B.subtilis two-component systems.
机译:我们已经通过使用全基因组DNA微阵列分析了枯草芽孢杆菌两组分调节剂DegU,ComA和PhoP的调节子。对于这些实验,我们采取了以下策略:将应答调节基因克隆到多拷贝质粒上异丙基-β-d-硫代半乳糖吡喃糖苷诱导型启动子的下游,并分别在同源传感器激酶基因degS,comP和phoR的破坏物中表达。以下两个结果证明了该实验设计检测靶基因的可行性。首先,在过量产生调节剂后,在其同源传感器激酶缺陷型突变体中分别刺激了DegU,ComA和PhoP的靶基因aprE,srfA和ydhF的lacZ融合蛋白的表达。其次,通过微阵列分析,检测到了大多数已知的调控基因靶基因,并且在发现未知基因的地方,证明了其中几个调控基因的依赖性。由于所使用的突变体缺乏激酶基因,因此这些结果表明可以在不进行信号转导的情况下检测到目标候选物。使用该实验设计,我们鉴定了许多未知的表达调控因子基因。这些结果表明该策略可用于枯草芽孢杆菌两组分系统的全面转录分析。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号