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首页> 外文期刊>BMC Microbiology >Architecture of divergent flagellar promoters controlled by CtrA in Rhodobacter sphaeroides
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Architecture of divergent flagellar promoters controlled by CtrA in Rhodobacter sphaeroides

机译:CtrA控制的球形红球菌中不同鞭毛启动子的结构

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Rhodobacter sphaeroides has two sets of flagellar genes, fla1 and fla2, that are responsible for the synthesis of two different flagellar structures. The expression of the fla2 genes is under control of CtrA. In several α-proteobacteria CtrA is also required for the expression of the flagellar genes, but the architecture of CtrA-dependent promoters has only been studied in detail in Caulobacter crescentus. In many cases the expression of fla genes originates from divergent promoters located a few base pairs apart, suggesting a particular arrangement of the cis-acting sites. Here we characterized several control regions of the R. sphaeroides fla2 genes and analyzed in detail two regions containing the divergent promoters flgB2p-fliI2p, and fliL2p-fliF2p. Binding sites for CtrA of these promoters were identified in silico and tested by site directed mutagenesis. We conclude that each one of these promoter regions has a particular arrangement, either a single CtrA binding site for activation of fliL2p and fliF2p, or two independent sites for activation of flgB2p and fliI2p. ChIP experiments confirmed that CtrA binds to the control region containing the flgB2 and fliI2 promoters, supporting the notion that CtrA directly controls the expression of the fla2 genes. The flgB and fliI genes are syntenic and show a short intercistronic region in closely related bacterial species. We analyzed these regions and found that the arrangement of the CtrA binding sites varies considerably. The results in this work reveal the arrangement of the fla2 divergent promoters showing that CtrA promotes transcriptional activation using more than a single architecture.
机译:球形球形红细菌具有两组鞭毛基因fla1和fla2,它们负责合成两个不同的鞭毛结构。 fla2基因的表达受CtrA的控制。在几种α-变形杆菌中,鞭毛基因的表达也需要CtrA,但是CtrA依赖性启动子的结构仅在新月形杆菌中进行了详细研究。在许多情况下,fla基因的表达源自相距数个碱基对的不同启动子,这表明顺式作用位点的特定排列。在这里,我们表征了球形红球菌fla2基因的几个控制区,并详细分析了两个包含趋异启动子flgB2p-fliI2p和fliL2p-fliF2p的区域。在计算机上鉴定了这些启动子的CtrA结合位点,并通过位点定向诱变进行了测试。我们得出的结论是,这些启动子区域中的每个区域都有特定的排列方式,或者是用于激活fliL2p和fliF2p的单个CtrA结合位点,或者是用于激活flgB2p和fliI2p的两个独立位点。 ChIP实验证实CtrA与包含flgB2和fliI2启动子的控制区结合,支持CtrA直接控制fla2基因表达的观点。 flgB和fliI基因是同系的,在紧密相关的细菌物种中显示出较短的顺反子区域。我们分析了这些区域,发现CtrA结合位点的排列差异很大。这项工作的结果揭示了fla2趋异性启动子的排列,表明CtrA使用一种以上的结构来促进转录激活。

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