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Epoxide-Mediated CifR Repression of cif Gene Expression Utilizes Two Binding Sites in Pseudomonas aeruginosa

机译:环氧化物介导的CIF基因表达的CifR抑制利用铜绿假单胞菌中的两个结合位点。

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摘要

Pseudomonas aeruginosa secretes an epoxide hydrolase virulence factor that reduces the apical membrane expression of ABC transporters such as the cystic fibrosis transmembrane conductance regulator (CFTR). This virulence factor, named CFTR inhibitory factor (Cif), is regulated by a TetR-family, epoxide-responsive repressor known as CifR via direct binding and repression. We identified two sites of CifR binding in the intergenic space between cifR and morB, the first gene in the operon containing the cif gene. We have mapped these binding sites and found they are 27 bp in length, and they overlap the −10 and +1 sites of both the cifR and morB regulatory region and the start of transcription, respectively. In addition, we found that CifR binds to each repression site with differing affinity. Mutagenesis of these binding sites resulted in a loss of DNA binding in vitro, and mutation of one of these sites in vivo resulted in an increase in transcription of both the cif and cifR genes. We characterized cif and cifR gene expression in sputum and found that, whereas cif gene expression varied relative to an in vitro coculture control, cifR gene expression was consistently higher. Analysis of a longitudinal sample of CF isolates from nine patients revealed that Cif protein was expressed over time, although variably, and these changes could not be linked to mutations in the cifR gene or the promoters of these genes. Finally, we tested CifR responsiveness to other epoxides and showed that CifR can respond to multiple epoxides to various degrees.
机译:铜绿假单胞菌分泌一种环氧水解酶毒力因子,该因子可降低ABC转运蛋白(如囊性纤维化跨膜电导调节剂(CFTR))的顶膜表达。这种毒力因子称为CFTR抑制因子(Cif),通过直接结合和阻遏作用,由称为CifR的TetR家族,环氧反应性阻遏物调节。我们在cifR和morB之间的基因间隔中确定了两个CifR结合位点,这是操纵子中第一个包含cif基因的基因。我们已经绘制了这些结合位点的图,发现它们的长度为27 bp,它们分别与cifR和morB调节区的-10和+1位点以及转录起点重叠。此外,我们发现CifR以不同的亲和力与每个阻抑位点结合。这些结合位点的诱变导致体外DNA结合的丧失,而体内这些位点之一的突变导致cif和cifR基因的转录均增加。我们对痰中cif和cifR基因表达进行了表征,发现,尽管cif基因表达相对于体外共培养对照有所不同,但cifR基因表达始终较高。对来自9位患者的CF分离物的纵向样本进行的分析显示,Cif蛋白随时间表达,尽管变化,并且这些变化与cifR基因或这些基因启动子的突变无关。最后,我们测试了CifR对其他环氧化物的响应能力,并表明CifR可以对多种环氧化物做出不同程度的响应。

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