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YtxR Acts as an Overriding Transcriptional Off Switch for the Yersinia enterocolitica Ysc-Yop Type 3 Secretion System

机译:YtxR充当小肠结肠炎耶尔森氏菌Ysc-Yop 3型分泌系统的主要转录关闭开关

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摘要

The Yersinia enterocolitica YtxR protein is a LysR-type transcriptional regulator that induces expression of the ytxAB locus, which encodes a putative ADP-ribosylating toxin. The ytxR and ytxAB genes are not closely linked in the Y. enterocolitica chromosome, and whereas ytxR is present in all sequenced Yersinia spp., the ytxAB locus is not. These observations suggested that there might be other YtxR-regulon members besides ytxAB and prompted us to investigate coregulated genes and gene products by using transcriptional and proteomic approaches. Microarray and reverse transcription-PCR analysis showed that YtxR strongly activates expression of the yts2 locus, which encodes a putative type 2 secretion system, as well as several uncharacterized genes predicted to encode extracytoplasmic proteins. Strikingly, we also discovered that under Ysc-Yop type 3 secretion system-inducing conditions, YtxR prevented the appearance of Yop proteins in the culture supernatant. Microarray and lacZ operon fusion analysis showed that this was due to specific repression of ysc-yop gene expression. YtxR was also able to repress VirF-dependent Φ(yopE-lacZ) and Φ(yopH-lacZ) expression in a strain lacking the virulence plasmid, which suggested a direct repression mechanism. This was supported by DNase I footprinting, which showed that YtxR interacted with the yopE and yopH control regions. Therefore, YtxR is a newly identified regulator of the ysc-yop genes that can act as an overriding off switch for this critical virulence system.
机译:小肠结肠炎耶尔森氏菌YtxR蛋白是一种LysR型转录调节因子,可诱导ytxAB基因座的表达,该基因编码一种假定的ADP-核糖基化毒素。 ytxR和ytxAB基因在小肠结肠炎耶尔森氏菌染色体中没有紧密联系,而ytxR存在于所有测序的耶尔森菌属种中,而ytxAB基因座则不存在。这些观察结果表明除ytxAB以外,可能还有其他YtxR调节子成员,并促使我们使用转录和蛋白质组学方法研究已调控的基因和基因产物。基因芯片和逆转录-PCR分析表明,YtxR强烈激活yts2基因座的表达,该基因编码一个推定的2型分泌系统,以及几个未编码的基因,预计可编码胞浆外蛋白。令人惊讶的是,我们还发现在诱导Ysc-Yop 3型分泌系统的条件下,YtxR阻止了培养上清液中Yop蛋白的出现。芯片和lacZ操纵子融合分析表明,这是由于ysc-yop基因表达的特异性抑制。 YtxR还能够在缺乏毒力质粒的菌株中抑制依赖VirF的Φ(yopE-lacZ)和Φ(yopH-lacZ)表达,这提示了直接的抑制机制。 DNase I足迹证明了这一点,该足迹表明YtxR与yopE和yopH控制区相互作用。因此,YtxR是新发现的 ysc-yop 基因调节剂,可以作为此关键毒力系统的重要开关。

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