Hayashi Kentaro, Kensuke Tsukahara, Kobayashi Kazuo, Ogasawara Naotake, Ogura Mitsuo
Department of Marine Science and Technology, Tokai University, Shizuoka, Japan.
Mol Microbiol. 2006 Mar;59(6):1714-29. doi: 10.1111/j.1365-2958.2006.05059.x.
Rap proteins regulate the activity of response regulators including Spo0F, DegU and ComA. We found that overexpression of either RapG or RapH severely downregulated the expression of srfA, which belongs to the ComA regulon. Disruption of those genes, however, showed small effects on srfA expression. These observations suggested that Bacillus subtilis cells possess a repressor for rapG and rapH. To identify candidate repressors we developed a novel transcription factor array (TF array) assay, in which disruptions of 287 genes encoding regulatory proteins were independently transformed into a strain carrying rapH-lacZ and the resultant transformants were grown on agar plates containing Xgal to detect beta-galactosidase activity. We identified a yvaN disruptant which showed a rapH-overproducing phenotype. DNA microarray analysis of the yvaN mutant suggested that both rapG and rapH were overproduced, leading to inhibition of srfA expression. In a gel retardation assay, purified His-tagged YvaN specifically bound to promoter sequences of rapG and rapH. Further footprint and gel retardation analyses using various deleted probes uncovered critical sequences for YvaN binding. In addition, a lacZ fusion analysis confirmed the significance of YvaN binding for transcription regulation of rapG and rapH. Thus, YvaN was renamed RghR (rapG and rapH repressor). As the rapH gene is activated by ComK and RapH inhibits comK indirectly, this constitutes an autoregulatory loop modulated by RghR.
Rap蛋白调控包括Spo0F、DegU和ComA在内的应答调节因子的活性。我们发现,RapG或RapH的过表达会严重下调属于ComA调控子的srfA的表达。然而,这些基因的缺失对srfA表达的影响较小。这些观察结果表明,枯草芽孢杆菌细胞中存在rapG和rapH的阻遏物。为了鉴定候选阻遏物,我们开发了一种新型转录因子阵列(TF阵列)分析方法,即将编码调控蛋白的287个基因的缺失突变体分别转化到携带rapH - lacZ的菌株中,然后将所得转化体在含有Xgal的琼脂平板上培养,以检测β - 半乳糖苷酶活性。我们鉴定出一个yvaN缺失突变体,其表现出rapH过量产生的表型。对yvaN突变体的DNA微阵列分析表明,rapG和rapH均过量产生,导致srfA表达受到抑制。在凝胶阻滞试验中,纯化的His标签YvaN特异性结合rapG和rapH的启动子序列。使用各种缺失探针进行的进一步足迹分析和凝胶阻滞分析揭示了YvaN结合的关键序列。此外,lacZ融合分析证实了YvaN结合对rapG和rapH转录调控的重要性。因此,YvaN被重新命名为RghR(rapG和rapH阻遏物)。由于rapH基因由ComK激活,而RapH间接抑制comK,这构成了一个由RghR调节的自动调节环。