首页> 美国卫生研究院文献>Journal of Bacteriology >Reexamining Transcriptional Regulation of the Bacillus subtilis htpX Gene and the ykrK Gene Encoding a Novel Type of Transcriptional Regulator and Redefining the YkrK Operator
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Reexamining Transcriptional Regulation of the Bacillus subtilis htpX Gene and the ykrK Gene Encoding a Novel Type of Transcriptional Regulator and Redefining the YkrK Operator

机译:重新检查枯草芽孢杆菌htpX基因和ykrK基因的转录调控编码一种新型的转录调控子并重新定义YkrK算子

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摘要

HtpX is an integral cytoplasmic membrane metalloprotease well conserved in numerous bacteria. A recent study showed that expression of the Bacillus subtilis htpX gene is under dual negative control by Rok and a novel type of transcriptional regulator, YkrK. Here we report that expression of the B. subtilis htpX gene is strongly heat inducible. Contrary to the previous prediction, ykrK expression has been found to be not subject to autoregulation. We have identified the htpX promoter and the authentic ykrK promoter, which is also distinct from the previously predicted one. We have redefined a conserved inverted repeat sequence to be the YkrK operator, which is somewhat different from the previously proposed one. We provide evidence that YkrK is not a substrate of HtpX and that heat induction of htpX is not YkrK mediated. We have also found that the absence of FtsH or HtpX alone did not impair B. subtilis cell viability on LB agar plates at high temperature, whereas the absence of both FtsH and HtpX caused a severe growth defect under heat stress. This finding supports the notion that FtsH and HtpX may have partially overlapping functions in heat resistance. Finally, we show that htpX expression is subject to transient negative control by sigB under heat stress in a Rok- and YkrK-independent manner. Triple negative control of htpX expression at high temperature by rok, sigB, and ykrK may help cells to prevent uncontrolled and detrimental oversynthesis of the HtpX protease.
机译:HtpX是完整的细胞质膜金属蛋白酶,在许多细菌中都非常保守。最近的一项研究表明,枯草芽孢杆菌htpX基因的表达受到Rok和新型转录调节因子YkrK的双重负调控。在这里我们报告枯草芽孢杆菌htpX基因的表达是强烈热诱导的。与先前的预测相反,已发现ykrK表达不受自动调节。我们已经确定了htpX启动子和真正的ykrK启动子,它们也不同于先前预测的启动子。我们将保守的反向重复序列重新定义为YkrK算子,这与先前提出的算子有些不同。我们提供的证据表明YkrK不是HtpX的底物,并且htpX的热诱导不是YkrK介导的。我们还发现,在高温下,单独使用FtsH或HtpX不会损害LB琼脂平板上枯草芽孢杆菌的细胞活力,而同时缺乏FtsH和HtpX会导致热应激下严重的生长缺陷。这一发现支持了FtsH和HtpX在耐热性方面可能部分重叠的观点。最后,我们表明htpX表达受sigB在热应激下以Rok和YkrK独立的方式进行瞬时负调控。 rok,sigB和ykrK在高温下对htpX表达的三重负调控可能有助于细胞防止HtpX蛋白酶不受控制和有害的过度合成。

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