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SwrA 通过与 DegU N 端结构域相互作用调控枯草芽孢杆菌 DegU 的组装。

SwrA regulates assembly of Bacillus subtilis DegU via its interaction with N-terminal domain of DegU.

机构信息

Institute of Oceanic Research and Development, Tokai University, Shizuoka, Japan.

出版信息

J Biochem. 2012 Jun;151(6):643-55. doi: 10.1093/jb/mvs036. Epub 2012 Apr 9.

Abstract

The Bacillus subtilis response regulator DegU controls many physiological events including swarming motility and exoprotease production. Swarming motility is a multicellular movement of hyper-flagellated cells on a surface. The swarming motility regulator SwrA and DegU cooperatively drive transcription of fla/che encoding flagella components, chemotaxis constituents and motility-specific sigma factor, which is regarded as the primary event in the development of motility. We have identified ycdA involved in swarming motility, encoding a putative lipoprotein. We showed that the ycdA gene is positively regulated by DegU and SwrA. Mutational analysis of ycdA-lacZ revealed that SwrA changes the use of cis-acting sites for DegU. This suggested that SwrA operates the DegU-regulation mode through changes in the DegU assembly state. DegU binding to the ycdA-promoter region carrying an unusual arrangement of DegU-recognition sequences with low affinity was found to be stimulated by SwrA in electrophoretic mobility shift assay and DNase I footprinting. Yeast two- and three-hybrid analyses revealed that the N-terminal domain of DegU interacts with whole DegU, which is facilitated by SwrA. Together, these results demonstrate that SwrA can stabilize the binding of DegU to the ycdA promoter with low affinity. Thus, SwrA is a novel type of bacterial transcription factor in this regard.

摘要

枯草芽孢杆菌反应调节剂 DegU 控制着许多生理事件,包括群集运动和外蛋白酶的产生。群集运动是一种超鞭毛细胞在表面上的多细胞运动。群集运动调节剂 SwrA 和 DegU 协同驱动编码鞭毛成分、趋化作用成分和运动特异性 σ 因子的 fla/che 的转录,这被认为是运动发展的主要事件。我们已经确定了参与群集运动的 ycdA,其编码一个假定的脂蛋白。我们表明,ycdA 基因受 DegU 和 SwrA 的正调控。ycdA-lacZ 的突变分析表明,SwrA 改变了 DegU 的顺式作用位点的使用。这表明 SwrA 通过改变 DegU 的组装状态来操作 DegU 调节模式。在凝胶电泳迁移率变动分析和 DNase I 足迹法中发现,SwrA 刺激 DegU 与携带低亲和力 DegU 识别序列的不寻常排列的 ycdA 启动子区域的结合。酵母双杂交和三杂交分析表明,DegU 的 N 端结构域与整个 DegU 相互作用,这是由 SwrA 促进的。总之,这些结果表明 SwrA 可以稳定 DegU 与 ycdA 启动子的低亲和力结合。因此,SwrA 在这方面是一种新型的细菌转录因子。

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