Müller Stefanie, Pflock Michael, Schär Jennifer, Kennard Simone, Beier Dagmar
Theodor-Boveri-Institut für Biowissenschaften, Lehrstuhl für Mikrobiologie, Universität Würzburg, Am Hubland, D-97074 Würzburg, Germany.
Microbiol Res. 2007;162(1):1-14. doi: 10.1016/j.micres.2006.01.003. Epub 2006 Feb 28.
The human gastric pathogen Helicobacter pylori exhibits a remarkably small repertoire of transcriptional regulators including three complete two-component systems as well as the orphan response regulators HP1021 and HP1043. Both HP1021 and HP1043 show atypical receiver sequences and are required for the normal cell growth of H. pylori. Recently, we demonstrated that phosphorylation of HP1021 and HP1043 according to the two-component paradigm is not a prerequisite for the cell growth-associated functions of these response regulators, raising the question of how the activity of this regulatory proteins is modulated. Here, we report that strict transcriptional control of its expression is not involved in the cell-growth associated function of HP1021. We show that expression of hp1043 is controlled both on the post-transcriptional or post-translational level and by transcriptional regulation. Furthermore, we provide evidence that hp1043 can be replaced by the orthologous gene cj0355 from Campylobacter jejuni.
人类胃部病原体幽门螺杆菌拥有数量极少的转录调节因子,包括三个完整的双组分系统以及孤儿应答调节因子HP1021和HP1043。HP1021和HP1043均显示出非典型的受体序列,并且是幽门螺杆菌正常细胞生长所必需的。最近,我们证明,按照双组分模式对HP1021和HP1043进行磷酸化并非这些应答调节因子细胞生长相关功能的先决条件,这就引出了这些调节蛋白的活性是如何被调控的问题。在此,我们报告,其表达的严格转录控制并不参与HP1021的细胞生长相关功能。我们表明,hp1043的表达在转录后或翻译后水平以及转录调控方面均受到控制。此外,我们提供证据表明,hp1043可以被空肠弯曲菌的直系同源基因cj0355所取代。