National Key Laboratory of Agricultural Microbiology, Center for Proteomics Research, College of Life Science and Technology, Huazhong Agricultural University, Wuhan, China.
Biochem Biophys Res Commun. 2011 Aug 12;411(4):726-31. doi: 10.1016/j.bbrc.2011.07.014. Epub 2011 Jul 18.
Transcriptional regulation plays a critical role during the infection of Mycobacterium tuberculosis, the causative agent of tuberculosis. A two-component system, PhoPR, is clearly involved in the regulation of pathogenic virulence and persistence. However, the regulatory mechanism, as well as the regulator, of the phoPR operon remains uncharacterized in M. tuberculosis and its related species thus far. In the present study, we characterize an ArsR transcriptional factor, corresponding to Rv2034 and Ms6762 in M. tuberculosis and Mycobacterium smegmatis, respectively, as the first regulator of phoP in both mycobacterial species. The interaction between ArsR regulator and target promoters is conserved in these two mycobacterial species, and an inverted repeat sequence motif is successfully mapped out for the recognition of ArsR. Utilizing lacZ reporter genes and overexpression analysis, the ArsR regulator is shown to positively regulate the expression of phoP in M. smegmatis, different from most ArsR family regulators generally as a repressor. The current study establishes a direct link between the ArsR transcriptional factor and the regulation of phoP in mycobacteria. Our findings imply that ArsR may be involved in the pathogenesis of M. tuberculosis through its regulation of the phoPR operon.
转录调控在结核分枝杆菌(导致结核病的病原体)感染过程中起着至关重要的作用。双组分系统 PhoPR 显然参与了致病毒力和持久性的调节。然而,迄今为止,结核分枝杆菌及其相关物种中 phoPR 操纵子的调节机制以及调节剂仍未被阐明。在本研究中,我们将 ArsR 转录因子(对应于结核分枝杆菌和耻垢分枝杆菌中的 Rv2034 和 Ms6762)鉴定为这两种分枝杆菌中 phoP 的第一个调节剂。在这两种分枝杆菌中,ArsR 调节剂与靶启动子之间的相互作用是保守的,并且成功映射出了用于 ArsR 识别的反向重复序列基序。利用 lacZ 报告基因和过表达分析表明,ArsR 调节剂在耻垢分枝杆菌中正向调节 phoP 的表达,与大多数 ArsR 家族调节剂通常作为抑制剂不同。本研究在分枝杆菌中建立了 ArsR 转录因子和 phoP 调节之间的直接联系。我们的研究结果表明,ArsR 可能通过调节 phoPR 操纵子参与结核分枝杆菌的发病机制。