Department of Microbiology, Molecular Genetics, and Immunology, University of Kansas Medical Center, 3901 Rainbow Blvd., Kansas City, KS 66160, USA.
J Bacteriol. 2011 Dec;193(23):6605-13. doi: 10.1128/JB.06122-11. Epub 2011 Sep 30.
The TetR family of transcriptional regulators is ubiquitous in bacteria, where it plays an important role in bacterial gene expression. Streptococcus mutans, a gram-positive pathogen considered to be the primary etiological agent in the formation of dental caries, encodes at least 18 TetR regulators. Here we characterized one such TetR regulator, SMU.1349, encoded by the TnSmu2 operon, which appeared to be acquired by the organism via horizontal gene transfer. SMU.1349 is transcribed divergently from the rest of the genes encoded by the operon. By the use of a transcriptional reporter system and semiquantitative reverse transcription-PCR (RT-PCR), we demonstrated that SMU.1349 activates the transcription of several genes that are encoded within the TnSmu2 operon. Gel mobility shift and DNase I footprinting assays with purified SMU.1349 protein demonstrated binding to the intergenic region between SMU.1349 and the TnSmu2 operon; therefore, SMU.1349 is directly involved in gene transcription. Using purified S. mutans RpoD and Escherichia coli RNA polymerase, we also demonstrated in an in vitro transcription assay that SMU.1349 could activate transcription from the TnSmu2 operon promoter. Furthermore, we showed that SMU.1349 could also repress transcription from its own promoter by binding to the intergenic region, suggesting that SMU.1349 acts as both an activator and a repressor. Thus, unlike most of the TetR family proteins, which generally function as transcriptional repressors, SMU.1349 is unique in that it can function as both.
TetR 家族转录调节剂在细菌中无处不在,在细菌基因表达中发挥着重要作用。变形链球菌,一种被认为是龋齿形成的主要病原体的革兰氏阳性菌,至少编码 18 种 TetR 调节剂。在这里,我们对 TnSmu2 操纵子编码的一种 TetR 调节剂 SMU.1349 进行了特征描述,该基因似乎是通过水平基因转移获得的。SMU.1349 与操纵子中其余基因的转录方向相反。通过使用转录报告系统和半定量逆转录-PCR(RT-PCR),我们证明 SMU.1349 激活了 TnSmu2 操纵子内几个基因的转录。用纯化的 SMU.1349 蛋白进行凝胶迁移率变动和 DNA 酶 I 足迹实验表明,SMU.1349 与 SMU.1349 和 TnSmu2 操纵子之间的基因间区结合;因此,SMU.1349 直接参与基因转录。使用纯化的 S. mutans RpoD 和大肠杆菌 RNA 聚合酶,我们还在体外转录实验中证明,SMU.1349 可以激活 TnSmu2 操纵子启动子的转录。此外,我们表明 SMU.1349 也可以通过与基因间区结合来抑制自身启动子的转录,这表明 SMU.1349 既可以作为激活子又可以作为抑制剂。因此,与大多数作为转录抑制剂的 TetR 家族蛋白不同,SMU.1349 是独一无二的,它可以同时作为激活剂和抑制剂。