Frederick Jesse R, Rogers Elizabeth A, Marconi Richard T
Department of Microbiology and Immunology, Medical College of Virginia at Virginia Commonwealth University, Richmond, VA 23298-0678, USA.
J Bacteriol. 2008 Sep;190(18):6162-9. doi: 10.1128/JB.00046-08. Epub 2008 Jul 11.
Nothing is currently known regarding the global regulatory networks of Treponema denticola and other oral spirochetes. In this report, we assess the properties and potential phosphotransfer capability of a putative two-component regulatory system (TCS) of T. denticola that is formed by the products of open reading frames tde0032 (a sensor kinase) and tde0033 (a response regulator), henceforth designated AtcS and AtcR, respectively. Using PCR and DNA sequence analyses, atcS and atcR were demonstrated to be widely distributed and conserved among T. denticola isolates. Reverse transcription-PCR (RT-PCR) analyses revealed that these genes are cotranscribed and may also be expressed as part of a larger operon that includes several flanking genes. Analyses using 5' rapid amplification of cDNA ends identified the transcriptional start sites for these operons and provided evidence that some of these genes may be independently transcribed from internal promoters. Real-time RT-PCR and Western blot analysis revealed significant upregulation of atcRS during late-stage growth, indicating growth-phase-dependent expression. Lastly, the phosphorelay capability of the AtcRS system was assessed and demonstrated using recombinant proteins. AtcS was found to undergo autophosphorylation and to transfer phosphate to AtcR. These analyses represent the first description of a functional TCS in an oral spirochetes and provide insight into the transcriptional regulatory mechanisms of these important bacteria.
目前对于齿垢密螺旋体和其他口腔螺旋体的全球调控网络还一无所知。在本报告中,我们评估了齿垢密螺旋体一个假定的双组分调控系统(TCS)的特性和潜在磷酸转移能力,该系统由开放阅读框tde0032(一种传感激酶)和tde0033(一种反应调节因子)的产物形成,此后分别命名为AtcS和AtcR。通过PCR和DNA序列分析,证明atcS和atcR在齿垢密螺旋体分离株中广泛分布且保守。逆转录PCR(RT-PCR)分析表明,这些基因是共转录的,也可能作为一个更大操纵子的一部分表达,该操纵子包括几个侧翼基因。使用5' cDNA末端快速扩增进行的分析确定了这些操纵子的转录起始位点,并提供证据表明其中一些基因可能从内部启动子独立转录。实时RT-PCR和蛋白质印迹分析显示,在生长后期atcRS显著上调,表明其表达依赖于生长阶段。最后,使用重组蛋白评估并证明了AtcRS系统的磷酸传递能力。发现AtcS进行自身磷酸化并将磷酸转移至AtcR。这些分析首次描述了口腔螺旋体中一个功能性的TCS,并为这些重要细菌的转录调控机制提供了见解。