Charity James C, Costante-Hamm Michelle M, Balon Emmy L, Boyd Dana H, Rubin Eric J, Dove Simon L
Division of Infectious Diseases, Children's Hospital, Harvard Medical School, Boston, Massachusetts, United States of America.
PLoS Pathog. 2007 Jun;3(6):e84. doi: 10.1371/journal.ppat.0030084.
The MglA protein is the only known regulator of virulence gene expression in Francisella tularensis, yet it is unclear how it functions. F. tularensis also contains an MglA-like protein called SspA. Here, we show that MglA and SspA cooperate with one another to control virulence gene expression in F. tularensis. Using a directed proteomic approach, we show that both MglA and SspA associate with RNA polymerase (RNAP) in F. tularensis, and that SspA is required for MglA to associate with RNAP. Furthermore, bacterial two-hybrid and biochemical assays indicate that MglA and SspA interact with one another directly. Finally, through genome-wide expression analyses, we demonstrate that MglA and SspA regulate the same set of genes. Our results suggest that a complex involving both MglA and SspA associates with RNAP to positively control virulence gene expression in F. tularensis. The F. tularensis genome is unusual in that it contains two genes encoding different alpha subunits of RNAP, and we show here that these two alpha subunits are incorporated into RNAP. Thus, as well as identifying SspA as a second critical regulator of virulence gene expression in F. tularensis, our findings provide a framework for understanding the mechanistic basis for virulence gene control in a bacterium whose transcription apparatus is unique.
MglA蛋白是已知的唯一调控土拉弗朗西斯菌毒力基因表达的调节因子,但其作用机制尚不清楚。土拉弗朗西斯菌还含有一种名为SspA的类MglA蛋白。在此,我们表明MglA和SspA相互协作以控制土拉弗朗西斯菌的毒力基因表达。使用定向蛋白质组学方法,我们发现MglA和SspA在土拉弗朗西斯菌中均与RNA聚合酶(RNAP)相关联,并且SspA是MglA与RNAP相关联所必需的。此外,细菌双杂交和生化分析表明MglA和SspA直接相互作用。最后,通过全基因组表达分析,我们证明MglA和SspA调控同一组基因。我们的结果表明,一个包含MglA和SspA的复合物与RNAP相关联,以正向控制土拉弗朗西斯菌的毒力基因表达。土拉弗朗西斯菌的基因组不同寻常之处在于它包含两个编码RNAP不同α亚基的基因,我们在此表明这两个α亚基被整合到RNAP中。因此,除了将SspA鉴定为土拉弗朗西斯菌中毒力基因表达的第二个关键调节因子外,我们的发现还为理解一种转录装置独特的细菌中毒力基因控制的机制基础提供了一个框架。