Sze Chun Chau, Bernardo Lisandro M D, Shingler Victoria
Department of Cell and Molecular Biology, Umeå University, S-901 87 Umeå, Sweden.
J Bacteriol. 2002 Feb;184(3):760-70. doi: 10.1128/JB.184.3.760-770.2002.
Pseudomonas-derived regulators DmpR and XylR are structurally and mechanistically related sigma(54)-dependent activators that control transcription of genes involved in catabolism of aromatic compounds. The binding of distinct sets of aromatic effectors to these regulatory proteins results in release of a repressive interdomain interaction and consequently allows the activators to promote transcription from their cognate target promoters. The DmpR-controlled Po promoter region and the XylR-controlled Pu promoter region are also similar, although homology is limited to three discrete DNA signatures for binding sigma(54) RNA polymerase, the integration host factor, and the regulator. These common properties allow cross-regulation of Pu and Po by DmpR and XylR in response to appropriate aromatic effectors. In vivo, transcription of both the DmpR/Po and XylR/Pu regulatory circuits is subject to dominant global regulation, which results in repression of transcription during growth in rich media. Here, we comparatively assess the contribution of (p)ppGpp, the FtsH protease, and a component of an alternative phosphoenolpyruvate-sugar phosphotransferase system, which have been independently implicated in mediating this level of regulation. Further, by exploiting the cross-regulatory abilities of these two circuits, we identify the target component(s) that are intercepted in each case. The results show that (i) contrary to previous speculation, FtsH is not universally required for transcription of sigma(54)-dependent systems; (ii) the two factors found to impact the XylR/Pu regulatory circuit do not intercept the DmpR/Po circuit; and (iii) (p)ppGpp impacts the DmpR/Po system to a greater extent than the XylR/Pu system in both the native Pseudomonas putida and a heterologous Escherichia coli host. The data demonstrate that, despite the similarities of the specific regulatory circuits, the host global regulatory network latches onto and dominates over these specific circuits by exploiting their different properties. The mechanistic implications of how each of the host factors exerts its action are discussed.
源自假单胞菌的调控因子DmpR和XylR是结构和作用机制相关的依赖σ⁵⁴的激活因子,它们控制参与芳香族化合物分解代谢的基因的转录。不同的芳香族效应物与这些调控蛋白的结合会导致抑制性结构域间相互作用的释放,从而使激活因子能够促进其同源靶启动子的转录。DmpR控制的Po启动子区域和XylR控制的Pu启动子区域也相似,尽管同源性仅限于用于结合σ⁵⁴ RNA聚合酶、整合宿主因子和调控因子的三个离散DNA特征。这些共同特性使DmpR和XylR能够响应适当的芳香族效应物对Pu和Po进行交叉调控。在体内,DmpR/Po和XylR/Pu调控回路的转录都受到主要的全局调控,这导致在丰富培养基中生长期间转录受到抑制。在此,我们比较评估了(p)ppGpp、FtsH蛋白酶以及磷酸烯醇丙酮酸-糖磷酸转移酶系统的一个组分的作用,它们已被分别证明参与介导这种调控水平。此外,通过利用这两个回路的交叉调控能力,我们确定了每种情况下被拦截的靶组分。结果表明:(i)与先前的推测相反,FtsH并非依赖σ⁵⁴的系统转录普遍所需;(ii)发现影响XylR/Pu调控回路的两个因子不会拦截DmpR/Po回路;(iii)在天然恶臭假单胞菌和异源大肠杆菌宿主中,(p)ppGpp对DmpR/Po系统的影响比对XylR/Pu系统的影响更大。数据表明,尽管特定调控回路存在相似性,但宿主全局调控网络通过利用它们的不同特性附着并主导这些特定回路。讨论了每个宿主因子发挥作用的机制含义。