Département de Microbiologie Fondamentale, Université de Lausanne, Bâtiment Biophore, CH-1015 Lausanne, Switzerland.
J Bacteriol. 2011 Jun;193(11):2784-92. doi: 10.1128/JB.00164-11. Epub 2011 Apr 8.
In Pseudomonas aeruginosa, the CbrA/CbrB two-component system is instrumental in the maintenance of the carbon-nitrogen balance and for growth on carbon sources that are energetically less favorable than the preferred dicarboxylate substrates. The CbrA/CbrB system drives the expression of the small RNA CrcZ, which antagonizes the repressing effects of the catabolite repression control protein Crc, an RNA-binding protein. Dicarboxylates appear to cause carbon catabolite repression by inhibiting the activity of the CbrA/CbrB system, resulting in reduced crcZ expression. Here we have identified a conserved palindromic nucleotide sequence that is present in upstream activating sequences (UASs) of promoters under positive control by CbrB and σ(54) RNA polymerase, especially in the UAS of the crcZ promoter. Evidence for recognition of this palindromic sequence by CbrB was obtained in vivo from mutational analysis of the crcZ promoter and in vitro from electrophoretic mobility shift assays using crcZ promoter fragments and purified CbrB protein truncated at the N terminus. Integration host factor (IHF) was required for crcZ expression. CbrB also activated the lipA (lipase) promoter, albeit less effectively, apparently by interacting with a similar but less conserved palindromic sequence in the UAS of lipA. As expected, succinate caused CbrB-dependent catabolite repression of the lipA promoter. Based on these results and previously published data, a consensus CbrB recognition sequence is proposed. This sequence has similarity to the consensus NtrC recognition sequence, which is relevant for nitrogen control.
在铜绿假单胞菌中,CbrA/CbrB 双组分系统在维持碳氮平衡以及在生长碳源方面发挥着重要作用,这些碳源的能量不如首选的二羧酸基质有利。CbrA/CbrB 系统驱动小 RNA CrcZ 的表达,CrcZ 拮抗 RNA 结合蛋白 Crc 的抑制作用。二羧酸似乎通过抑制 CbrA/CbrB 系统的活性引起碳分解代谢物抑制,导致 crcZ 表达减少。在这里,我们鉴定了一个保守的回文核苷酸序列,该序列存在于 CbrB 和 σ(54)RNA 聚合酶正向调控的启动子的上游激活序列 (UAS) 中,特别是在 crcZ 启动子的 UAS 中。通过 crcZ 启动子的突变分析和使用 crcZ 启动子片段和纯化的 N 端截断的 CbrB 蛋白的电泳迁移率变动分析,从体内和体外获得了 CbrB 识别该回文序列的证据。整合宿主因子 (IHF) 是 crcZ 表达所必需的。CbrB 还激活了 lipA(脂肪酶)启动子,但效果不那么明显,显然是通过与 lipA 的 UAS 中的类似但不太保守的回文序列相互作用。正如预期的那样,琥珀酸盐导致 CbrB 依赖的碳分解代谢物抑制 lipA 启动子。基于这些结果和之前发表的数据,提出了一个 CbrB 识别序列的共识。该序列与氮控制相关的 NtrC 识别序列具有相似性。