NZ Institute for Advanced Study, Massey University Auckland, Auckland 0745, New Zealand.
Environ Microbiol. 2010 Jun;12(6):1674-83. doi: 10.1111/j.1462-2920.2010.02228.x. Epub 2010 May 7.
CbrB is a global sigma(54)-dependent regulator required for nutrient acquisition in Pseudomonas. Located downstream of cbrB on the Pseudomonas fluorescens SBW25 chromosome is pcnB, a putative poly(A) polymerase gene. Presence of a sigma(54) promoter in the intergenic region of cbrB and pcnB led to the hypothesis that CbrB regulates pcnB expression in a sigma(54)-dependent manner. Here we show that transcription of pcnB is CbrB dependent. However, 5'-RACE analysis of the pcnB transcript using primers located in the pcnB coding region shows that transcription starts immediately upstream of the putative ATG site at a sigma(70)-like promoter. Deletion of pcnB caused approximately 80% decrease of ployadenylated 23S rRNA; growth of the pcnB mutant was compromised in a range of laboratory media and on sugar beet seedlings. Further 5'-RACE analysis confirmed the existence of the predicted sigma(54) promoter. Genetic analysis showed that the sigma(54) promoter drives expression of crcZ, a homologue of the recently described small RNA from Pseudomonas aeruginosa, in a CbrB-dependent manner. Taken together, our data show that both pcnB and crcZ are part of the CbrB regulon. Moreover, the data draw further attention to the central regulatory role of CbrB and provides a link between mRNA degradation and cellular catabolism.
CbrB 是一种全局性的 sigma(54) 依赖型调控因子,在 Pseudomonas 中负责营养物质的获取。Pseudomonas fluorescens SBW25 染色体上位于 cbrB 下游的是 pcnB,这是一个假定的聚(A)聚合酶基因。cbrB 和 pcnB 之间的基因间隔区存在一个 sigma(54)启动子,这导致了 CbrB 以 sigma(54)依赖的方式调节 pcnB 表达的假设。在这里,我们证明了 pcnB 的转录依赖于 CbrB。然而,使用位于 pcnB 编码区的引物进行的 pcnB 转录的 5'-RACE 分析表明,转录从假定的 ATG 位点的上游开始,使用的是一个类似于 sigma(70)的启动子。pcnB 的缺失导致多聚腺苷酸化的 23S rRNA 减少约 80%;pcnB 突变体在一系列实验室培养基和甜甜菜幼苗上的生长受到影响。进一步的 5'-RACE 分析证实了预测的 sigma(54)启动子的存在。遗传分析表明,sigma(54)启动子以 CbrB 依赖的方式驱动最近在 Pseudomonas aeruginosa 中描述的小 RNA 的同源物 crcZ 的表达。总的来说,我们的数据表明 pcnB 和 crcZ 都是 CbrB 调控子的一部分。此外,这些数据进一步强调了 CbrB 的核心调节作用,并提供了 mRNA 降解和细胞分解代谢之间的联系。