CbrAB-dependent regulation of pcnB, a poly(A) polymerase gene involved in polyadenylation of RNA in Pseudomonas fluorescens
Article first published online: 7 MAY 2010
© 2010 Society for Applied Microbiology and Blackwell Publishing Ltd
Special Issue: Pseudomonas. Editors: Professors Burkhard Tummler, Victor de Lorenzo, Alain Filloux and Joyce Loper
Volume 12, Issue 6, pages 1674–1683, June 2010
How to Cite
Zhang, X.-X., Liu, Y.-H. and Rainey, P. B. (2010), CbrAB-dependent regulation of pcnB, a poly(A) polymerase gene involved in polyadenylation of RNA in Pseudomonas fluorescens. Environmental Microbiology, 12: 1674–1683. doi: 10.1111/j.1462-2920.2010.02228.x
- Issue published online: 3 JUN 2010
- Article first published online: 7 MAY 2010
- Received 17 December, 2009; accepted 25 February, 2010.
CbrB is a global σ54-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 σ54 promoter in the intergenic region of cbrB and pcnB led to the hypothesis that CbrB regulates pcnB expression in a σ54-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 σ70-like promoter. Deletion of pcnB caused ∼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 σ54 promoter. Genetic analysis showed that the σ54 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.