Cyclic AMP Receptor Protein Regulates cspD, a Bacterial Toxin Gene, in Escherichia coli

• Published in: Journal of bacteriology 2014-04, Vol.196 (8), p.1569-1577
• Main Authors: Uppal, Sheetal, Shetty, Deeksha M, Jawali, Narendra
• Format: Article
• Language: English
• Subjects: bacterial toxins; Bacterial Toxins - biosynthesis; Bacteriology; Binding Sites; cold stress; cyclic AMP; DNA replication; DNA, Bacterial - metabolism; DNA-Binding Proteins - metabolism; DNA-directed RNA polymerase; E coli; Electrophoretic Mobility Shift Assay; Escherichia coli; Escherichia coli - genetics; Escherichia coli - metabolism; Escherichia coli Proteins - genetics; Escherichia coli Proteins - metabolism; gel electrophoresis; Gene expression; gene expression regulation; Gene Expression Regulation, Bacterial; genes; Heat-Shock Proteins - genetics; mutation; Protein Binding; Protein expression; Receptors, Cyclic AMP - metabolism; Regulatory Elements, Transcriptional; sequence analysis; toxicity; transcription (genetics); Transcription factors; Transcription, Genetic
• ISSN: 0021-9193; 1098-5530
• DOI: 10.1128/JB.01476-13

cspD, a member of cspA family of cold shock genes in Escherichia coli, is not induced during cold shock. Its expression is induced during stationary phase. CspD inhibits DNA replication, and a high level of the protein is toxic to cells. Recently, CspD was proposed to be associated with persister cell formation in E. coli. Here, we show that cyclic AMP receptor protein (CRP) upregulates cspD transcription. Sequence analysis of the cspD upstream region revealed two tandem CRP target sites, CRP site-I (the proximal site centered at −83.5 with respect to the transcription start) and CRP site-II (the distal site centered at −112.5). The results from electrophoretic mobility shift assays showed that CRP indeed binds to these two target sites in PcspD. The promoter-proximal CRP target site was found to play a major role in PcspD activation by CRP, as studied by transcriptional fusions carrying mutations in the target sites. The results from in vitro transcription assays demonstrated that CRP activates PcspD transcription in the absence of additional factors other than RNA polymerase. The requirement for activating region 1 of CRP in PcspD activation, along with the involvement of the 287, 265, and 261 determinants of the α-CTD, suggest that CRP activates by a class I-type mechanism. However, only moderate activation in vitro was observed compared to high activation in vivo, suggesting there might be additional activators of PcspD. Overall, our findings show that CRP, a global metabolic regulator in E. coli, activates a gene potentially related to persistence.