Transcription activation at Class II CRP-dependent promoters: the role of different activating regions

• Published in: Nucleic acids research 1997-01, Vol.25 (2), p.326-332
• Main Authors: Rhodius, Virgil A., West, David M., Webster, Christine L., Busby, Stephen J. W., Savery, Nigel J.
• Format: Article
• Language: English
• Subjects: Base Sequence; Binding Sites - genetics; Carrier Proteins; Cloning, Molecular; Cyclic AMP Receptor Protein - metabolism; Cyclic AMP Receptor Protein - pharmacology; DNA-Directed RNA Polymerases - chemistry; DNA-Directed RNA Polymerases - metabolism; Escherichia coli; Escherichia coli - chemistry; Escherichia coli - metabolism; Kinetics; Molecular Sequence Data; Promoter Regions, Genetic - genetics; Protein Binding; RNA-Binding Proteins - genetics; RNA-Binding Proteins - metabolism; Transcriptional Activation - genetics
• ISSN: 0305-1048; 1362-4962; 1362-4962
• DOI: 10.1093/nar/25.2.326

Transcription activation by the Escherichia coli cyclic AMP receptor protein (CRP) at Class II promoters is dependent on direct interactions between two surface-exposed activating regions (AR1 and AR2) and two contact sites in RNA polymerase. The effects on transcription activation of disrupting either AR1 or AR2 have been measured at different Class II promoters. AR2 but not AR1 is essential for activation at all the Class II promoters that were tested. The effects of single positive control substitutions in AR1 and AR2 vary from one promoter to another: the effects of the different substitutions are contingent on the −35 hexamer sequence. Abortive initiation assays have been used to quantify the effects of positive control substitutions in each activating region on the kinetics of transcription initiation at the Class II CRP-dependent promoter pmelRcon. At this promoter, the HL159 substitution in AR1 results in a defect in the initial binding of RNA polymerase whilst the KE101 substitution in AR2 reduces the rate of isomerization from the closed to the open complex.