Skip to main navigation Skip to search Skip to main content

Activation of bacterial transcription by distortion of promoter base pairing

Research output: Contribution to journalArticlepeer-review

3 Downloads (Pure)

Abstract

Bacterial RNA polymerase binds and unwinds promoter DNA to initiate transcription. The process is often inefficient and can be stimulated by activator proteins. For example, many activators bind RNA polymerase and promoters simultaneously, stabilizing their interaction. Working with the multiple antibiotic resistance activator (MarA) protein of Escherichia coli, we have discovered an alternative mechanism. We show that, when bound upstream of the flgBCDEFGHIJ/KL operon, MarA perturbs base pairing adjacent to its DNA target. This compensates for inefficient duplex unwinding by RNA polymerase and, as a result, activates transcription. Consistent with our model, an appropriate base pair mismatch mimics the effect of, and removes the need for, MarA. As many regulators alter DNA conformation, we suggest that this mechanism of activation could be commonplace.

Original languageEnglish
Article numbergkaf1424
Number of pages14
JournalNucleic Acids Research
Volume54
Issue number1
Early online date8 Jan 2026
DOIs
Publication statusPublished - 13 Jan 2026

Keywords

  • Promoter Regions, Genetic
  • Base Pairing
  • Escherichia coli/genetics
  • Escherichia coli Proteins/metabolism
  • DNA-Directed RNA Polymerases/metabolism
  • DNA-Binding Proteins/metabolism
  • DNA, Bacterial/chemistry
  • Gene Expression Regulation, Bacterial
  • Transcription, Genetic
  • Operon
  • Transcriptional Activation

Fingerprint

Dive into the research topics of 'Activation of bacterial transcription by distortion of promoter base pairing'. Together they form a unique fingerprint.

Cite this