Architectural requirements for optimal activation by tandem CRP molecules at a class I CRP-dependent promoter

FEMS Microbiol Lett. 2002 Apr 23;210(1):55-60. doi: 10.1111/j.1574-6968.2002.tb11159.x.

Abstract

The Escherichia coli cyclic AMP receptor protein (CRP) activates transcription at target promoters by interacting with the C-terminal domain of the RNA polymerase alpha subunit. We have constructed a set of promoters carrying tandem DNA sites for CRP with one site centred at position -61.5 and the other site located at different upstream positions. Optimal CRP-dependent activation of transcription is observed when the upstream DNA site for CRP is located at position -93.5 or at position -103.5. Evidence is presented to suggest that activation by the upstream-bound CRP molecule is due to interaction with the C-terminal domain of the RNA polymerase alpha subunit.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / metabolism*
  • Base Sequence
  • Carrier Proteins
  • Cyclic AMP / metabolism
  • Cyclic AMP Receptor Protein / chemistry
  • Cyclic AMP Receptor Protein / genetics*
  • Cyclic AMP Receptor Protein / metabolism*
  • DNA-Directed RNA Polymerases / metabolism
  • Molecular Sequence Data
  • Promoter Regions, Genetic*
  • Protein Subunits
  • Sequence Alignment
  • Sequence Homology, Nucleic Acid

Substances

  • Bacterial Proteins
  • Carrier Proteins
  • Cyclic AMP Receptor Protein
  • Protein Subunits
  • Cyclic AMP
  • DNA-Directed RNA Polymerases