Functional analysis of the heat shock regulator HrcA of Chlamydia trachomatis

J Bacteriol. 2002 Dec;184(23):6566-71. doi: 10.1128/JB.184.23.6566-6571.2002.

Abstract

HrcA is a regulator of bacterial heat shock gene expression that binds to a cis-acting DNA element called CIRCE. It has been proposed that HrcA and CIRCE function as a repressor-operator pair. We have purified recombinant HrcA from the pathogenic bacterium Chlamydia trachomatis and have shown that it is a DNA-binding protein that functions as a negative regulator of transcription. HrcA bound specifically to the CIRCE element in a concentration-dependent manner. HrcA repressed the in vitro transcription of a chlamydial heat shock promoter, and this repression was promoter specific. HrcA-mediated repression appears to be dependent on the topological state of the promoter, as repression on a supercoiled promoter template was greater than that on a linearized template. These results provide direct support for the role of HrcA as a transcriptional repressor in bacteria. This is the first report of the in vitro reconstitution of transcriptional regulation in Chlamydia.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Base Sequence
  • Chlamydia trachomatis / genetics
  • Chlamydia trachomatis / metabolism*
  • Chlamydia trachomatis / physiology
  • DNA-Binding Proteins
  • Enhancer Elements, Genetic / genetics
  • Enhancer Elements, Genetic / physiology*
  • Escherichia coli Proteins*
  • Gene Expression Regulation, Bacterial*
  • HSP70 Heat-Shock Proteins / genetics
  • HSP70 Heat-Shock Proteins / metabolism
  • Heat-Shock Response*
  • Molecular Sequence Data
  • Promoter Regions, Genetic
  • Repressor Proteins / genetics
  • Repressor Proteins / metabolism*
  • Transcription, Genetic*

Substances

  • Bacterial Proteins
  • DNA-Binding Proteins
  • Escherichia coli Proteins
  • HSP70 Heat-Shock Proteins
  • Repressor Proteins
  • dnaK protein, E coli