Countertranscript-driven attenuation system of the pAM beta 1 repE gene

Mol Microbiol. 1996 Jun;20(5):1099-112. doi: 10.1111/j.1365-2958.1996.tb02550.x.

Abstract

The plasmid-encoded RepE protein is absolutely essential and rate-limiting for replication of the promiscuous plasmid pAM beta 1 originating from Enterococcus faecalis. We previously showed that the rep gene is transcribed from a promoter that is negatively regulated (approximately 10-fold reduction) by the CopF repressor. In this report, we show that this transcription is decreased a further approximately 10-times by a countertranscript-driven transcriptional attenuation system. Extensive mutagenesis revealed that this system operates by a mechanism similar to that previously described for the unrelated repC gene of plasmid pT181.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bacterial Proteins / genetics*
  • DNA-Binding Proteins / genetics*
  • Enterococcus faecalis / genetics*
  • Escherichia coli Proteins*
  • Gene Dosage
  • Gene Expression Regulation, Bacterial
  • Mutagenesis
  • Nucleic Acid Conformation
  • Plasmids
  • Promoter Regions, Genetic
  • RNA, Bacterial
  • Repressor Proteins / genetics*
  • Signal Transduction / genetics*
  • Transcription, Genetic*

Substances

  • Bacterial Proteins
  • DNA-Binding Proteins
  • Escherichia coli Proteins
  • RNA, Bacterial
  • RepE protein, E coli
  • Repressor Proteins