Sigma-G RNA polymerase controls forespore-specific expression of the glucose dehydrogenase operon in Bacillus subtilis

Nucleic Acids Res. 1989 Feb 11;17(3):999-1017. doi: 10.1093/nar/17.3.999.

Abstract

The gene encoding glucose dehydrogenase (gdh) is part of an operon whose expression is transcriptionally activated specifically in the developing forespore of Bacillus subtilis at stage III of sporulation. The in vivo startpoint of gdh transcription was determined using primer extension analysis. Deletion mapping and site-specific mutagenesis experiments indicated that the region responsible for regulated expression of gdh in vivo was limited to the "-35" and "-10" regions preceding the transcriptional start site. RNA polymerase containing omega G (E omega G) transcribed gdh in vitro with a start site identical to that found in vivo, and transcription of gdh by E omega G in vitro also did not require any specific sequences upstream from "-35" region. These results suggest that the appearance of E omega G in the forespore at stage III of sporulation is sufficient to cause temporal and compartment-specific expression of the gdh operon.

MeSH terms

  • Bacillus subtilis / enzymology
  • Bacillus subtilis / genetics*
  • Base Sequence
  • Carbohydrate Dehydrogenases / genetics*
  • Chromosome Deletion
  • Cloning, Molecular
  • DNA Mutational Analysis
  • DNA, Ribosomal
  • DNA-Directed RNA Polymerases / physiology*
  • Gene Expression Regulation
  • Glucose Dehydrogenases / genetics*
  • Lac Operon
  • Molecular Sequence Data
  • Nucleotide Mapping
  • Operon*
  • Protein Biosynthesis
  • Sigma Factor / physiology*
  • Spores, Bacterial / enzymology
  • Spores, Bacterial / physiology*
  • Transcription Factors / physiology*

Substances

  • DNA, Ribosomal
  • Sigma Factor
  • Transcription Factors
  • Carbohydrate Dehydrogenases
  • Glucose Dehydrogenases
  • DNA-Directed RNA Polymerases