Identifying interacting regions in the beta subunit of Escherichia coli RNA polymerase

J Mol Biol. 1996 May 3;258(2):213-23. doi: 10.1006/jmbi.1996.0244.

Abstract

Numerous physical and genetic approaches have identified residues in the alpha, beta, beta' and sigma subunits of Escherichia coli RNA polymerase that are involved in transcriptional processes; in contrast, relatively little data exist to demonstrate interacting regions within or between the subunits themselves. As a means of identifying regions in the beta subunit that may interact, we have sought intragenic suppressor mutations of a class of elongation-defective and termination-proficient inviable rpoB alleles that affect highly conserved residues. We obtained intragenic allele-specific suppressors of GD566 (located in conserved region D) and AV676 (located in conserved region E). With one exception, these allele-specific suppressors also map to highly conserved regions of the beta subunit. Allele specific suppression is a genetic criterion for protein-protein interaction. Moreover, the functional properties of the mutants suggests that suppression is likely to result from protein-protein interaction rather than from functional compensation. Our suppression studies provide evidence for the interaction of conserved regions B and D as well as conserved regions E and H of the beta polypeptide. We suggest that these, as well as other conserved regions of the beta polypeptide, may interact with each other to provide a framework for the function of the enzyme.

MeSH terms

  • Alleles
  • Amino Acid Sequence
  • Base Sequence
  • Binding Sites
  • Chromosome Mapping
  • Conserved Sequence
  • DNA, Bacterial
  • DNA-Directed RNA Polymerases / genetics
  • DNA-Directed RNA Polymerases / metabolism*
  • Escherichia coli / enzymology*
  • Escherichia coli / genetics
  • Humans
  • Molecular Sequence Data
  • Suppression, Genetic
  • Transcription, Genetic

Substances

  • DNA, Bacterial
  • DNA-Directed RNA Polymerases