Conversion of the ω subunit of Escherichia coli RNA polymerase into a transcriptional activator or an activation target

  1. Simon L. Dove and
  2. Ann Hochschild
  1. Department of Microbiology and Molecular Genetics, Harvard Medical School, Boston, Massachusetts 02115 USA

Abstract

Evidence obtained in both eukaryotes and prokaryotes indicates that arbitrary contacts between DNA-bound proteins and components of the transcriptional machinery can activate transcription. Here we demonstrate that the Escherichia coli ω protein, which copurifies with RNA polymerase, can function as a transcriptional activator when linked covalently to a DNA-binding protein. We show further that ω can function as an activation target when this covalent linkage is replaced by a pair of interacting polypeptides fused to the DNA-binding protein and to ω, respectively. Our findings imply that the ω protein is associated with RNA polymerase holoenzyme in vivo, and provide support for the hypothesis that contact between a DNA-bound protein and any component of E. coli RNA polymerase can activate transcription.

Keywords

Footnotes

  • Corresponding author.

  • E-MAIL ahochsch{at}warren.med.harvard.edu; FAX (617) 738-7664.

    • Received December 3, 1997.
    • Accepted January 15, 1998.
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