Phage N4 RNA polymerase II recruitment to DNA by a single-stranded DNA-binding protein

  1. Richard H. Carter1,2,
  2. Alexander A. Demidenko3,
  3. Susan Hattingh-Willis3, and
  4. Lucia B. Rothman-Denes3,4
  1. 1 Departments of Biochemistry and Molecular Biology, The University of Chicago, Chicago, Illinois 60637, USA
  2. 2 Molecular Genetics and Cell Biology, The University of Chicago, Chicago, Illinois 60637, USA

Abstract

Transcription of bacteriophage N4 middle genes is carried out by a phage-coded, heterodimeric RNA polymerase (N4 RNAPII), which belongs to the family of T7-like RNA polymerases. In contrast to phage T7-RNAP, N4 RNAPII displays no activity on double-stranded templates and low activity on single-stranded templates. In vivo, at least one additional N4-coded protein (p17) is required for N4 middle transcription. We show that N4 ORF2encodes p17 (gp2). Characterization of purified gp2revealed that it is a single-stranded DNA-binding protein that activates N4 RNAPII transcription on single-stranded DNA templates through specific interaction with N4 RNAPII. On the basis of the properties of the proteins involved in N4 RNAPII transcription and of middle promoters, we propose a model for N4 RNAPII promoter recognition, in which gp2plays two roles, stabilization of a single-stranded region at the promoter and recruitment of N4 RNAPII through gp2-N4 RNAPII interactions. Furthermore, we discuss our results in the context of transcription initiation by mitochondrial RNA polymerases.

Keywords

Footnotes

  • Article and publication are at http://www.genesdev.org/cgi/doi/10.1101/gad.1121403.

  • 3 Present address: Dade Behring Inc. Glascow Business Community, Newark, Delaware 19714, USA.

  • 4 Corresponding author. E-MAIL lbrd{at}midway.uchicago.edu; FAX (773) 702-3172.

    • Accepted July 15, 2003.
    • Received June 11, 2003.
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