Escherichia coli DNA polymerase III holoenzyme subunits alpha, beta, and gamma directly contact the primer-template

J Biol Chem. 1995 Mar 10;270(10):5606-13. doi: 10.1074/jbc.270.10.5606.

Abstract

Escherichia coli DNA polymerase III holoenzyme forms a stable initiation complex with RNA-primed template in the presence of ATP. To determine the linear arrangement of the holoenzyme subunits along the primer-template duplex region, we cross-linked holoenzyme to a series of photo-reactive primers. Site-specific photo-cross-linking revealed that the alpha, beta, and gamma subunits formed ATP-dependent contacts with the primer-template. The alpha-polymerase catalytic subunit covalently attached to nucleotide positions -3, -9, and -13 upstream of the primer terminus, with the most efficient adduct formation occurring at position -9. The gamma subunit contacted the primer at positions -13, -18, and -22, with the strongest gamma-primer interactions occurring at position -18. The beta subunit predominated in cross-linking at position -22. Thus, within the initiation complex, alpha contacts roughly the first 13 nucleotides upstream of the 3'-primer terminus followed by gamma at -18 and beta at -22, and the gamma subunit remains a part of the initiation complex, bridging the alpha and beta subunits. Analyses of the interaction of photo-activatible primer-templates with the preinitiation complex proteins (gamma-complex (gamma-delta-delta'-chi-psi) and beta subunit) revealed the gamma subunit within the preinitiation complex covalently attached to primer at position -3. However, addition of core DNA polymerase III to preinitiation complex, fully reconstituting holoenzyme resulted in replacement of gamma by alpha at the primer terminus. These data indicate that assembly of holoenzyme onto a primer-template can occur in distinct stages and results in a structural rearrangement during initiation complex formation.

Publication types

  • Comparative Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Base Sequence
  • DNA Adducts / analysis
  • DNA Polymerase III / chemistry*
  • DNA Polymerase III / metabolism*
  • DNA Primers / chemical synthesis
  • DNA Primers / metabolism*
  • Escherichia coli / enzymology*
  • Indicators and Reagents
  • Macromolecular Substances
  • Molecular Sequence Data
  • Oligonucleotide Probes
  • Protein Binding
  • Templates, Genetic

Substances

  • DNA Adducts
  • DNA Primers
  • Indicators and Reagents
  • Macromolecular Substances
  • Oligonucleotide Probes
  • Adenosine Triphosphate
  • DNA Polymerase III