Vaccinia virus uracil DNA glycosylase interacts with the A20 protein to form a heterodimeric processivity factor for the viral DNA polymerase

J Biol Chem. 2006 Feb 10;281(6):3439-51. doi: 10.1074/jbc.M511239200. Epub 2005 Dec 1.

Abstract

The vaccinia virus E9 protein, the catalytic subunit of the DNA polymerase holoenzyme, is inherently distributive under physiological conditions, although infected cells contain a highly processive form of the enzyme. The viral A20 protein was previously characterized as a stoichiometric component of the processivity factor, and an interaction between A20 and E9 was documented in vivo. A20 has been shown to interact with D4, the virally encoded uracil DNA glycosylase (UDG), by yeast-two hybrid and in vitro analysis. Here we confirm that UDG and A20 interact in vivo and show that temperature-sensitive viruses with lesions in the D4R gene show a profound defect in DNA synthesis at the non-permissive temperature. Moreover, cytoplasmic extracts prepared from these infections lack processive polymerase activity in vitro, implicating D4 in the assembly or activity of the processive polymerase. Upon overexpression of 3xFLAG-UDG, A20, and E9 in various combinations, we purified dimeric and trimeric UDG-A20 and UDG-A20-polymerase complexes, respectively. These complexes are stable in 750 mm NaCl and can be further purified by Mono Q chromatography. Notably, the trimeric complex displays robust processive polymerase activity, and the dimeric complex can confer processivity on purified E9. Consistent with previous reports that the catalytic activity of UDG is dispensable for virus replication in tissue culture, we find that the role of UDG role in the polymerase complex is not diminished by mutations targeting residues involved in uracil recognition or excision. Our cumulative data support the conclusion that A20 and UDG form a heterodimeric processivity factor that associates with E9 to comprise the processive polymerase holoenzyme.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Bacteriophage M13 / metabolism
  • Blotting, Southern
  • Catalysis
  • Cell Line
  • Chlorocebus aethiops
  • Chromatography
  • Cytoplasm / metabolism
  • DNA Replication
  • DNA, Viral / metabolism
  • DNA-Directed DNA Polymerase / chemistry*
  • Dimerization
  • Epitopes / chemistry
  • Humans
  • Immunoblotting
  • Immunoprecipitation
  • In Vitro Techniques
  • Mutation
  • Open Reading Frames
  • Phenotype
  • Plasmids / metabolism
  • Protein Binding
  • Protein Biosynthesis
  • Protein Interaction Mapping
  • Silver Staining
  • Software
  • Temperature
  • Transcription, Genetic
  • Uracil / chemistry
  • Uracil-DNA Glycosidase / chemistry*
  • Uracil-DNA Glycosidase / metabolism
  • Vaccinia virus / enzymology*

Substances

  • DNA, Viral
  • Epitopes
  • Uracil
  • DNA-Directed DNA Polymerase
  • Uracil-DNA Glycosidase