PARP-1 interaction with VP1 capsid protein regulates polyomavirus early gene expression

J Mol Biol. 2006 Nov 3;363(4):773-85. doi: 10.1016/j.jmb.2006.05.077. Epub 2006 Jun 30.

Abstract

Poly(ADP-ribose)polymerases are involved in fundamental cellular events as well as they seem to be associated to some viral infection process. In this work, the poly(ADP-ribose)polymerase-1 (PARP-1) role in the polyomavirus life cycle has been investigated. Early viral transcription was reduced by competitive inhibitors of PARPs in Swiss 3T3 cells and almost abolished in PARP-1 knockout fibroblasts and in wild-type fibroblasts when PARP-1 was silenced by RNA interference. In vivo chromatin immunoprecipitation assays showed that poly(ADP-ribosyl)ation (poly(ADP-ribose)) facilitates the release of the capsid protein viral protein 1 (VP1) from the chromatin of infecting virions. In vitro experiments demonstrated that VP1 stimulates the enzymatic activity of PARP-1 and binds non-covalently both protein-free and PARP-1-bound poly(ADP-ribose). Our studies suggest that PARP-1 promotes the complete VP1 displacement from viral DNA favouring the viral early transcription.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3 Cells
  • Animals
  • Capsid / metabolism
  • Capsid Proteins / metabolism*
  • Gene Expression Regulation, Viral*
  • Genes, Immediate-Early / genetics*
  • Mice
  • Models, Genetic
  • Poly (ADP-Ribose) Polymerase-1
  • Poly Adenosine Diphosphate Ribose / metabolism
  • Poly(ADP-ribose) Polymerases / metabolism*
  • Polyomavirus / genetics*
  • Polyomavirus / pathogenicity
  • Protein Binding
  • Transcription, Genetic
  • Virus Internalization

Substances

  • Capsid Proteins
  • VP1 protein, polyomavirus
  • Poly Adenosine Diphosphate Ribose
  • Parp1 protein, mouse
  • Poly (ADP-Ribose) Polymerase-1
  • Poly(ADP-ribose) Polymerases