T-antigen of the human polyomavirus JC attenuates faithful DNA repair by forcing nuclear interaction between IRS-1 and Rad51

J Cell Physiol. 2006 Jan;206(1):35-46. doi: 10.1002/jcp.20425.

Abstract

JC polyomavirus (JCV), which infects 90% of the human population, is detectable in human tumors. Its early protein, JCV T-antigen, transforms cells in vitro and is tumorigenic in experimental animals. Although T-antigen-mediated transformation involves genetic alterations of the affected cells, the mechanism underlying this genomic instability is not known. We show that JCV T-antigen inhibits homologous recombination DNA repair (HRR), which results in an accumulation of mutations. T-antigen does not operate directly but utilizes a cytosolic molecule, insulin receptor substrate 1 (IRS-1). Following T-antigen-mediated nuclear translocation, IRS-1 binds Rad51 at the site of damaged DNA. This T-antigen-mediated inhibition of HRR does not function in cells lacking IRS-1, and can be reproduced in the absence of T-antigen by IRS-1 with artificial nuclear localization signal. Our observations define a new mechanism by which viral protein utilizes cytosolic molecule to inhibit faithful DNA repair, and suggest how polyomaviruses could compromise stability of the genome. (c) 2005 Wiley-Liss, Inc.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Viral, Tumor / metabolism*
  • Base Sequence
  • Cell Nucleus / metabolism*
  • Cells, Cultured
  • DNA Damage
  • DNA Repair*
  • Humans
  • Insulin Receptor Substrate Proteins
  • JC Virus / metabolism*
  • Mice
  • Molecular Sequence Data
  • Mutation
  • Phosphoproteins / metabolism*
  • Rad51 Recombinase / metabolism*
  • Receptor, Insulin / metabolism
  • Recombination, Genetic
  • Sequence Alignment

Substances

  • Antigens, Viral, Tumor
  • IRS1 protein, human
  • Insulin Receptor Substrate Proteins
  • Irs1 protein, mouse
  • Phosphoproteins
  • Receptor, Insulin
  • Rad51 Recombinase