HPV 5 and 8 E6 expression reduces ATM protein levels and attenuates LINE-1 retrotransposition

Virology. 2013 Aug 15;443(1):69-79. doi: 10.1016/j.virol.2013.04.022. Epub 2013 May 23.

Abstract

The expression of the E6 protein from certain members of the HPV genus β (β HPV 5 and 8 E6) can disrupt p53 signaling by diminishing the steady state levels of two p53 modifying enzymes, ATR and p300. Here, we show that β-HPV 5 and 8 E6 are also capable of reducing the steady state levels of another p53 modifying enzyme, ATM, and as a result restrict LINE-1 retrotransposition. Furthermore, we show that the reduction of both ATM and LINE-1 retrotransposition is dependent upon the ability of β-HPV 8 E6 to bind and degrade p300. We use inhibitors and dominant negative mutants to confirm that ATM is needed for efficient LINE-1 retrotransposition. Furthermore, neither sensitivity to LINE-1 expression nor LINE-1 induced DSB formation is altered in an ATM deficient background. Together, these data illustrate the broad impact some β-HPVs have on DNA damage signaling by promoting p300 degradation.

Publication types

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

MeSH terms

  • Ataxia Telangiectasia Mutated Proteins
  • Betapapillomavirus / physiology*
  • Cell Cycle Proteins / antagonists & inhibitors*
  • DNA-Binding Proteins / antagonists & inhibitors*
  • HeLa Cells
  • Humans
  • Long Interspersed Nucleotide Elements*
  • Oncogene Proteins, Viral / metabolism*
  • Protein Serine-Threonine Kinases / antagonists & inhibitors*
  • Proteolysis
  • Recombination, Genetic*
  • Tumor Suppressor Proteins / antagonists & inhibitors*
  • p300-CBP Transcription Factors / antagonists & inhibitors

Substances

  • Cell Cycle Proteins
  • DNA-Binding Proteins
  • Oncogene Proteins, Viral
  • Tumor Suppressor Proteins
  • p300-CBP Transcription Factors
  • p300-CBP-associated factor
  • ATM protein, human
  • Ataxia Telangiectasia Mutated Proteins
  • Protein Serine-Threonine Kinases