Adenovirus E4orf4 protein binds to protein phosphatase 2A, and the complex down regulates E1A-enhanced junB transcription

J Virol. 1993 Dec;67(12):7556-60. doi: 10.1128/JVI.67.12.7556-7560.1993.

Abstract

Adenovirus E4orf4 protein was previously shown to counteract transactivation of junB by cyclic AMP (cAMP) and E1A protein. It was also shown to cause hypophosphorylation of E1A and c-Fos proteins. Here we show that the E4orf4 protein associates with protein phosphatase 2A. All three subunits of the phosphatase are present in the complex, and the B subunit interacts directly with the viral protein. The complex possesses a phosphatase activity typical of protein phosphatase 2A, and the phosphatase mediates the E4orf4-induced down regulation of junB transcription. Thus, adenovirus E4orf4 protein recruits protein phosphatase 2A into a signal transduction pathway initiated by cAMP and E1A protein.

Publication types

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

MeSH terms

  • Adenovirus E1A Proteins / metabolism*
  • Adenovirus E4 Proteins / metabolism*
  • Animals
  • Base Sequence
  • Down-Regulation*
  • Macromolecular Substances
  • Mice
  • Molecular Sequence Data
  • Phosphoprotein Phosphatases / metabolism*
  • Promoter Regions, Genetic
  • Protein Phosphatase 2
  • Proto-Oncogene Proteins c-jun / biosynthesis*
  • Proto-Oncogene Proteins c-jun / genetics
  • Tumor Cells, Cultured

Substances

  • Adenovirus E1A Proteins
  • Adenovirus E4 Proteins
  • Macromolecular Substances
  • Proto-Oncogene Proteins c-jun
  • Phosphoprotein Phosphatases
  • Protein Phosphatase 2