The interaction between hepatitis B virus X protein and AIB1 oncogene is required for the activation of NFκB signal transduction

Biochem Biophys Res Commun. 2012 Jun 22;423(1):6-12. doi: 10.1016/j.bbrc.2012.05.021. Epub 2012 May 22.

Abstract

We identified the interaction between HBV X (HBx) protein and the oncogene AIB1 (amplified in breast cancer 1). A serine/proline motif (SSPSPS) in HBx was found to be required for the interaction. Two LXD motifs [LLXX(X)L, X means any amino acids], LLRNSL and LLDQLHTLL in AIB1 were also found to be involved in the HBx-AIB1 interaction. The HBx-AIB1 interaction was important for the activation of NFκB signal transduction, the HBx mutant that did not interact with AIB1showed dramatically lower NFκB activation activity than the WT HBx. These findings contribute to the new understanding on signal transduction activation mechanisms of HBx.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Carcinogens*
  • Carcinoma, Hepatocellular / genetics
  • Carcinoma, Hepatocellular / metabolism
  • Cell Line, Tumor
  • Conserved Sequence
  • Humans
  • Molecular Sequence Data
  • Mutation
  • NF-kappa B / metabolism*
  • Nuclear Receptor Coactivator 3 / genetics
  • Nuclear Receptor Coactivator 3 / metabolism*
  • Protein Interaction Domains and Motifs
  • Serine / genetics
  • Serine / metabolism
  • Signal Transduction
  • Trans-Activators / genetics
  • Trans-Activators / metabolism*
  • Two-Hybrid System Techniques
  • Viral Regulatory and Accessory Proteins

Substances

  • Carcinogens
  • NF-kappa B
  • Trans-Activators
  • Viral Regulatory and Accessory Proteins
  • hepatitis B virus X protein
  • Serine
  • NCOA3 protein, human
  • Nuclear Receptor Coactivator 3