Human I-mfa domain proteins specifically interact with KSHV LANA and affect its regulation of Wnt signaling-dependent transcription

Biochem Biophys Res Commun. 2010 Jun 4;396(3):608-13. doi: 10.1016/j.bbrc.2010.04.111. Epub 2010 Apr 24.

Abstract

Kaposi's sarcoma-associated herpes virus (KSHV)-encoded latency-associated nuclear antigen (LANA) protein has been reported to interact with glycogen synthase kinase 3beta (GSK-3beta) and to negatively regulate its activity, leading to stimulation of GSK-3beta-dependent beta-catenin degradation. We show here that the I-mfa domain proteins, HIC (human I-mfa domain-containing protein) and I-mfa (inhibitor of MyoD family a), interacted in vivo with LANA through their C-terminal I-mfa domains. This interaction affected the intracellular localization of HIC, inhibited the LANA-dependent transactivation of a beta-catenin-regulated reporter construct, and decreased the level of the LANA.GSK-3beta complex. These data reveal for the first time that I-mfa domain proteins interact with LANA and negatively regulate LANA-mediated activation of Wnt signaling-dependent transcription by inhibiting the formation of the LANA.GSK-3beta complex.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Viral / metabolism*
  • COS Cells
  • Cell Line
  • Chlorocebus aethiops
  • Gene Expression Regulation, Viral*
  • Glycogen Synthase Kinase 3 / antagonists & inhibitors
  • Glycogen Synthase Kinase 3 / metabolism
  • Herpesvirus 8, Human / genetics*
  • Herpesvirus 8, Human / metabolism
  • Humans
  • Myogenic Regulatory Factors / metabolism*
  • Nuclear Proteins / antagonists & inhibitors
  • Nuclear Proteins / metabolism*
  • Signal Transduction
  • Transcription, Genetic*
  • Wnt Proteins / metabolism*

Substances

  • Antigens, Viral
  • MDFIC protein, human
  • Myogenic Regulatory Factors
  • Nuclear Proteins
  • Wnt Proteins
  • latency-associated nuclear antigen
  • MDFI protein, human
  • Glycogen Synthase Kinase 3