Regulation of Sp100A subnuclear localization and transcriptional function by EBNA-LP and interferon

J Interferon Cytokine Res. 2008 Nov;28(11):667-78. doi: 10.1089/jir.2008.0023.

Abstract

Epstein-Barr virus (EBV) efficiently immortalizes human B cells and is associated with several human malignancies. The EBV transcriptional activating protein EBNA2 and the EBNA2 coactivator EBNA-leader protein (EBNA-LP) are important for B cell immortalization. Recent observations from our laboratory indicate that EBNA-LP coactivation function is mediated through interactions with the interferon-inducible gene (ISG) Sp100, resulting in displacement from its normal location in promyelocytic leukemia nuclear bodies (PML NBs) into the nucleoplasm. The EBNA-LP- and interferon-mediated mechanisms that regulate Sp100 subnuclear localization and transcriptional function remain undefined. To clarify these issues, we generated a panel of Sp100 mutant proteins to ascertain whether EBNA-LP induces Sp100 displacement from PML NBs by interfering with Sp100 dimerization or through other domains. In addition, we tested EBNA-LP function in interferon-treated cells. Our results indicate that Sp100 dimerization, PML NB localization, and EBNA-LP interaction domains overlap significantly. We also show that IFN-beta does not inhibit EBNA-LP coactivation function. The results suggest that EBNA-LP might play a role in EBV-evasion of IFN-mediated antiviral responses.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Antigens, Nuclear / genetics*
  • Antigens, Nuclear / metabolism
  • Autoantigens / genetics*
  • Autoantigens / metabolism
  • B-Lymphocytes / metabolism*
  • B-Lymphocytes / virology
  • Cell Line
  • Cell Transformation, Neoplastic
  • Cell Transformation, Viral
  • Epstein-Barr Virus Infections / genetics
  • Epstein-Barr Virus Infections / immunology
  • Gene Expression Regulation
  • Herpesvirus 4, Human / genetics*
  • Herpesvirus 4, Human / metabolism
  • Humans
  • Interferons / genetics*
  • Interferons / metabolism
  • Protein Transport
  • Recombinant Proteins
  • Sequence Deletion
  • Transcriptional Activation
  • Viral Proteins / genetics
  • Viral Proteins / metabolism*

Substances

  • Antigens, Nuclear
  • Autoantigens
  • EBNA-LP protein, Human herpesvirus 4
  • Recombinant Proteins
  • Viral Proteins
  • SP100 protein, human
  • Interferons