Open AccessProteome analysis reveals ubiquitin‐conjugating enzymes to be a new family of interferon‐α‐regulated genes
Author(s) -
Nyman Tuula A.,
Matikainen Sampsa,
Sareneva Timo,
Julkunen Ilkka,
Kalkkinen Nisse
Publication year - 2000
Publication title -
european journal of biochemistry
Language(s) - English
Resource type - Journals
eISSN - 1432-1033
pISSN - 0014-2956
DOI - 10.1046/j.1432-1327.2000.01433.x
Subject(s) - isg15 , cycloheximide , biology , microbiology and biotechnology , ubiquitin , interferon , ubiquitin conjugating enzyme , downregulation and upregulation , gene , protein biosynthesis , virology , biochemistry , ubiquitin ligase
Interferon (IFN)‐α is a cytokine with antiviral, antiproliferative, and immunomodulatory properties, the functions of which are mediated via IFN‐induced protein products. We used metabolic labeling and two‐dimensional gel electrophoresis followed by MS and database searches to identify potentially new IFN‐α‐induced proteins in human T cells. By this analysis, we showed that IFN‐α induces the expression of ubiquitin cross‐reactive protein (ISG15) and two ubiquitin‐conjugating enzymes, UbcH5 and UbcH8. Northern‐blot analysis showed that IFN‐α rapidly enhances mRNA expression of UbcH5, UbcH6 and UbcH8 in T cells. In addition, these genes were induced in macrophages in response to IFN‐α or IFN‐γ stimulation or influenza A or Sendai virus infections. Similarly, IFNs enhanced UbcH8 mRNA expression in A549 lung epithelial cells, HepG2 hepatoma cells, and NK‐92 cells. Cycloheximide, a protein synthesis inhibitor, did not block IFN‐induced upregulation of UbcH8 mRNA expression, suggesting that UbcH8 is the primary target gene for IFN‐α and IFN‐γ. Ubiquitin conjugation is a rate‐limiting step in antigen presentation and therefore the upregulation of UbcHs by IFNs may contribute to the enhanced antigen presentation by macrophages. Our results show that proteome analysis of cells is a suitable method for identifying previously unrecognized cytokine‐inducible genes.