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UBP43 is a novel regulator of interferon signaling independent of its ISG15 isopeptidase activity.

Interferons (IFNs) regulate diverse cellular functions through activation of the Janus kinase-signal transducer and activator of transcription (JAK-STAT) pathway. Lack of Ubp43, an IFN-inducible ISG15 deconjugating enzyme, leads to IFN hypersensitivity in ubp43-/- mice, suggesting an important function of Ubp43 in downregulation of IFN responses. Here, we show that Ubp43 negatively regulates IFN signaling independent of its isopeptidase activity towards ISG15. Ubp43 functions specifically for type I IFN signaling by downregulating the JAK-STAT pathway at the level of the IFN receptor. Using molecular, biochemical, and genetic approaches, we demonstrate that Ubp43 specifically binds to the IFNAR2 receptor subunit and inhibits the activity of receptor-associated JAK1 by blocking the interaction between JAK and the IFN receptor. These data implicate Ubp43 as a novel in vivo inhibitor of signal transduction pathways that are specifically triggered by type I IFN.

Pubmed ID: 16710296


  • Malakhova OA
  • Kim KI
  • Luo JK
  • Zou W
  • Kumar KG
  • Fuchs SY
  • Shuai K
  • Zhang DE


The EMBO journal

Publication Data

June 7, 2006

Associated Grants

  • Agency: NCI NIH HHS, Id: CA079849
  • Agency: NCI NIH HHS, Id: CA092900

Mesh Terms

  • Animals
  • Cell Line
  • Cytokines
  • Down-Regulation
  • Endopeptidases
  • Humans
  • Interferon Type I
  • Janus Kinase 1
  • Membrane Proteins
  • Mice
  • Mice, Knockout
  • Protein-Tyrosine Kinases
  • Receptor, Interferon alpha-beta
  • Receptors, Interferon
  • STAT Transcription Factors
  • Signal Transduction
  • Ubiquitin Thiolesterase
  • Ubiquitins