The promyelocytic leukemia protein functions as a negative regulator of IFN-γ signaling

Youn H. Choi, Rosa Bernardi, Pier Paolo Pandolfi, Etty N. Benveniste

Research output: Contribution to journalArticle

Abstract

IFN-γ is an immunomodulatory cytokine and uses the STAT-1α transcription factor to mediate gene expression. The promyelocytic leukemia (PML) protein regulates transcription as an activator or repressor, depending on the gene under investigation. Herein, we examined the influence of PML on IFN-γ signaling, using PML wild-type (Pml+/+) and deficient (Pml-/-) mouse embryonic fibroblasts (MEF). Pml-/- MEF exhibit enhanced IFN-γ-induced STAT-1α transcriptional activity compared with Pml+/+ cells. Moreover, reconstitution of PML in Pml-/- MEF reduced STAT-1α transcriptional activity to levels comparable to Pml+/+ MEF. Numerous endogenous IFN-γ-regulated genes were up-regulated in Pml-/- MEF compared with Pml+/+ MEF. IFN-γ-mediated STAT-1α DNA-binding activity was enhanced in Pml-/- cells compared with Pml+/+ cells. Lastly, IFN-γ enhanced the formation of a PML-STAT-1α complex in the nucleus. These data suggest a novel function for PML in the IFN-γ signaling pathway by inhibiting STAT-1α DNA binding and transcriptional activity.

Original languageEnglish
Pages (from-to)18715-18720
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume103
Issue number49
DOIs
Publication statusPublished - Dec 5 2006

Keywords

  • Signal transduction
  • STAT

ASJC Scopus subject areas

  • General
  • Genetics

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