Interferon-gamma priming effects in the activation and deactivation of ISGF3 in K562 cells

• Published in: The Journal of biological chemistry Vol. 268; no. 17; pp. 12380 - 12387
• Main Authors: PEI-QING GAO, SIMS, S. H, CHANG, D. C, DEISSEROTH, A. B
• Format: Journal Article
• Language: English
• Published: Bethesda, MD American Society for Biochemistry and Molecular Biology 15.06.1993
• Subjects: Base Sequence; Biological and medical sciences; Cell Nucleus - metabolism; DNA-Binding Proteins - metabolism; Enzyme Induction; Fundamental and applied biological sciences. Psychology; Humans; Interferon-alpha - pharmacology; Interferon-gamma - pharmacology; Interferon-Stimulated Gene Factor 3; Interferon-Stimulated Gene Factor 3, alpha Subunit; Interferon-Stimulated Gene Factor 3, gamma Subunit; Kinetics; Luciferases - biosynthesis; Luciferases - genetics; Models, Biological; Molecular and cellular biology; Molecular genetics; Molecular Sequence Data; Oligodeoxyribonucleotides; Promoter Regions, Genetic; Recombinant Fusion Proteins - biosynthesis; Recombinant Proteins; Transcription Factors - metabolism; Transcription. Transcription factor. Splicing. Rna processing; Transfection; Tumor Cells, Cultured; Human; Activation; Gel retardation technique; Transcription; Transcription factor; Gamma interferon
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1016/S0021-9258(18)31401-7

ISGF3 is a major protein factor which mediates the transcriptional activation of interferon-inducible genes. ISGF3 is composed of two subunits, ISGF3 gamma and ISGF3 alpha, which are stimulated by interferon-gamma (IFN-gamma) and interferon-alpha (IFN-alpha), respectively. In this paper, the effect of pretreatment of IFN-gamma on the response of K562 cells to IFN-alpha, termed "gamma-priming," is examined. Using techniques of gene transfection and mobility shift assay, we studied the gamma-priming effects on the kinetics of appearance and disappearance of (i) the protein product of a luciferase reporter gene driven by an IFN-inducible promoter and (ii) the binding of ISGF3 to the interferon-stimulated response element. We found that exposure of cells to IFN-gamma prior to IFN-alpha greatly increased both the levels and the rate of ISGF3 binding activity during the early phase of IFN-alpha treatment and caused the amount of ISGF3 bound to the interferon-stimulated response element to decrease more rapidly with time during the later phase. Such effects were reflected also on the kinetics of expression of the interferon-inducible luciferase gene induced by IFN-alpha. In order to understand the basis of these gamma-priming effects, we use an in vitro reconstitution method to examine the kinetics of the subcomponents of ISGF3 in response to different IFN treatments in K562 cells. It was found that gamma-priming not only increased the levels of ISGF3 gamma, but it also stimulated both the rates of rise and fall of the activated alpha-component of ISGF3. A molecular model is proposed to explain these findings.