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PMID: 2464596 Published · ppublish English Comparative Study Journal Article Research Support, Non-U.S. Gov't

Phorbol ester-mediated down-regulation of an interferon-inducible gene.

The Journal of biological chemistry ·Vol. 264 ·No. 6 ·1989-02-25 ·Pages 3252-5

Akai H, Larner AC

Abstract

Interferons (IFNs) induce the expression of a variety of cellular RNAs and inhibit phorbol ester induction of other genes. Experiments reported here indicate that phorbol esters can also specifically inhibit the expression of an IFN-induced RNA (IFN-IND-1). Phorbol esters exert their effects by inhibiting IFN-induced transcription of the gene that encodes IFN-IND-1 (ISG-54K); inhibitors of protein synthesis reverse the effects of these compounds. The actions of phorbol esters are only seen in those types of cultured cells where cycloheximide in the presence of IFN prevents long term IFN treatment of cells from inducing a "desensitized state." In desensitized cells, IFN is not able to reinduce the transcription of the RNA. Our results indicate that a protein kinase C-dependent pathway requiring protein synthesis may be one mechanism by which IFN is able to down regulate the transcription of genes whose expression it initially induces.

MeSH Terms
Cycloheximide/pharmacology Fibroblasts/metabolism Gene Expression Regulation/drug effects Humans Interferon Type I/pharmacology Melanoma Phorbol 12,13-Dibutyrate/pharmacology RNA/biosynthesis,genetics Recombinant Proteins Tetradecanoylphorbol Acetate/pharmacology Transcription, Genetic/drug effects Tumor Cells, Cultured
Chemicals
Interferon Type I Recombinant Proteins Phorbol 12,13-Dibutyrate RNA Cycloheximide Tetradecanoylphorbol Acetate
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Akai H
Laboratory of Pathology, National Cancer Institute, Bethesda, Maryland 20892.
Larner A C
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1989-02-25
Pages
3252-5
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
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