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5' regulatory region of a novel cytokine gene mediates selective activation by interferon gamma

A newly described member of the platelet factor 4 family of cytokine genes, mig, is selectively induced by interferon gamma (IFN-gamma), and not IFN-alpha, in the mouse macrophage-like cell line RAW 264.7. Treatment of RAW 264.7 cells with IFN-gamma activated mig gene transcription as determined by...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1991
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2118797/
https://www.ncbi.nlm.nih.gov/pubmed/1899103
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description A newly described member of the platelet factor 4 family of cytokine genes, mig, is selectively induced by interferon gamma (IFN-gamma), and not IFN-alpha, in the mouse macrophage-like cell line RAW 264.7. Treatment of RAW 264.7 cells with IFN-gamma activated mig gene transcription as determined by nuclear run-on assays. mig genomic clones were isolated, and constructs containing genomic fragments that included the mig promoter region and the CAT reporter gene were prepared. In RAW 264.7 cells transfected with these constructs, CAT activity was found to be selectively induced by IFN-gamma. A 278-bp genomic fragment containing 235 nucleotides 5' of the transcription start site was sufficient for IFN-gamma-selective induction of CAT activity. Analysis of 5' deletion mutants localized a region essential for activation by IFN-gamma to within 64 nucleotides extending from - 235 to -172. A genomic fragment containing this sequence was capable of conferring IFN-gamma inducibility to constructs with a heterologous promoter.
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spelling pubmed-21187972008-04-17 5' regulatory region of a novel cytokine gene mediates selective activation by interferon gamma J Exp Med Articles A newly described member of the platelet factor 4 family of cytokine genes, mig, is selectively induced by interferon gamma (IFN-gamma), and not IFN-alpha, in the mouse macrophage-like cell line RAW 264.7. Treatment of RAW 264.7 cells with IFN-gamma activated mig gene transcription as determined by nuclear run-on assays. mig genomic clones were isolated, and constructs containing genomic fragments that included the mig promoter region and the CAT reporter gene were prepared. In RAW 264.7 cells transfected with these constructs, CAT activity was found to be selectively induced by IFN-gamma. A 278-bp genomic fragment containing 235 nucleotides 5' of the transcription start site was sufficient for IFN-gamma-selective induction of CAT activity. Analysis of 5' deletion mutants localized a region essential for activation by IFN-gamma to within 64 nucleotides extending from - 235 to -172. A genomic fragment containing this sequence was capable of conferring IFN-gamma inducibility to constructs with a heterologous promoter. The Rockefeller University Press 1991-02-01 /pmc/articles/PMC2118797/ /pubmed/1899103 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Articles
5' regulatory region of a novel cytokine gene mediates selective activation by interferon gamma
title 5' regulatory region of a novel cytokine gene mediates selective activation by interferon gamma
title_full 5' regulatory region of a novel cytokine gene mediates selective activation by interferon gamma
title_fullStr 5' regulatory region of a novel cytokine gene mediates selective activation by interferon gamma
title_full_unstemmed 5' regulatory region of a novel cytokine gene mediates selective activation by interferon gamma
title_short 5' regulatory region of a novel cytokine gene mediates selective activation by interferon gamma
title_sort 5' regulatory region of a novel cytokine gene mediates selective activation by interferon gamma
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2118797/
https://www.ncbi.nlm.nih.gov/pubmed/1899103