PubMed:8943243 JSONTXT

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{"target":"https://pubannotation.org/docs/sourcedb/PubMed/sourceid/8943243","sourcedb":"PubMed","sourceid":"8943243","source_url":"http://www.ncbi.nlm.nih.gov/pubmed/8943243","text":"The proximal regulatory element of the interferon-gamma promoter mediates selective expression in T cells.\nInterferon-gamma (IFN-gamma) is produced by natural killer cells and certain subsets of T cells, but the basis for its selective expression is unknown. Within the region between -108 and -40 base pairs of the IFN-gamma promoter are two conserved and essential regulatory elements, which confer activation-specific expression in T cells. This report describes studies indicating that the most proximal of these two regulatory elements is an important determinant of its restricted expression. The proximal element is a composite site that binds members of the CREB/ATF, AP-1, and octamer families of transcription factors. Jun is essential for activation-induced transcription and binds preferably as a heterodimer with ATF-2. In contrast, CREB appears to dampen transcription from this element. The CpG dinucleotide in this element is selectively methylated in Th2 T cells and other cells that do not express IFN-gamma, and methylation markedly reduces transcription factor binding. 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