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Characterization of the promoter of the human gene encoding the high-affinity IgG receptor: Transcriptional induction by γ-interferon is mediated through common DNA response elements

  • Memorial Sloan-Kettering Cancer Center

Research output: Contribution to journal › Article › peer-review

165 Scopus citations

Abstract

Expression of the high-affinity receptor for IgG (FcγRI) is restricted to cells of myeloid lineage and is induced by γ-interferon (IFN-γ) but not by IFN-α/β. The organization of the human FcγRI gene has been determined and the DNA elements governing its cell type-restricted transcription and IFN-γ induction are reported here. A 39-nucleotide sequence (IFN-γ response region, or GRR) is defined that is both necessary and sufficient for IFN-γ inducibility. Sequence analysis of the GRR reveals the presence of promoter elements initially defined for the major histocompatibility complex class II genes: i.e., X, H, and γ-IRE sequences. Comparison of a number of genes whose expression is induced selectively by IFN-γ indicates that the presence of these elements is a general feature of IFN-γ-responsive genes. Our studies suggest that the combination of X, H, and γ-IRE elements is a common motif in the pathway of transcriptional induction by this lymphokine.

Original languageEnglish
Pages (from-to)11305-11309
Number of pages5
JournalProceedings of the National Academy of Sciences of the United States of America
Volume88
Issue number24
StatePublished - 1991

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