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 language | English |
|---|---|
| Pages (from-to) | 11305-11309 |
| Number of pages | 5 |
| Journal | Proceedings of the National Academy of Sciences of the United States of America |
| Volume | 88 |
| Issue number | 24 |
| State | Published - 1991 |
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