Abstract
We find that a short enhancer element containing the NF-κB binding site from the interleukin-2 receptor α-chain gene (IL-2Rα) is preferentially activated in T cells. The IL-2Rα enhancer binds NF-κB poorly and is only weakly activated by the NF-κB site alone. Serum response factor (SRF) binds to a site adjacent to the NF-κB site in the IL-2R enhancer, and both sites together have strong transcriptional activity specifically in T cells. Surprisingly, the levels of SRF constitutively expressed in T cells are consistently higher than in other cell types. Overexpression of SRF in B cells causes the IL-2R enhancer to function as well as it does in T cells, suggesting that the high level of SRF binding in T cells is functionally important.
Original language | English (US) |
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Pages (from-to) | 2536-2545 |
Number of pages | 10 |
Journal | Molecular and cellular biology |
Volume | 13 |
Issue number | 4 |
DOIs | |
State | Published - 1993 |
Externally published | Yes |
ASJC Scopus subject areas
- Molecular Biology
- Cell Biology