Autor: |
Stranick, Kimberly S., Uss, Annette Schettino, Zambas, Demetris N., Egan, Robert W., Billah, M.Motasim, Umland, Shelby P. |
Zdroj: |
Biochemical and Biophysical Research Communications; November 1998, Vol. 252 Issue: 1 p56-62, 7p |
Abstrakt: |
The proximal mouse IL-5 promoter was examined using a mouse TH2 clone stimulated through the T cell receptor using anti-CD3 monoclonal antibody. DNase I protection defined four protein binding regions [IL-5RE-A, -69/-45; -B, (-90/-76); -C, (-154/-130); and -D (-176/-157)]. Stimulation-dependent binding, which was seen in the IL-5RE-B, -D regions and the 5′ end of tIL-5RE-A, did not require new protein synthesis inhibitor during cell activation. EMSA using probes targeted to the IL-5RE-B, -C, -D regions demonstrated the multimeric nature of the bound proteins. By transfection analysis using a series of truncated IL-5 promoter-luciferase constructs, IL-5RE-C and -D contributed little to constitutive or inducible activity. The CLE0 site in the IL-5RE-A region contributed to full transcriptional activity but was not sufficient to mediate full activity. Full stimulation-dependent activity required the IL-5RE-B region and/or the GATA site (-70/-60). |
Databáze: |
Supplemental Index |
Externí odkaz: |
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