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Nucleic Acids Research, 1993, Vol. 21, No. 24 5694-5704
© 1993


MOLECULAR BIOLOGY

Multiple closely-linked NFAT/octamer and HMG I(Y) binding sites are part of the interleukin-4 promoter

Sergei Chuvpilo+, Christof Schomberg, Rainer Gerwig1, Annette Heinfling, Raymond Reeves2, Friedrich Grummt1 and Edgar serf ling*

Institute of Pathology,University of Wuürzburg J.-Schneider-Str. 7, D-97080 Wurzburg, Germany 1Institute of Biochemistry, Biozentrum, Am Hubland, University of Wurzburg J.-Schneider-Str. 7, D-97080 Wurzburg, Germany 2National Institute of Child Health and Human Development Bethesda, MD 20892, USA

*To whom correspondence should be addressed

Received August 16, 1993. Revised October 28, 1993. Accepted October 28, 1993.

We show here that the immediate upstream region (from position - 1 2 to -270) of the murine Interleukin 4 (II-4) gene harbors a strong cell-type specific transcriptional enhancer. In T lymphoma cells, the activity of the II-4 promoter/enhancer is stimulated by phorbol esters, Ca++ ionophores and agonists of protein kinase A and inhibited by low doses of the immunosuppressant cyclosporin A. The II-4 promoter/enhancer is transcriptionally inactive in B lymphoma cells and HeLa cells. DNase I footprint protection experiments revealed six sites of the II-4 promoter/enhancer to be bound by nuclear proteins from lymphoid and myeloid cells. Among them are four purine boxes which have been described to be important sequence motifs of the II-2 promoter. They contain the motif GGAAA and are recognized by the inducible and cyclosporin A-sensitive transcription factor NFAT-1. Three of the II-4 NFAT-1 sites are closely linked to weak binding sites of Octamer factors. Several purine boxes and an AT-rich protein-binding site of the II-4 promoter are also recognized by the high mobility group protein HMG I(Y). Whereas the binding of NFAT-1 and Octamer factors enhance the activity of the II-4 promoter, the binding of HMG I(Y) suppresses its activity and, therefore, appears to be involved in the suppression of II-4 transcription in resting T lymphocytes.


+On leave from the Shemyakin Institute of Bioorganic Chemistry, Vavilov Street, Moscow, Russia


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