Transcriptional Repression of the IL-2 Gene in Th Cells by ZEB

Author:

Yasui Dag H.1,Genetta Tom2,Kadesch Tom2,Williams Thomas M.3,Swain Susan L.4,Tsui Lisa V.4,Huber Brigitte T.1

Affiliation:

1. *Program in Immunology, Department of Pathology, Tufts University School of Medicine, Boston, MA 02111;

2. †Howard Hughes Medical Institute and Department of Genetics, University of Pennsylvania School of Medicine, Philadelphia, PA 19704;

3. ‡Department of Pathology, School of Medicine, University of New Mexico, Albuquerque, NM 87131; and

4. §Trudeau Institute, Saranac Lake, NY 12983

Abstract

AbstractTh1- and Th2-type cells mediate distinct effector functions via cytokine secretion in response to immunologic challenge. Precursor Th cells transcribe IFN-γ, IL-2, and IL-4 upon activation. Repeated stimulation of Th precursor cells in the presence of IL-4 leads to terminally differentiated Th2 cells that have lost the ability to transcribe the IL-2 gene. We provide evidence that repression of IL-2 gene expression in Th2 cells and partial repression in Th1 cells are mediated by ZEB, a zinc finger, E box-binding transcription factor. This factor binds to a negative regulatory element, NRE-A, in the IL-2 promoter, thereby acting as a potent repressor of IL-2 transcription.

Publisher

The American Association of Immunologists

Subject

Immunology,Immunology and Allergy

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