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The Journal of Immunology, 2003, 170: 334-340.
Copyright © 2003 by The American Association of Immunologists

Regulation of Cell Type-Specific Mouse Fc{epsilon}RI {beta}-Chain Gene Expression by GATA-1 Via Four GATA Motifs in the Promoter1

Keiko Maeda*, Chiharu Nishiyama2,*, Tomoko Tokura*, Yushiro Akizawa*, Makoto Nishiyama{dagger}, Hideoki Ogawa*, Ko Okumura* and Chisei Ra*,{ddagger}

* Atopy (Allergy) Research Center, Juntendo University School of Medicine, {dagger} Biotechnology Research Center, University of Tokyo, and {ddagger} Department of Molecular Cell Immunology and Allergology, Advanced Medical Research, Nihon University School of Medicine, Tokyo, Japan

The FcR {beta}-chain, a subunit of two related multisubunit receptor complexes, the Fc{epsilon}RI and Fc{gamma}RIII, amplifies the mast cell response and is necessary for the cell surface expression of Fc{epsilon}RI in mouse. The transient reporter assay indicated that -69/+4 region is required for cell type-specific transcriptional regulation of mouse {beta}-chain gene. EMSA using Abs against transcription factors or competitive oligonucleotides demonstrated that -58/-40 region (containing overlapping three GATA-1 sites, -53/-48, -46/-51, and -42/-47) and -31/-26 region (containing one GATA-1 site) are recognized by GATA-1. The promoter activity of {beta}-chain was decreased by nucleotide replacements of the GATA-1 sites in mouse mast cell line PT18. Furthermore, exogenously produced GATA-1 up-regulated the promoter activity in CV-1 cells, which are negative in the {beta}-chain production and the up-regulation was apparently suppressed by GATA-1 site mutations. These results indicate that cell type-specific transcription of mouse {beta}-chain gene is regulated by GATA-1.




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