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The Murine Interleukin-3 Receptor α Subunit Gene: Chromosomal Localization, Genomic Structure, and Promoter Function

The interleukin-3 receptor (IL-3R) is composed of α and β subunits, members of the class I cytokine receptor family. Here we describe isolation and characterization of the chromosomal gene for the mouse IL-3R α subunit (mlL-3Rα). Whereas the human IL-3Rα gene is tightly linked with the granulocyte-m...

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Bibliographic Details
Published in:Blood 1995-03, Vol.85 (5), p.1246-1253
Main Authors: Miyajima, Ikuko, Levitt, Lee, Hara, Takahiko, Bedell, Mary A., Copeland, Neal G., Jenkins, Nancy A., Miyajima, Atsushi
Format: Article
Language:English
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Summary:The interleukin-3 receptor (IL-3R) is composed of α and β subunits, members of the class I cytokine receptor family. Here we describe isolation and characterization of the chromosomal gene for the mouse IL-3R α subunit (mlL-3Rα). Whereas the human IL-3Rα gene is tightly linked with the granulocyte-macrophage colony-stimulating factor receptor α subunit (GM-CSFRα) gene in the pseudoautosomal region of the X and Y chromosomes, the mlL-3Rα gene (II3ra) is located in the proximal region of mouse chromosome 14, separated from the mouse GM-CSFRα gene, which is on chromosome 19. The mlL-3Rα gene spans about 10 kb and is divided into 12 exons. All the exon-intron boundaries possess the splicing junction consensus sequences (5'GT-AG3'), and the whole genomic structure is similar to those of the previously reported class I cytokine receptor genes. There are two major transcription initiation sites that are located at 215 and 188 nucleotides upstream of the initiator codon. The promoter region is GC-rich and contains potential binding sites for GATA, Ets, c-myb, Sp1, Ap-2, and G-C boxes, but not a typical TATA or CAAT sequence. A fusion gene containing 0.8 kb of the 5' noncoding sequence linked to the firefly luciferase gene directed the transcription in mouse mast cells but not in fibroblasts or T cells, suggesting that this promoter functions in a cell type-specific manner. Further sequential deletion of the 5' region suggests two potential regulatory regions for transcription of the mlL-3Rα gene.
ISSN:0006-4971
1528-0020
DOI:10.1182/blood.V85.5.1246.bloodjournal8551246