Cloning and Characterization of the Human Interleukin-3 (IL-3)/IL-5/ Granulocyte-Macrophage Colony-Stimulating Factor Receptor bc Gene: Regulation by Ets Family Members
نویسندگان
چکیده
High-affinity receptors for interleukin-3 (IL-3), IL-5, and granulocyte-macrophage colony-stimulating factor (GM-CSF) are composed of two distinct subunits, a ligand-specific a chain and a common b chain (bc). Whereas the mouse has two homologous b subunits (bc and bIL-3), in humans, only a single b chain is identified. We describe here the isolation and characterization of the gene encoding the human IL-3/IL5/GM-CSF receptor b subunit. The gene spans about 25 kb and is divided into 14 exons, a structure very similar to that of the murine bc/bIL-3 genes. Surprisingly, we also found the remnants of a second bc chain gene directly downstream of bc. We identified a functional promoter that is active in the myeloid cell lines U937 and HL-60, but not in HeLa cells. The proximal promoter region, located from 2103 to 133 bp, contains two GGAA consensus binding sites for members of the Ets family. Single mutation of those sites reduces promoter activity by 70% to 90%. The 58 element specifically binds PU.1, whereas the 38 element binds a yet-unidentified protein. These findings, together with the observation that cotransfection of PU.1 and other Ets family members enhances bc promoter activity in fibroblasts, reinforce the notion that GGAA elements play an important role in myeloidspecific gene regulation. r 1998 by The American Society of Hematology.
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Cloning and characterization of the human interleukin-3 (IL-3)/IL-5/ granulocyte-macrophage colony-stimulating factor receptor betac gene: regulation by Ets family members.
High-affinity receptors for interleukin-3 (IL-3), IL-5, and granulocyte-macrophage colony-stimulating factor (GM-CSF) are composed of two distinct subunits, a ligand-specific chain and a common beta chain (betac). Whereas the mouse has two homologous beta subunits (betac and betaIL-3), in humans, only a single beta chain is identified. We describe here the isolation and characterization of the ...
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