Analysis of the 5′ promoters for human IL-3 and GM-CSF receptor α genes

被引:6
作者
Akagawa, E [1 ]
Muto, A [1 ]
Arai, K [1 ]
Watanabe, S [1 ]
机构
[1] Univ Tokyo, Inst Med Sci, Dept Mol & Dev Biol, Tokyo, Japan
关键词
haematopoietic cell; cytokine receptor; transcription; IL-3; receptor; GM-CSF receptor; TF-1; EMSA; luciferase; Sp1; PU.1;
D O I
10.1016/S0006-291X(02)02890-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The receptors for human interleukin-3 (hIL-3R) and granulocyte-macrophage colony-stimulating factor (hGM-CSFR) consist of an x subunit, specific for each cytokine, and a beta subunit, common to IL-3, GM-CSF and IL-5. We cloned genomic DNA covering 1.5 kb of the 5' flanking region of the hIL-3Rx gene and identified multiple transcription start sites by 5'-RACE and primer extension analyses. By use of transient transfection experiments, two regions (nt -363 to -331 and -106 to -92) of the hIL-3Rx promoter appeared to have significant transcription-enhancing activities. Electrophoresis mobility shift assays revealed the binding of Sp1 and unidentified proteins to these regions. Deletion of a putative PU.1 binding site did not affect the promoter activity. We then analyzed 2.5 kb of the hGM-CSFR x gene and found the proximal PU.1 binding site to be important for transcription-enhancing activity, as previously reported. These results suggest that different transcriptional activation mechanisms Lire employed for the transcriptional regulation of hIL-3 and hGM-CSF receptor x genes. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:600 / 608
页数:9
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