Characterization of the promoter region of the human melanocortin-l receptor(MC1R) gene

被引:43
作者
Moro, O [1 ]
Ideta, R [1 ]
Ifuku, O [1 ]
机构
[1] Shiseido Res Ctr, Kohoku Ku, Yokohama, Kanagawa 2238553, Japan
关键词
D O I
10.1006/bbrc.1999.1228
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
We sequenced 3201 bp upstream from the ATG translation start codon of the human melanocortin-1 receptor (MC1R). A number of transcriptional initiation sites were detected over a region of similar to 600 base pairs upstream of the receptor coding region. These consist of GC-rich regions, each including SP-1 consensus binding motifs. Neither a TATA nor a CAAT box was found in this region. The 5'-flanking region also contains the consensus regulatory elements for AP-1, AP-2, and several E-boxes. Gel shift assays targeting the three GC boxes confirmed binding of SP-1. A promoter assay revealed that the minimal region exhibiting promoter activity was located between nucleotides -517 and -282 in human melanoma SK-Mel-2 cells. Further deletion from -517 to -447, which removed an SP-1 site, completely abolished luciferase activity. In conclusion, the MC1R promoter shares the characteristics of many other GPCR promoters. These characteristics include GC-rich sequence, lack of a TATA box, and binding of SP-1. (C) 1999 Academic Press.
引用
收藏
页码:452 / 460
页数:9
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