MOLECULAR-CLONING OF THE HUMAN AH RECEPTOR GENE PROMOTER

被引:28
|
作者
EGUCHI, H
HAYASHI, SI
WATANABE, J
GOTOH, O
KAWAJIRI, K
机构
[1] Department of Biochemistry, Saitama Cancer Center Research Institute, Saitama 362, Komuro 818, Inamachi, Kitaadachi-gun
关键词
D O I
10.1006/bbrc.1994.2227
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
A lambda phage clone containing a promoter region of the human Ah receptor gene was isolated. This clone spanned 13.8 kb and contained the Ist exon, the sequence of which completely matched the reported Ah receptor cDNA. Using RNase protection assay and primer extension analysis, the transcription initiation sites were determined to be 643 and 615 bp upstream of the translational initiation codon ATG. This promoter did not contain a TATA box, while multiple GC boxes were present close to the determined transcription initiation sites. Comparison of the 5' flank sequence of the human Ah receptor with its murine equivalent showed several well conserved regions, containing binding sites for known transcription factors, such as Spl. The promoter activity was confirmed by transient transfection of chimeric constructs of the Ah receptor gene and reporter gene luciferase into hepatoma HepG2 cells. (C) 1994 Academic Press, Inc.
引用
收藏
页码:615 / 622
页数:8
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