Analysis of 5′-flanking region of human Smad4 (DPC4) gene

被引:16
|
作者
Minami, R [1 ]
Kitazawa, R [1 ]
Maeda, S [1 ]
Kitazawa, S [1 ]
机构
[1] Kobe Univ, Sch Med, Dept Pathol 2, Chuo Ku, Kobe, Hyogo 6500017, Japan
关键词
Smad45 promoter region; 5 '-flanking region;
D O I
10.1016/S0167-4781(98)00217-6
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
Among the transducers of the transforming growth factor (TGF)-beta/bone morphogenetic protein (BMP) receptor signaling proteins, Smad4 and Smad1 act together in BMP 2/4 signaling pathways, and Smad4 and Smad2 act in TGF-beta/activin signaling. To investigate how the Smad it gene is regulated at the transcriptional level, we cloned and characterized its 5'-flanking region. The major transcription start site mapped by primer extension analysis was 132 bp upstream of the translation start site. The promoter region lacked canonical TATA and GC boxes; it did, however, contain a TATA-like structure (TAAAAT) 32 bp upstream of the transcription start site. A consensus sequence for homeoprotein HoxA-5 (TTTAAAAATTA) was identified at 171 bp upstream of the transcription start site. Within 600 bp upstream of the transcription start site, two Pit-1 and four F2F binding sites were found. One putative AP-I site was located at -1129. These findings suggest that these homeoproteins could conduct their signals specifically by controlling both inter- and intracellular signal transduction pathways. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:182 / 185
页数:4
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