Cloning of the 5′-flanking region of the murine bone morphogenetic protein-7 gene

被引:7
|
作者
Simon, M
Feliers, D
Arar, M
Bhandari, B
Abboud, HE
机构
[1] Univ Texas, Hlth Sci Ctr, Dept Med, Div Nephrol, San Antonio, TX 78229 USA
[2] Univ Texas, Hlth Sci Ctr, Dept Med, Div Pediat Nephrol, San Antonio, TX 78229 USA
[3] S Texas Vet Hlth Care Syst, Audie Murphy Div, San Antonio, TX USA
关键词
BMP-7; bone morphogenetic protein; kidney development; transcriptional regulation; promoter activity;
D O I
10.1023/A:1015546615027
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
BMP-7, a member of the bone morphogenetic protein subfamily of the TGFbeta-superfamily is highly expressed in the murine kidney. BMP-7 is involved in fetal nephron development and mesenchymal to epithelial cell differentiation. Constitutive BMP-7 expression is found in tubular and glomerular epithelial cells of the adult kidney. BMP-7 may play a role in physiology and pathophysiology of the adult kidney since BMP-7 gene expression in acute renal ischemia is diminished and injection of recombinant BMP-7 into rats with ischemic acute renal failure preserves renal function. In order to investigate the transcriptional regulation of BMP-7, this study was undertaken to clone and characterize the promoter of the murine BMP-7 gene. A 1394 bp sequence of the 5'-flanking region of the BMP-7 gene was isolated and subcloned. No TATA and CAAT box consensus motifs could be identified as shown for promoters of other BMPs. Using in vitro transfection assays, the 5'-flanking region revealed moderate to strong basal promoter activity. PMA increased basal BMP-7 promoter activity. Thus BMP-7 gene transcription might involve at least in part a PKC-dependent pathway. The cloning of a 5'-flanking region of the BMP-7 gene should provide a useful tool for future studies on the transcriptional regulation of BMP-7 gene expression.
引用
收藏
页码:31 / 37
页数:7
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