Genomic structure and promoter characterization of the human Sprouty4 gene, a novel regulator of lung morphogenesis

被引:18
作者
Ding, W
Bellusci, S
Shi, W
Warburton, D
机构
[1] Univ So Calif, Dev Biol Program, Saban Res Inst,Childrens Hosp Los Angeles, Dept Pediat Surg,Keck Sch Med, Los Angeles, CA 90027 USA
[2] Univ So Calif, Keck Sch Dent, Los Angeles, CA 90027 USA
关键词
lung development; transcription initiation site; homology analysis; reporter gene assay; transcription factor binding site;
D O I
10.1152/ajplung.00430.2003
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The expression of Sprouty4 (Spry4), an intracellular FGF receptor antagonist, shows a temporally and spatially restricted pattern in embryonic lung and is induced by ERK signaling. To clarify the molecular mechanisms regulating Spry4 transcription, the genomic structure of the human Sprouty4 (hSpry4) gene was first determined by using the GenomeWalker kit. The hSpry4 gene spans >14 kb and is organized in three exons and two introns. Multiple transcription start sites were subsequently mapped by 5'-rapid amplification of cDNA ends. Analysis of up to 4 kb of sequence in the 5'-flanking region of the gene showed the presence of multiple potential transcription factor binding sites but no TATA or CAAT boxes. Transient transfection using luciferase reporter gene constructs with progressive deletions of the hSpry4 5'-flanking region revealed that the core promoter activity is located within the proximal 0.4-kb region, whereas the minimal ERK-inducible promoter activity is between -69 and -31. Homology analysis further showed that the core promoter region of the hSpry4 gene exhibits significant similarity to the 5'-flanking region of the mouse gene.
引用
收藏
页码:L52 / L59
页数:8
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