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

作者信息

Ding Wei, Bellusci Saverio, Shi Wei, Warburton David

机构信息

Developmental Biology Program, Saban Research Institute, Childrens Hospital Los Angeles, and Department of Pediatric Surgery, University of Southern California Keck School of Medicine and School of Dentistry, 90027, USA.

出版信息

Am J Physiol Lung Cell Mol Physiol. 2004 Jul;287(1):L52-9. doi: 10.1152/ajplung.00430.2003. Epub 2004 Feb 20.

Abstract

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.

摘要

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