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Characterization of the murine A1 adenosine receptor promoter, potent regulation by GATA-4 and Nkx2.5.

作者信息

Rivkees S A, Chen M, Kulkarni J, Browne J, Zhao Z

机构信息

Yale University School of Medicine, Division of Pediatric Endocrinology, New Haven, Connecticut 06520, USA.

出版信息

J Biol Chem. 1999 May 14;274(20):14204-9. doi: 10.1074/jbc.274.20.14204.

Abstract

Adenosine acts via A1 adenosine receptors (A1ARs) in the heart and brain to potently influence mammalian physiology. A1ARs are expressed very early in embryonic development, and A1ARs are among the earliest expressed G protein coupled receptors in the heart and brain. To understand the biologic basis of A1AR expression, a genomic fragment containing the murine A1AR promoter was cloned. Reporter assay studies using DDT1 MF2 cells that express A1ARs revealed that 500 base pairs of the proximal A1AR promoter contained essential elements for A1AR gene expression. Transgenic mice with A1AR proximal promoter coupled with the beta-galactosidase reporter gene had heavy labeling of the brain and atria, consistent with normal patterns of A1AR expression. Within the proximal A1AR promoter, putative binding sites for cardiac transcription factors GATA and Nkx2.5 were identified. Co-expression studies revealed that GATA-4 and Nkx2.5 could individually drive A1AR promoter activity and act synergistically to activate A1AR expression. These observations suggest that embryonic A1AR expression involves activation of the A1AR promoter by GATA-4 and Nkx2.5.

摘要

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