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The Journal of Immunology, 1998, 161: 2953-2960.
Copyright © 1998 by The American Association of Immunologists

Isolation, Structural Characterization, and Chromosomal Mapping of the Mouse Vascular Adhesion Protein-1 Gene and Promoter1 ,2

Petri Bono3,{dagger}, Marko Salmi{dagger}, David J. Smith{ddagger}, Ilona Leppänen{dagger}, Nina Horelli-Kuitunen§, Aarno Palotie§ and Sirpa Jalkanen{dagger}

* MediCity Research Laboratories, University of Turku, {dagger} National Public Health Institute, and {ddagger} BioTie Therapies, BioCity, Turku, Finland; and § Laboratory Department of Helsinki University Hospital and Department of Clinical Chemistry, University of Helsinki, Helsinki, Finland

Vascular adhesion protein-1 (VAP-1) is an endothelial cell adhesion molecule which mediates lymphocyte binding to endothelial cells. The cloning of a mouse VAP-1 (mVAP-1) cDNA revealed that mVAP-1 is a novel 110/220 kDa transmembrane molecule with significant identity to copper-containing amine oxidases. In this work the nucleotide sequence and primary structure of the mVAP-1 gene was determined and the promoter region was structurally characterized. The isolated approximately 14.4-kb mVAP-1 gene consists of 4 exons and 3 introns. Primer extension analysis and 5' rapid amplification of cDNA ends revealed multiple transcription initiation sites in different tissues suggesting that the mVAP-1 transcription is differently regulated in different tissues. Analysis of the sequence immediately upstream of the detected transcription initiation sites showed no canonical TATA or CCAAT elements, but putative regulatory elements were found close to the detected transcription start sites. The cloning of the mVAP-1 gene reveals the first insight into the genomic organization of murine amine oxidases and will, by targeted disruption of the gene, allow us to understand better the importance of VAP-1 in leukocyte trafficking and monoamine oxidase activity for the function of the immune system.




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