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Mol. Biol. Evol. 21(1):14-28. 2004
DOI: 10.1093/molbev/msg224
© 2004 by the Society for Molecular Biology and Evolution. ISSN: 0737-4038

Identification of Duplicated Fourth {alpha}2-Adrenergic Receptor Subtype by Cloning and Mapping of Five Receptor Genes in Zebrafish

Jori O. Ruuskanen*,{dagger}, Henri Xhaard{ddagger}, Anne Marjamäki*,1, Erik Salaneck§, Tiina Salminen{ddagger}, Yi-Lin Yan|, John H. Postlethwait|, Mark S. Johnson{ddagger}, Dan Larhammar§ and Mika Scheinin*

* Department of Pharmacology and Clinical Pharmacology
{dagger} Turku Graduate School of Biomedical Sciences, University of Turku, Turku, Finland
{ddagger} Department of Biochemistry and Pharmacy, Åbo Akademi University, Turku, Finland
§ Department of Neuroscience, Unit of Pharmacology, Uppsala University, Uppsala, Sweden
| Institute of Neuroscience, University of Oregon, Eugene, Oregon

E-mail: mschein{at}utu.fi.

The {alpha}2-adrenergic receptors ({alpha}2-ARs) belong to the large family of rhodopsinlike G-protein–coupled receptors that share a common structure of seven transmembrane (TM) {alpha}-helices. The aims of this study were (1) to determine the number of {alpha}2-AR genes in a teleost fish, the zebrafish (Danio rerio), (2) to study the gene duplication events that generated the {alpha}2-AR subtypes, and (3) to study changes in receptor structure that have occurred since the divergence of the mammalian and fish lineages. Here, we report the cloning and chromosomal mapping of fish orthologs for all three mammalian {alpha}2-ARs. In addition, we identified a fourth {alpha}2-AR subtype with two duplicates in zebrafish. Chromosomal mapping showed that the zebrafish {alpha}2-AR genes are located within conserved chromosomal segments, consistent with the origin of the four {alpha}2-AR subtypes by two rounds of chromosome or block duplication before the divergence of the ray fin fish and tetrapod lineages. Thus, the fourth subtype has apparently been present in the common ancestor of vertebrates but has been deleted or is yet to be identified in mammals. The overall percentage identity between the fish and mammalian orthologs is 53% to 67%, and in the TM regions 80% to 87%. These values are clearly lower than what is observed between mammalian orthologs. Still, all of the residues thought to be important for {alpha}2-adrenergic ligand binding are conserved across species and subtypes, and even the most divergent regions of the fish receptors show clear "molecular fingerprints" typical for orthologs of a given subtype.

Key Words: genome duplication • synteny • fish • {alpha}2-adrenergic receptor


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