Identification and characterization of a novel amphioxus dopamine D-like receptor

• Published in: Journal of neurochemistry Vol. 111; no. 1; pp. 26 - 36
• Main Authors: Burman, Chloe, Reale, Vincenzina, Srivastava, Deepak P, Evans, Peter D
• Format: Journal Article
• Language: English
• Published: England 01-10-2009
• Subjects: Amino Acid Sequence; Animals; Calcium - metabolism; Cell Line, Transformed; Chordata, Nonvertebrate - genetics; Chordata, Nonvertebrate - metabolism; Cloning, Molecular - methods; Cricetinae; Cricetulus; Cyclic AMP - metabolism; Dopamine - pharmacology; Dopamine Agents - pharmacology; Dose-Response Relationship, Drug; Enzyme Inhibitors - pharmacology; Extracellular Signal-Regulated MAP Kinases - metabolism; Gene Expression Regulation; Membrane Potentials - drug effects; Membrane Potentials - genetics; Molecular Sequence Data; Oocytes; Receptors, Dopamine D5 - genetics; Receptors, Dopamine D5 - metabolism; Transfection; Xenopus
• ISSN: 1471-4159
• DOI: 10.1111/j.1471-4159.2009.06295.x

Dopamine receptors function to control many aspects of motor control and other forms of behaviour in both vertebrates and invertebrates. They can be divided into two main groups (D(1) and D(2)) based on sequence similarity, ligand affinity and effector coupling. However, little is known about the pharmacology and functionality of dopamine receptors in the deuterostomian invertebrates, such as the cephalochordate amphioxus (Branchiostoma floridae) which has recently been placed as the most basal of all the chordates. A bioinformatic study shows that amphioxus has at least three dopamine D(1)-like receptor sequences. One of these receptors, AmphiD(1)/beta, was found to have high levels of sequence similarity to both vertebrate D(1) receptors and to beta-adrenergic receptors. Here, we report on the cloning of AmphiD(1)/beta from an adult amphioxus cDNA library, and its pharmacological characterization subsequent to its expression in both mammalian cell lines and Xenopus oocytes. It was found that AmphiD(1)/beta has a similar pharmacology to vertebrate D(1) receptors, including responding to benzodiazepine ligands. The pharmacology of the receptor exhibits 'agonist-specific coupling' depending upon the second messenger pathway to which it is linked. Moreover, no pharmacological characteristics were observed to suggest that AmphiD(1)/beta may be an amphioxus orthologue of vertebrate beta-adrenergic receptors.