Neuron
Volume 4, Issue 3, March 1990, Pages 343-354
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Article
Cloning, localization, and permanent expression of a Drosophila octopamine receptor

https://doi.org/10.1016/0896-6273(90)90047-JGet rights and content

Abstract

A cDNA for a member of the G protein-coupled receptor family was isolated from Drosophila using a probe derived from a human β2-adrenergic receptor cDNA. This Drosophila receptor gene is localized at 99A10-B1 on the right arm of chromosome 3 and is preferentially expressed in Drosophila heads. The insect octopamine receptor has been permanently expressed in mammalian cells, where it mediates the attenuation of adenylate cyclase activity and exhibits a pharmacological profile consistent with an octopamine type 1 receptor. Sequence and pharmacological comparisons indicate that the octopamine receptor is unique but closely related to mammalian adrenergic receptors, perhaps as an evolutionary precursor.

References (60)

  • P.J. Munson et al.

    LIGAND: a versatile computerized approach for the characterization of ligand binding systems

    Anal. Biochem.

    (1980)
  • J.A. Nathanson et al.

    Isolation and N-terminal amino acid sequence of an octopamine ligand binding protein

    FEBS Lett.

    (1989)
  • T. Onai et al.

    Cloning, sequence analysis and chromosome localization of a Drosophila muscarinic acetylcholine receptor

    FEBS Lett.

    (1989)
  • J.C. Venter et al.

    Evolution of neurotransmitter receptor systems

    Prog. Neurobiol.

    (1988)
  • J.C. Venter et al.

    Molecular biology of adrenergic and muscarinic cholinergic receptors. A perspective

    Biochem. Pharmacol.

    (1989)
  • R.J. Walker et al.

    The first family (adrenaline, noradrenaline, dopamine, octopamine, tyramine, phenylethanolamine and phenylethylamine)

    Comp. Biochem.

    (1978)
  • J. Axelrod et al.

    Octopamine

    nature

    (1977)
  • B. battelle et al.

    Targets of octopamine action in the lobster: cyclic nucleotide changes and physiological effects in hemolymph, heart and exoskeletal muscle

    J. Pharmacol. Exp. Ther.

    (1978)
  • B. Battelle et al.

    Neurotransmitter synthesis in Limulus ventral nerve photoreceptors

    Experientia

    (1979)
  • G. Blobel et al.

    Transfer of proteins across membranes. II. Reconstitution of functional rough microsomes from heterologous components

    J. Cell Biol.

    (1975)
  • J.R. Bunzow et al.

    Cloning and expression of a rat D2 dopamine receptor cDNA

    Nature

    (1988)
  • J.M. Chirgwin et al.

    Isolation of biologically active ribonucleic acid from sources enriched in ribonuclease

    Biochemistry

    (1979)
  • S. Cotecchia et al.

    Molecular cloning and exoression of the cDNA for the hamster alpha1-adrenergic receptor

  • W.P.C. Dao et al.

    Effect of cyproheptadine on the octopamine-induced responses in the mammalian central nervous system

    Experientia

    (1980)
  • M.O. Dayhoff et al.
  • J. Devereux et al.

    A comprehensive set of sequence analysis programs of the VAX

    Nucl. Acids Res.

    (1984)
  • R. Dixon et al.

    Cloning of the gene and cDNA for mammalian β-adrenergic receptor and homology with rhodopsin

    Nature

    (1986)
  • W.R. Engels et al.

    In situ hybridization to Drosophila salivary chromosomes with biotinylated DNA probes and alkaline phosphatase

    Focus

    (1985)
  • P.D. Evans

    Multiple receptor types for octopamine in the locust

    J. Physiol.

    (1981)
  • P.D. Evans

    Properties of modulatory octopamine receptors in the locust

    CIBA Found. Symp.

    (1982)
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    Present address: Department of Pediatrics, The Kyoto Prefectural University of Medicine, Kawaramachi, Hirokoji, Kamikyoku, Kyoto, Japan 602.

    §

    Present address: Section on Molecular Neurobiology, LPPS, NIAAA, ADAMHA, Rockville, Maryland 20852.

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