Tyramine receptor (SER‐2) isoforms are involved in the regulation of pharyngeal pumping and foraging behavior in Caenorhabditis elegans

Octopamine regulates essential processes in nematodes; however, little is known about the physiological role of its precursor, tyramine. In the present study, we have characterized alternatively spliced Caenorhabditis elegans tyramine receptor isoforms (SER‐2 and SER‐2A) that differ by 23 amino acids within the mid‐region of the third intracellular loop. Membranes prepared from cells expressing either SER‐2 or SER‐2A bind [3H]lysergic acid diethylamide (LSD) in the low nanomolar range and exhibit highest affinity for tyramine. Similarly, both isoforms exhibit nearly identical Ki values for a number of antagonists. In contrast, SER‐2A exhibits a significantly lower affinity than SER‐2 for other physiologically relevant biogenic amines, including octopamine. Pertussis toxin treatment reduces affinity for both tyramine and octopamine, especially for octopamine in membranes from cells expressing SER‐2, suggesting that the conformation of the mid‐region of the third intracellular loop is dictated by G‐protein interactions and is responsible for the differential tyramine/octopamine affinities of the two isoforms. Tyramine reduces forskolin‐stimulated cAMP levels in HEK293 cells expressing either isoform with nearly identical IC50 values. Tyramine, but not octopamine, also elevates Ca2+ levels in cells expressing SER‐2 and to a lesser extent SER‐2A. Most importantly, ser‐2 null mutants (pk1357) fail to suppress head movements while reversing in response to nose‐touch, suggesting a role for SER‐2 in the regulation of foraging behavior, and fail to respond to tyramine in assays measuring serotonin‐dependent pharyngeal pumping. These are the first reported functions for SER‐2. These results suggest that C. elegans contains tyramine receptors, that individual SER‐2 isoforms may differ significantly in their sensitivity to other physiologically relevant biogenic amines, such as octopamine (OA), and that tyraminergic signaling may be important in the regulation of key processes in nematodes.

[1]  Andrew Fire,et al.  Chapter 19 DNA Transformation , 1995 .

[2]  W. Sadee,et al.  Hydrophobic amino acid in the i2 loop plays a key role in receptor-G protein coupling. , 1993, The Journal of biological chemistry.

[3]  R. Martin,et al.  Target sites of anthelmintics , 1997, Parasitology.

[4]  H. Motulsky,et al.  Alpha 2-adrenergic receptor stimulation mobilizes intracellular Ca2+ in human erythroleukemia cells. , 1989, The Journal of biological chemistry.

[5]  J. Venter,et al.  Cloning, localization, and permanent expression of a Drosophila octopamine receptor , 1990, Neuron.

[6]  R. Kohen,et al.  Cloning of the mouse 5-HT6 serotonin receptor and mutagenesis studies of the third cytoplasmic loop. , 2001, Brain research. Molecular brain research.

[7]  H. Horvitz,et al.  A dual mechanosensory and chemosensory neuron in Caenorhabditis elegans. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[8]  R. Planta,et al.  Molecular cloning and pharmacological characterization of a molluscan octopamine receptor. , 1997, Molecular pharmacology.

[9]  K. Han,et al.  A Novel Octopamine Receptor with Preferential Expression inDrosophila Mushroom Bodies , 1998, The Journal of Neuroscience.

[10]  J. Kaplan,et al.  Distinct Signaling Pathways Mediate Touch and Osmosensory Responses in a Polymodal Sensory Neuron , 1999, The Journal of Neuroscience.

[11]  P. Evans,et al.  The expression of a cloned Drosophila octopamine/tyramine receptor in Xenopus oocytes , 1997, Brain Research.

[12]  C. Gerfen,et al.  Multiple D2 dopamine receptors produced by alternative RNA splicing , 1989, Nature.

[13]  E. Kandel,et al.  Activation of a heterologously expressed octopamine receptor coupled only to adenylyl cyclase produces all the features of presynaptic facilitation in aplysia sensory neurons. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[14]  E. Borrelli,et al.  Alternative Splicing of the Dopamine D2 Receptor Directs Specificity of Coupling to G-proteins (*) , 1995, The Journal of Biological Chemistry.

[15]  E. M. Blumenthal Regulation of chloride permeability by endogenously produced tyramine in the Drosophila Malpighian tubule. , 2003, American journal of physiology. Cell physiology.

[16]  W. N. Ross,et al.  Calcium transients in cerebellar Purkinje neurons evoked by intracellular stimulation. , 1992, Journal of neurophysiology.

[17]  Robin Shattock,et al.  In Vitro and In Vivo: The Story of Nonoxynol 9 , 2005, Journal of acquired immune deficiency syndromes.

[18]  J. Kaplan,et al.  The EGL-3 Proprotein Convertase Regulates Mechanosensory Responses of Caenorhabditis elegans , 2001, The Journal of Neuroscience.

[19]  A. Baumann,et al.  Amtyr1: characterization of a gene from honeybee (Apis mellifera) brain encoding a functional tyramine receptor. , 2000, Journal of neurochemistry.

[20]  S. Juhos,et al.  Characterization of the tyraminergic system in the central nervous system of the locust,Locusta migratoria migratoides , 1993, Neurochemical Research.

[21]  C. Strader,et al.  Identification of two serine residues involved in agonist activation of the beta-adrenergic receptor. , 1989, The Journal of biological chemistry.

[22]  P. Pauwels,et al.  Activation of constitutive 5-hydroxytryptamine(1B) receptor by a series of mutations in the BBXXB motif: positioning of the third intracellular loop distal junction and its G(o)alpha protein interactions. , 1999, The Biochemical journal.

[23]  R. Downer Trehalose production in isolated fat body of the American cockroach, Periplaneta americana. , 1979, Comparative biochemistry and physiology. C: Comparative pharmacology.

[24]  M. Caron,et al.  A highly conserved tyrosine residue in G protein-coupled receptors is required for agonist-mediated beta 2-adrenergic receptor sequestration. , 1994, The Journal of biological chemistry.

[25]  H. Horvitz,et al.  Serotonin and octopamine in the nematode Caenorhabditis elegans. , 1982, Science.

[26]  B. Roth,et al.  A single point mutation (Phe340-->Leu340) of a conserved phenylalanine abolishes 4-[125I]iodo-(2,5-dimethoxy)phenylisopropylamine and [3H]mesulergine but not [3H]ketanserin binding to 5-hydroxytryptamine2 receptors. , 1993, Molecular pharmacology.

[27]  G. Corsini,et al.  Functional Role of the Third Cytoplasmic Loop in Muscarinic Receptor Dimerization* , 1996, The Journal of Biological Chemistry.

[28]  INTERNATIONAL SOCIETY FOR NEUROCHEMISTRY , 1976 .

[29]  Amos Bairoch,et al.  ScanProsite: a reference implementation of a PROSITE scanning tool. , 2002, Applied bioinformatics.

[30]  R. Komuniecki,et al.  Characterization of a tyramine receptor from Caenorhabditis elegans , 2002, Journal of Neurochemistry.

[31]  S. Senogles The D2 dopamine receptor isoforms signal through distinct Gi alpha proteins to inhibit adenylyl cyclase. A study with site-directed mutant Gi alpha proteins. , 1994, The Journal of biological chemistry.

[32]  L. Avery,et al.  Interacting genes required for pharyngeal excitation by motor neuron MC in Caenorhabditis elegans. , 1995, Genetics.

[33]  C. A. Thomas,et al.  Molecular cloning. , 1977, Advances in pathobiology.

[34]  M. Martres,et al.  Alternative splicing directs the expression of two D2 dopamine receptor isoforms , 1989, Nature.

[35]  W. Yi,et al.  Similarity of DNA binding and transcriptional regulation by Caenorhabditis elegans MAB-3 and Drosophila melanogaster DSX suggests conservation of sex determining mechanisms. , 1999, Development.

[36]  S. Juhos,et al.  Characterization of tyramine and octopamine receptors in the insect (Locusta migratoria migratorioides) brain , 1994, Brain Research.

[37]  Robert J. Hobson,et al.  Functional characterization of alternatively spliced 5‐HT2 receptor isoforms from the pharynx and muscle of the parasitic nematode, Ascaris suum , 2002, Journal of neurochemistry.

[38]  H Weinstein,et al.  Mapping the Binding Site Pocket of the Serotonin 5-Hydroxytryptamine2A Receptor , 1996, The Journal of Biological Chemistry.

[39]  L. Avery,et al.  LIM homeobox gene-dependent expression of biogenic amine receptors in restricted regions of the C. elegans nervous system. , 2003, Developmental biology.

[40]  David R Soll,et al.  Tyramine and octopamine have opposite effects on the locomotion of Drosophila larvae. , 2004, Journal of neurobiology.

[41]  R. Porter,et al.  DNA transformation. , 1988, Methods in enzymology.

[42]  H. Horvitz,et al.  Transcriptional regulator of programmed cell death encoded by Caenorhabditis elegans gene ces-2 , 1996, Nature.

[43]  D. Grandy,et al.  Cloning and expression of a rat D2 dopamine receptor cDNA , 1988, Nature.

[44]  Alessandro Usiello,et al.  Distinct functions of the two isoforms of dopamine D2 receptors , 2000, Nature.

[45]  E. Borrelli,et al.  Cloning and characterization of a Drosophila tyramine receptor. , 1990, The EMBO journal.

[46]  Bruce Bowerman,et al.  skn-1, a maternally expressed gene required to specify the fate of ventral blastomeres in the early C. elegans embryo , 1992, Cell.

[47]  B. Roth,et al.  Identification of conserved aromatic residues essential for agonist binding and second messenger production at 5-hydroxytryptamine2A receptors. , 1997, Molecular pharmacology.

[48]  P. Evans,et al.  Agonist‐specific coupling of a cloned Drosophila octopamine/tyramine receptor to multiple second messenger systems. , 1994, The EMBO journal.

[49]  R. Hollingworth,et al.  In vitro and in vivo effects of formamidines in locust (Locusta migratoria migratorioides) , 1999, Acta biologica Hungarica.

[50]  A. De Loof,et al.  Characterization of a Cloned Locust Tyramine Receptor cDNA by Functional Expression in Permanently Transformed Drosophila S2 Cells , 1995, Journal of neurochemistry.

[51]  Robert J. Lefkowitz,et al.  Switching of the coupling of the β2-adrenergic receptor to different G proteins by protein kinase A , 1997, Nature.

[52]  A. Komatsu,et al.  A trace amine, tyramine, functions as a neuromodulator in Drosophila melanogaster , 2002, Neuroscience Letters.

[53]  S. Liggett,et al.  Role of the amino terminus of the third intracellular loop in agonist-promoted downregulation of the alpha2A-adrenergic receptor. , 1997, Biochemistry.

[54]  Susumu Tonegawa,et al.  Dopamine D2 Long Receptor-Deficient Mice Display Alterations in Striatum-Dependent Functions , 2000, The Journal of Neuroscience.

[55]  J. Nathanson Characterization of octopamine-sensitive adenylate cyclase: elucidation of a class of potent and selective octopamine-2 receptor agonists with toxic effects in insects. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[56]  J. Priess,et al.  Formation of a monomeric DNA binding domain by Skn-1 bZIP and homeodomain elements. , 1994, Science.

[57]  D. Yamamoto,et al.  A tyramine receptor gene mutation causes a defective olfactory behavior in Drosophila melanogaster. , 2000, Gene.

[58]  T. Branchek,et al.  Dual coupling of cloned human 5-hydroxytryptamine1D alpha and 5-hydroxytryptamine1D beta receptors stably expressed in murine fibroblasts: inhibition of adenylate cyclase and elevation of intracellular calcium concentrations via pertussis toxin-sensitive G protein(s). , 1993, Molecular pharmacology.