Characterization of a β-adrenergic-like octopamine receptor from the rice stem borer (Chilo suppressalis)

Journal of Experimental Biology

Volumn 215, Issue 15, 2012, Pages 2646-2652

  Wu, Shun Fan ^a   Yao, Yao ^a   Huang, Jia ^a   Ye, Gong Yin ^a  

^a ZHEJIANG UNIVERSITY   (China)

Author keywords

Antagonist; Biogenic amine; Cyclic AMP; Insecticide; Locomotion

Indexed keywords

BETA ADRENERGIC RECEPTOR; CYCLIC AMP; LIGAND; NORSYNEPHRINE RECEPTOR; RECEPTOR;

AMINO ACID SEQUENCE; ANIMAL; ANIMAL BEHAVIOR; ARTICLE; BIOASSAY; CELL STRAIN HEK293; CHEMISTRY; GENE EXPRESSION PROFILING; GENE EXPRESSION REGULATION; GENETICS; HUMAN; LOCOMOTION; METABOLISM; MOLECULAR CLONING; MOLECULAR GENETICS; MOTH; NUCLEOTIDE SEQUENCE; PARASITOLOGY; PHYLOGENY; PHYSIOLOGY; PLANT STEM; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; RICE; SEQUENCE ALIGNMENT; SEQUENCE HOMOLOGY;

AMINO ACID SEQUENCE; ANIMALS; BEHAVIOR, ANIMAL; BIOLOGICAL ASSAY; CLONING, MOLECULAR; CYCLIC AMP; GENE EXPRESSION PROFILING; GENE EXPRESSION REGULATION; HEK293 CELLS; HUMANS; LIGANDS; LOCOMOTION; MOLECULAR SEQUENCE DATA; MOTHS; ORYZA SATIVA; PHYLOGENY; PLANT STEMS; RECEPTORS, ADRENERGIC, BETA; RECEPTORS, BIOGENIC AMINE; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; SEQUENCE ALIGNMENT; SEQUENCE HOMOLOGY, AMINO ACID;

CHILO SUPPRESSALIS; HEXAPODA; INVERTEBRATA;

EID: 84863891944     PISSN: 00220949     EISSN: None     Source Type: Journal    
DOI: 10.1242/jeb.068932     Document Type: Article

References (37)

1. Bischof, L. J. and Enan, E. E. (2004). Cloning, expression and functional analysis of an octopamine receptor from Periplaneta americana. Insect Biochem. Mol. Biol. 34, 511-521.
2. Blenau, W., Balfanz, S. and Baumann, A. (2000). Amtyr1: characterization of a gene from honeybee (Apis mellifera) brain encoding a functional tyramine receptor. J. Neurochem. 74, 900-908.
3. Cazzamali, G., Klaerke, D. A. and Grimmelikhuijzen, C. J. (2005). A new family of insect tyramine receptors. Biochem. Biophys. Res. Commun. 338, 1189-1196.
4. Certel, S. J., Leung, A., Lin, C. Y., Perez, P., Chiang, A. S. and Kravitz, E. A. (2010). Octopamine neuromodulatory effects on a social behavior decision-making network in Drosophila males. PLoS ONE 5, e13248.
5. Chen, X., Ohta, H., Ozoe, F., Miyazawa, K., Huang, J. and Ozoe, Y. (2010). Functional and pharmacological characterization of a β-adrenergic-like octopamine receptor from the silkworm Bombyx mori. Insect Biochem. Mol. Biol. 40, 476-486.
6. Crocker, A. and Sehgal, A. (2008). Octopamine regulates sleep in Drosophila through protein kinase A-dependent mechanisms. J. Neurosci. 28, 9377-9385.
7. Crocker, A., Shahidullah, M., Levitan, I. B. and Sehgal, A. (2010). Identification of a neural circuit that underlies the effects of octopamine on sleep:wake behavior. Neuron 65, 670-681.
8. Enan, E. E. (2005). Molecular response of Drosophila melanogaster tyramine receptor cascade to plant essential oils. Insect Biochem. Mol. Biol. 35, 309-321.
9. Evans, P. D. (1981). Multiple receptor types for octopamine in the locust. J. Physiol. 318, 99-122.
10. Evans, P. D. and Maqueira, B. (2005). Insect octopamine receptors: a new classification scheme based on studies of cloned Drosophila G-protein coupled receptors. Invert. Neurosci. 5, 111-118.
11. Farooqui, T., Vaessin, H. and Smith, B. H. (2004). Octopamine receptors in the honeybee (Apis mellifera) brain and their disruption by RNA-mediated interference. J. Insect Physiol. 50, 701-713.
12. Fox, L. E., Soll, D. R. and Wu, C. F. (2006). Coordination and modulation of locomotion pattern generators in Drosophila larvae: effects of altered biogenic amine levels by the tyramine β hydroxlyase mutation. J. Neurosci. 26, 1486-1498.
13. Fussnecker, B. L., Smith, B. H. and Mustard, J. A. (2006). Octopamine and tyramine influence the behavioral profile of locomotor activity in the honey bee (Apis mellifera). J. Insect Physiol. 52, 1083-1092.
14. Grohmann, L., Blenau, W., Erber, J., Ebert, P. R., Strunker, T. and Baumann, A. (2003). Molecular and functional characterization of an octopamine receptor from honeybee (Apis mellifera) brain. J. Neurochem. 86, 725-735.
15. Han, K. A., Millar, N. S. and Davis, R. L. (1998). A novel octopamine receptor with preferential expression in Drosophila mushroom bodies. J. Neurosci. 18, 3650-3658.
16. Hoyer, S. C., Eckart, A., Herrel, A., Zars, T., Fischer, S. A., Hardie, S. L. and Heisenberg, M. (2008). Octopamine in male aggression of Drosophila. Curr. Biol. 18, 159-167.
17. Huang, J., Ohta, H., Inoue, N., Takao, H., Kita, T., Ozoe, F. and Ozoe, Y. (2009). Molecular cloning and pharmacological characterization of a Bombyx mori tyramine receptor selectively coupled to intracellular calcium mobilization. Insect Biochem. Mol. Biol. 39, 842-849.
18. Huang, J., Hamasaki, T. and Ozoe, Y. (2010). Pharmacological characterization of a Bombyx mori α-adrenergic-like octopamine receptor stably expressed in a mammalian cell line. Arch. Insect Biochem. Physiol. 73, 74-86.
19. Hui, X. M., Yang, L. W., He, G. L., Yang, Q. P., Han, Z. J. and Li, F. (2011). RNA interference of ace1 and ace2 in Chilo suppressalis reveals their different contributions to motor ability and larval growth. Insect Mol. Biol. 20, 507-518.
20. Koon, A. C., Ashley, J., Barria, R., DasGupta, S., Brain, R., Waddell, S., Alkema, M. J. and Budnik, V. (2011). Autoregulatory and paracrine control of synaptic and behavioral plasticity by octopaminergic signaling. Nat. Neurosci. 14, 190-199.
21. Lange, A. B. (2009). Tyramine: from octopamine precursor to neuroactive chemical in insects. Gen. Comp. Endocrinol. 162, 18-26.
22. Maqueira, B., Chatwin, H. and Evans, P. D. (2005). Identification and characterization of a novel family of Drosophila β-adrenergic-like octopamine G-protein coupled receptors. J. Neurochem. 94, 547-560.
23. Min, V. A. and Condron, B. G. (2005). An assay of behavioral plasticity in Drosophila larvae. J. Neurosci. Methods 145, 63-72.
24. Monastirioti, M., Linn, C. E., Jr and White, K. (1996). Characterization of Drosophila tyramine β-hydroxylase gene and isolation of mutant flies lacking octopamine. J. Neurosci. 16, 3900-3911.
25. Ohta, H., Utsumi, T. and Ozoe, Y. (2003). B96Bom encodes a Bombyx mori tyramine receptor negatively coupled to adenylate cyclase. Insect Mol. Biol. 12, 217-223.
26. Rillich, J., Schildberger, K. and Stevenson, P. A. (2011). Octopamine and occupancy: an aminergic mechanism for intruder-resident aggression in crickets. Proc. R. Soc. B 278, 1873-1880.
27. Roeder, T. (1999). Octopamine in invertebrates. Prog. Neurobiol. 59, 533-561.
28. Roeder, T. (2005). Tyramine and octopamine: ruling behavior and metabolism. Annu. Rev. Entomol. 50, 447-477.
29. Rotte, C., Krach, C., Balfanz, S., Baumann, A., Walz, B. and Blenau, W. (2009). Molecular characterization and localization of the first tyramine receptor of the American cockroach (Periplaneta americana). Neuroscience 162, 1120-1133.
30. Saraswati, S., Fox, L. E., Soll, D. R. and Wu, C. F. (2004). Tyramine and octopamine have opposite effects on the locomotion of Drosophila larvae. J. Neurobiol. 58, 425-441.
31. Saudou, F., Amlaiky, N., Plassat, J. L., Borrelli, E. and Hen, R. (1990). Cloning and characterization of a Drosophila tyramine receptor. EMBO J. 9, 3611-3617.
32. Shang, Z. Z., Wang, Y. S. and Zou, Y. H. (1979). Study on rearing method of rice stem borer Chilo suppressalis Walker. Acta Entomol. Sin. 22, 164-167.
33. Suo, S., Kimura, Y. and Van Tol, H. H. (2006). Starvation induces cAMP response element-binding protein-dependent gene expression through octopamine-Gq signaling in Caenorhabditis elegans. J. Neurosci. 26, 10082-10090.
34. Tamura, K., Dudley, J., Nei, M. and Kumar, S. (2007). MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) software version 4.0. Mol. Biol. Evol. 24, 1596-1599.
35. Verlinden, H., Vleugels, R., Marchal, E., Badisco, L., Pfluger, H. J., Blenau, W. and Broeck, J. V. (2010a). The role of octopamine in locusts and other arthropods. J. Insect Physiol. 56, 854-867.
36. Verlinden, H., Vleugels, R., Marchal, E., Badisco, L., Tobback, J., Pfluger, H. J., Blenau, W. and Vanden Broeck, J. (2010b). The cloning, phylogenetic relationship and distribution pattern of two new putative GPCR-type octopamine receptors in the desert locust (Schistocerca gregaria). J. Insect Physiol. 56, 868-875.
37. Zhou, C., Rao, Y. and Rao, Y. (2008). A subset of octopaminergic neurons are important for Drosophila aggression. Nat. Neurosci. 11, 1059-1067.