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Cloning and expression of a rat D2 dopamine receptor cDNA

Abstract

Dopamine receptors are classified into D1 and D2 subtypes on the basis of their pharmacological and biochemical characteristics1,2. The D2 dopamine receptor has been implicated in the pathophysiology and treatment of movement disorders3, schizophrenia4 and drug addiction5. The D2 dopamine receptor interacts with guanine nucleotide-binding proteins to induce second messenger systems6,7. Other members of the family of receptors that are coupled to G proteins share a significant similarity in primary amino-acid sequence and exhibit an archetypical topology predicted to consist of seven putative transmembrane domains8. We have taken advantage of the expected nucleotide sequence similarities among members of this gene family to isolate genes coding for new receptors. Using the hamster β2-adrenergic receptor gene as a hybridization probe we have isolated related genes including a cDNA encoding the rat D2 dopamine receptor. This receptor has been characterized on the basis of three criteria: the deduced amino-acid sequence which reveals that it is a member of the family of G-protein-coupled receptors; the tissue distribution of the mRNA which parallels that of the D2 dopamine receptor; and the pharmacological profile of mouse fibroblast cells transfected with the cDNA.

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References

  1. Creese, I., Sibley, D. R., Hamblin, M. W. & Leff, S. E. A. Rev. Neurosci. 6, 43–71 (1983).

    Article  CAS  Google Scholar 

  2. Seeman, P. Pharmac. Rev. 32, 229–313 (1980).

    CAS  Google Scholar 

  3. Lee, T. et al. Nature 273, 59–61 (1984).

    Article  ADS  Google Scholar 

  4. Seeman, P. et al. Science 225, 728–731 (1984).

    Article  ADS  CAS  Google Scholar 

  5. Barnes, D. M. Science 241, 415–417 (1988).

    Article  ADS  CAS  Google Scholar 

  6. Cote, T. E., Frey, E. A., Grewe, C. W., & Kebabian, J. W. J. Neural. Trans. Suppl. 18, 139–147 (1983).

    CAS  Google Scholar 

  7. Senogles, S. E. et al. J. biol. Chem. 262, 4860–4867 (1987).

    CAS  PubMed  Google Scholar 

  8. Dohlman, H. G., Caron, M. G. & Lefkowitz, R. J. Biochemistry 26, 2657–2664 (1987).

    Article  CAS  Google Scholar 

  9. Dixon, R. A. F. et al. Nature 321, 75–79 (1986).

    Article  ADS  CAS  Google Scholar 

  10. Mount, S. M. Nucleic Acids Res. 10, 459–472 (1982).

    Article  CAS  Google Scholar 

  11. Grigoriadis, D. E., Niznik, H. B., Jarvie, K. R. & Seeman, P. FEBS Lett. 227, 220–224 (1988).

    Article  CAS  Google Scholar 

  12. Kobilka, B. K. et al. Science 238, 650–656 (1987).

    Article  ADS  CAS  Google Scholar 

  13. Kobilka, B. K. et al. Nature 329, 75–79 (1987).

    Article  ADS  CAS  Google Scholar 

  14. Kubo, T. et al. Nature 323, 411–416 (1986).

    Article  ADS  CAS  Google Scholar 

  15. Masu, Y. et al. Nature 329, 836–838 (1987).

    Article  ADS  CAS  Google Scholar 

  16. Strader, C. D. et al. J. biol. Chem. 263, 10267–10271 (1988).

    CAS  PubMed  Google Scholar 

  17. Sibley, D. R., Benovic, J. L., Caron, M. G. & Lefkowitz, R. J. Cell 48, 913–922 (1987).

    Article  CAS  Google Scholar 

  18. Bouvier, M. et al. Nature 333, 370–373 (1988).

    Article  ADS  CAS  Google Scholar 

  19. Boyson, S. J., McGonigle, P. & Molinott, P. B. J. Neurosci. 6, 3177–3188 (1986).

    Article  CAS  Google Scholar 

  20. Gorman, C., Padmanabhan, R. & Howard, B. H. Science 221, 551–553 (1983).

    Article  ADS  CAS  Google Scholar 

  21. Hamblin, M. W., Leff, S. E. & Creese, I. Biochem. Pharmac. 33, 872–877 (1984).

    Article  Google Scholar 

  22. Dolphin, A. C. Trends Neurosci. 10, 53–57 (1987).

    Article  CAS  Google Scholar 

  23. Jones, S. V. P. et al. Proc. natn. Acad. Sci. U.S.A 85, 4056–4060 (1988).

    Article  ADS  CAS  Google Scholar 

  24. Cheng, Y. C. & Prusoff, W. H. Biochem. Pharmac. 22, 3099–3108 (1973).

    Article  CAS  Google Scholar 

  25. Hyttel, J. Eur. J. Pharmac. 91, 153–154 (1983).

    Article  CAS  Google Scholar 

  26. Sanger, F., Nicklen, S. & Coulson, A. R. Proc. natn. Acad. Sci. U.S.A. 74, 5463–5467 (1977).

    Article  ADS  CAS  Google Scholar 

  27. Chirgwin, J. M., Przybyla, A. E., McDonald, R. J. & Rutter, W. J. Biochemistry 18, 5294–5299 (1979).

    Article  CAS  Google Scholar 

  28. Ullrich, A. et al. Science 196, 1313–1319 (1977).

    Article  ADS  CAS  Google Scholar 

  29. Uhler, M. & McKnight, G. S. J. biol. Chem. 262, 15202–15207 (1987).

    CAS  PubMed  Google Scholar 

  30. Neve, K. A. & Molinoff, P. B. Molec. Pharmac. 30, 104–111 (1986).

    CAS  Google Scholar 

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Bunzow, J., Tol, H., Grandy, D. et al. Cloning and expression of a rat D2 dopamine receptor cDNA. Nature 336, 783–787 (1988). https://doi.org/10.1038/336783a0

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