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Odorant signal termination by olfactory UDP glucuronosyl transferase

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Abstract

THE onset of olfactory transduction has been extensively studied1–7, but considerably less is known about the molecular basis of olfactory signal termination6,8,9. It has been suggested that the highly active cytochrome P450 monooxygenases of olfactory neuroepithelium10–12 are termination enzymes5,8,11,12, a notion supported by the identification and molecular cloning of olfactory-specific cytochrome P450s (refs. 13–16). But as reactions catalysed by cytochrome P450 (refs 17, 18) often do not significantly alter volatility, lipophilicity or odour properties9,11, cytochrome P450 may not be solely responsible for olfactory signal termination. In liver and other tissues, drug hydroxylation by cytochrome P450 is frequently followed by phase II biotransformation, for example by UDP glucuronosyl transferase (UGT), resulting in a major change of solubility and chemical properties19. We report here the molecular cloning and expression of an olfactory-specific UGT. The olfactory enzyme, but not the one in liver microsomes, shows preference for odorants over standard UGT substrates. Furthermore, glucuronic acid conjugation abolishes the ability of odorants1,20 to stimulate olfactory adenylyl cyclase. This, together with the known broad spectrum of drug-detoxification enzymes17,19, supports a role for olfactory UGT in terminating diverse odorant signals.

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References

  1. Pace, U., Hanski, E., Salomon, Y. & Lancet, D. Nature 316, 255–258 (1985).

    Article  ADS  CAS  Google Scholar 

  2. Sklar, P. B., Anholt, R. R. & Snyder, S. H. J. blol. Chem. 261, 15538–15543 (1986).

    CAS  Google Scholar 

  3. Shirley, S. G., Robinson, C. J., Dickinson, K., Aujla, R. & Dodd, G. H. Biochem. J. 240, 605–607 (1986).

    Article  CAS  Google Scholar 

  4. Lancet, D. & Pace, U. Trends biochem. Sci. 12, 63–66 (1987).

    Article  CAS  Google Scholar 

  5. Lancet, D., Lazard, D., Heldman, J., Khen, M. & Nef, P. Cold Spring Harbor Symp. quant. Biol. 53, 343–348 (1988).

    Article  CAS  Google Scholar 

  6. Snyder, S. H., Sklar, P. B., Hwang, P. M. & Pevsner, J. Trends Neurosci. 12, 35–38 (1989).

    Article  CAS  Google Scholar 

  7. Reed, R. R. Cell 60, 1–2 (1990).

    Article  CAS  Google Scholar 

  8. Getchell, T. V., Margolis, F. L. & Getchell, M. L. Prog. Neurobiol. 23, 317–345 (1984).

    Article  CAS  Google Scholar 

  9. Lancet, D. A. Rev. Neurosci. 9, 329–355 (1986).

    Article  CAS  Google Scholar 

  10. Dahl, A. R., Hadley, W. M., Hahn, F. F., Benson, J. M. & McClellan, R. O. Science 216, 57–59 (1982).

    Article  ADS  CAS  Google Scholar 

  11. Dahl, A. R. in Molecular Neurobiology of the Olfactory System (eds Margolis, F. L. & Getchell, T. V.) (Plenum, New York, 1988).

    Google Scholar 

  12. Jenner, J. & Dodd, G. H. Drug Metabol. Drug Interact. 6, 123–148 (1988).

    CAS  PubMed  Google Scholar 

  13. Nef, P. et al. J. biol. Chem. 264, 6780–6785 (1989).

    CAS  PubMed  Google Scholar 

  14. Ding, X. X. & Coon, M. J. Biochemistry 27, 8330–8337 (1988).

    Article  CAS  Google Scholar 

  15. Nef, P., Larabee, T. M., Kagimoto, K. & Meyer, U. A. J. biol. Chem. 265, 2903–2907 (1990).

    CAS  PubMed  Google Scholar 

  16. Lazard, D. et al. Biochemistry 29, 7433–7440 (1990).

    Article  CAS  Google Scholar 

  17. Black, S. D. & Coon, M. J. Adv. Enzym. 60, 35–87 (1987).

    CAS  Google Scholar 

  18. Nebert, D. W. & Gonzalez, F. J. A. Rev. Biochem. 56, 945–993 (1987).

    Article  CAS  Google Scholar 

  19. Burchell, B. & Coughtrie, M. W. Pharmac. Ther. 43, 261–289 (1989).

    Article  CAS  Google Scholar 

  20. Pace, U. & Lancet, D. Proc. natn. Acad. Sci. U.S.A. 83, 4947–4951 (1986).

    Article  ADS  CAS  Google Scholar 

  21. Mackenzie, P. I., Chowdhury, N. R. & Chowdhury, J. R. Clin. exp. pharmacol. Physiol. 16, 501–504 (1989).

    Article  CAS  Google Scholar 

  22. Pfeuffer, E., Mollner, S., Lancet, D. & Pfeuffer, T. J. biol. Chem. 264, 18803–18807 (1989).

    CAS  PubMed  Google Scholar 

  23. Fenaroli, G. Fenaroli's Handbook of Flavor Ingredients (eds Furia, E. T. & Bellanca, N.) (CRC, Cleveland, 1975).

    Google Scholar 

  24. Lazard, D., Barak, Y. & Lancet, D. Biochim. biophys. Acta 1013, 68–72 (1989).

    Article  CAS  Google Scholar 

  25. Voigt, J. M., Guengerich, F. P. & Baron, J. Cancer Lett. 27, 241–247 (1985).

    Article  CAS  Google Scholar 

  26. Foster, J. R. et al. Biochem. Pharmacol. 35, 4543–4554 (1986).

    Article  CAS  Google Scholar 

  27. Shepherd, S. R., Baird, S. J., Hallinan, T. & Burchell, B. Biochem. J. 259, 617–620 (1989).

    Article  CAS  Google Scholar 

  28. Crawford, J. M. & Gollan, J. L. Am. J. Physiol. 255, 121–131 (1988).

    Google Scholar 

  29. Gander, J. E. & Mannering, G. J. Pharmac. Ther. 10, 191–221 (1980).

    Article  CAS  Google Scholar 

  30. Shipley, M. T. Brain Res. Bull. 15, 129–142 (1985).

    Article  CAS  Google Scholar 

  31. Talamo, B. R. et al. Nature 337, 736–739 (1989).

    Article  ADS  CAS  Google Scholar 

  32. Wilbur, W. & Lipman, D. Proc. natn. Acad. Sci. U.S.A. 80, 726–730 (1983).

    Article  ADS  CAS  Google Scholar 

  33. Mackenzie, P. I. J. biol. Chem. 261, 6119–6125 (1986).

    CAS  PubMed  Google Scholar 

  34. Mackenzie, P. I. J. biol. Chem. 262, 9744–9749 (1987).

    CAS  PubMed  Google Scholar 

  35. Sompayrac, L. M. & Danna, K. J. Proc. natn. Acad. Sci. U.S.A. 78, 7575–7578 (1981).

    Article  ADS  CAS  Google Scholar 

  36. Graham, F. L. & Van der Eb, A. J. Virology 52, 456–467 (1973).

    Article  CAS  Google Scholar 

  37. Bansal, S. K. & Gessner, T. Analyt. Biochem. 109, 321–329 (1980).

    Article  CAS  Google Scholar 

  38. Salomon, Y., Londos, C. & Rodbell, M. Analyt. Biochem. 58, 541–548 (1974).

    Article  CAS  Google Scholar 

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Lazard, D., Zupko, K., Poria, Y. et al. Odorant signal termination by olfactory UDP glucuronosyl transferase. Nature 349, 790–793 (1991). https://doi.org/10.1038/349790a0

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