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Molecular cloning and expression of a rat Via arginine vasopressin receptor

Abstract

THE neurohypophyseal hormone arginine vasopressin has diverse actions1–7 , including the inhibition of diuresis, contraction of smooth muscle, stimulation of liver glycogenolysis and modulation of adrenocorticotropic hormone release from the pituitary. Arginine vasopressin receptors are G protein-coupled and have been divided into at least three types8; the Via (vascular/hepatic)1,9–11and Vlb (anterior pituitary)12 receptors which act through phosphatidylinositol hydrolysis to mobilize intracellular Ca2+, and the V2 (kidney) receptor1,13,14which is coupled to adenylate cyclase. We report here the cloning of a complementary DNA encoding the hepatic Via arginine vasopressin receptor. The liver cDNA encodes a protein with seven putative transmembrane domains, which binds arginine vasopressin and related compounds with affinities similar to the native rat Via receptor. The messenger RNA corresponding to the cDNA is distributed in rat tissues known to contain Via receptors.

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References

  1. Jard, S. Front. Hormont Res. 13, 89–104 (1985).

    Article  CAS  Google Scholar 

  2. van Ree, J. M., Bonus, B., Versteeg, D. H. G. & de Wied, D. Biochem. Pharmac. 27, 1793–1800 (1978).

    Article  CAS  Google Scholar 

  3. Gillies, G., Linton, E. A. & Lowry, P. J. Nature 299, 355–357 (1982).

    Article  ADS  CAS  Google Scholar 

  4. de Wied, D. Life Sci. 20, 192–294 (1977).

    Article  Google Scholar 

  5. Kasting, N. W., Veal, W. C. & Couper, K. E. Can. J. Physiol. Pharmac. 58, 316–319 (1980).

    Article  CAS  Google Scholar 

  6. Matsuguchi, H., Schmid, P. G., Gorden, F. J. & Johnson, A. K. Physiologist 23, 29–33 (1980).

    Google Scholar 

  7. Clements, J. A. & Funder, J. W. Endocr. Rev. 116, 416–423 (1986).

    Google Scholar 

  8. Michell, R. H., Kirk, C. J. & Billah, M. M. Biochem. Soc. Trans. 7, 861–865 (1979).

    Article  CAS  Google Scholar 

  9. Kirk, C. J., Verrinder, T. R. & Hems, D. A. FEBS Lett. 83, 267–271 (1977).

    Article  CAS  Google Scholar 

  10. Aiyar, N., Nambi, P., Stassen, F. L. & Crooke, S. J. Life Sci. 39, 37–45 (1986).

    Article  CAS  Google Scholar 

  11. Nambi, P., Whitman, M., Gessner, G., Aiyar, N. & Crooke, S. J. Proc. natn. Acad. Sci. U.S.A. 83, 8492–8495 (1986).

    Article  ADS  CAS  Google Scholar 

  12. Antoni, F. A. Neuroendocrinology 39, 186–188 (1984).

    Article  CAS  Google Scholar 

  13. Chase, L. R. & Aurbach, G. D. Science 159, 545–547 (1968).

    Article  ADS  CAS  Google Scholar 

  14. Butlen, D. et al. Molec. Pharmac. 14, 1006–1017 (1978).

    CAS  Google Scholar 

  15. Kozak, M. Nucleic Acids Res. 12, 857–872 (1984).

    Article  CAS  Google Scholar 

  16. Bunzow, J. R. et al. Nature 336, 783–787 (1988).

    Article  ADS  CAS  Google Scholar 

  17. Kozak, M. Nucleic Acids Res. 12, 857–872 (1984).

    Article  CAS  Google Scholar 

  18. Bunzow, J. R. et al. Nature 336, 783–787 (1988).

    Article  ADS  CAS  Google Scholar 

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

    Article  ADS  CAS  Google Scholar 

  20. Yokota, Y. et al. J. biol. Chem. 264, 17649–17652 (1989).

    CAS  Google Scholar 

  21. Arai, H., Hori, S., Aramori, I., Ohkubo, H. & Nakanishi, S. Nature 348, 730–732 (1990).

    Article  ADS  CAS  Google Scholar 

  22. Hirata, M. et al. Nature 349, 617–620 (1991).

    Article  ADS  CAS  Google Scholar 

  23. Matsuda, L. A., Lolait, S. J., Brownstein, M. J., Young, A. C. & Bonner, T. I. Nature 346, 561–564 (1990).

    Article  ADS  CAS  Google Scholar 

  24. Phillips, P. et al. Endocrinology 126, 1478–1484 (1990).

    Article  CAS  Google Scholar 

  25. Meidan, R. & Hsueh, A. J. W. Endocrinology 116, 416–423 (1985).

    Article  CAS  Google Scholar 

  26. Thibonnier, M., Snajdar, R. M. & Rapp, J. P. Am. J. Physiol. 251, 115–120 (1986).

    Article  Google Scholar 

  27. Woods, N. M., Cuthbertson, K. S. R. & Cobbold, P. H. Nature 319, 600–602 (1986).

    Article  ADS  CAS  Google Scholar 

  28. Chen, C. & Okayama, H. Molec. cell. Biol. 7, 2745–2752 (1987).

    Article  CAS  Google Scholar 

  29. Holmes, M. C., Antoni, F. A. & Szentendrei, T. Neuroendocrinology 39, 162–169 (1984).

    Article  CAS  Google Scholar 

  30. Antoni, F. A. Neuropeptides 4, 413–420 (1984).

    Article  CAS  Google Scholar 

  31. Balla, T., Enyedi, P., Spat, A. & Antoni, F. Endocrinology 117, 421–423 (1985).

    Article  CAS  Google Scholar 

  32. Okayama, H. et al. Meth. Enzym. 154, 3–28 (1987).

    Article  CAS  Google Scholar 

  33. Kimura, T., Tanizawa, O., Mori, K., Brownstein, M. J. & Okayama, H. Nature 356, 526–529 (1992).

    Article  ADS  CAS  Google Scholar 

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Morel, A., O'Carroll, AM., Brownstein, M. et al. Molecular cloning and expression of a rat Via arginine vasopressin receptor. Nature 356, 523–526 (1992). https://doi.org/10.1038/356523a0

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