Hormonal stimulation of adenylyl cyclase through Gi-protein βγ subunits (original) (raw)
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- Published: 12 March 1992
Nature volume 356, pages 159–161 (1992)Cite this article
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Abstract
AGONIST-BOUND receptors activate heterotrimeric (αβγ) G proteins by catalysing replacement by GTP of GDP bound to the a subunit, resulting in dissociation of α-GTP from the βγ subunits. In most cases, α-GTP carries the signal to effectors, as in hormonal stimulation1–4 and inhibition5,6of adenylyl cyclase by αs and αi, respectively. By contrast, genetic evidence in yeast7 and studies in mammalian cells8–10 suggest that βγ subunits of G proteins may also regulate effector pathways. Indeed, of the four recombinant mammalian adenylyl cyclases available for study11–14, two, adenylyl cyclases II and IV, are stimulated by βγ. This effect of βγ requires costimulation by αs-GTP14,15. This conditional pattern of effector responsiveness led to the prediction15 that receptors coupled to many G proteins will mediate elevation of cellular cyclic AMP, provided that Gs is also active. We now confirm this prediction. Coexpression of mutationally active αs with adenylyl cyclase II converted agonists that act through 'inhibitory' receptors (coupled to Gi) into stimulators of cAMP synthesis. Experiments using pertussis toxin and a putative scavenger ofβγ , the α subunit of transducin, suggest that βγ subunits of the Gi proteins mediated this stimulation. These findings assign a new signalling function to βγ subunits of Gi proteins, the conditional stimulation of cAMP synthesis by adenylyl cyclase II.
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References
- Birnbaumer, L. A. Rev. Pharmac. Tox. 30, 675–705 (1990).
Article CAS Google Scholar - Kaziro, Y., Itoh, H., Kozasa, T., Nakafuku, M. & Satoh, T. A. Rev. Biochem. 60, 349–400 (1991).
Article CAS Google Scholar - Bourne, H. R., Sanders, D. A. & McCormick, F. Nature 348, 125–132 (1990).
Article ADS CAS Google Scholar - Freissmuth, M., Casey, P. J. & Gilman, A. G. FASEB J. 3, 2125–2131 (1989).
Article CAS Google Scholar - Wong, Y. H. et al. Nature 351, 63–65 (1991).
Article ADS CAS Google Scholar - Wong, Y. H., Conklin, B. R. & Bourne, H. R. Science 255, 339–342 (1992).
Article ADS CAS Google Scholar - Whiteway, M., Hougan, L., Dignard, D., MacKay, V. & Thomas, D. Y. Cold Spring Harb. Symp. quant. Biol. 53, 585–590 (1988).
Article CAS Google Scholar - Logothetis, D. E., Kurachi, Y., Galper, J., Neer, E. J. & Clapham, D. E. Nature 325, 321–326 (1987).
Article ADS CAS Google Scholar - Jelsema, C. L. & Axelrod, J. Proc. natn. Acad. Sci. U.S.A. 84, 3623–3627 (1987).
Article ADS CAS Google Scholar - Kim, D. et al. Nature 337, 557–560 (1989).
Article ADS CAS Google Scholar - Krupinski, J. et al. Science 244, 1558–1564 (1989).
Article ADS CAS Google Scholar - Bakalyar, H. A. & Reed, R. R. Science 250, 1403–1406 (1990).
Article ADS CAS Google Scholar - Feinstein, P. G. et al. Proc. natn. Acad. Sci. U.S.A. 88, 10173–10177 (1991).
Article ADS CAS Google Scholar - Gao, B. & Gilman, A. G. Proc. natn. Acad. Sci. U.S.A. 88, 10178–10182 (1991).
Article ADS CAS Google Scholar - Tang, W.-J. & Gilman, A. G. Science 254, 1500–1503 (1991).
Article ADS CAS Google Scholar - Cotecchia, S. et al. J. biol. Chem. 265, 63–69 (1990).
CAS PubMed Google Scholar - Fraser, C. M., Arakawa, S., McCombie, W. R. & Venter, J. C. J. biol. Chem. 264, 11754–11761 (1989).
CAS PubMed Google Scholar - Grandy, D. K. et al. Proc. natn. Acad. Sci. U.S.A. 86, 9762–9766 (1989).
Article ADS CAS Google Scholar - Masters, S. B. et al. J. biol. Chem. 264, 15467–15474 (1989).
CAS Google Scholar - Medynski, D. C. et al. Proc. natn Acad. Sci U.S.A. 82, 4311–4315 (1985).
Article ADS CAS Google Scholar - Sattin, A., Rall, T. W. & Zanella, J. J. Pharmac. exp. Ther. 192, 22–32 (1975).
CAS Google Scholar - Daly, J. W. et al. J. Pharmac. exp. Ther. 212, 383–389 (1980).
Google Scholar - Karbon, E. W. & Enna, S. J. Molec. Pharmac. 27, 53–59 (1985).
CAS Google Scholar - Hill, D. R. Br. J. Pharmac. 84, 249–257 (1985).
CAS Google Scholar - Tang, W.-J., Krupinski, J. & Gilman, A. G. J. biol. Chem. 266, 8595–8603 (1991).
CAS PubMed Google Scholar - McFarland, K. C. et al. Science 245, 494–499 (1989).
Article ADS CAS Google Scholar - Guyer, C. A., et al. J. biol. Chem. 265, 17307–17317 (1990).
CAS Google Scholar - Salomon, Y., Londos, C. & Rodbell, M. Ana Biochem. 58, 541–548 (1974).
Article CAS Google Scholar - Mahan, L. C. et al. Molec. Pharmac. 40, 1–7 (1991).
CAS Google Scholar
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Authors and Affiliations
- Departments of Pharmacology and Medicine and the Cardiovascular Research Institute, University of California San Francisco, California, 94143, USA
Alex D. Federman, Bruce R. Conklin & Henry R. Bourne - Howard Hughes Medical Institute, Department of Molecular Biology and Genetics, Johns Hopkins School of Medicine, Baltimore, Maryland, 21205, USA
Karen A. Schrader & Randall R. Reed
Authors
- Alex D. Federman
You can also search for this author inPubMed Google Scholar - Bruce R. Conklin
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Federman, A., Conklin, B., Schrader, K. et al. Hormonal stimulation of adenylyl cyclase through Gi-protein βγ subunits.Nature 356, 159–161 (1992). https://doi.org/10.1038/356159a0
- Received: 07 November 1991
- Accepted: 23 December 1991
- Issue Date: 12 March 1992
- DOI: https://doi.org/10.1038/356159a0