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Removal of phosphorylation sites from the β2-adrenergic receptor delays onset of agonist-promoted desensitization
- Michel Bouvier1,
- William P. Hausdorff1,
- Antonio De Blasi1,
- Brian F. O'Dowd1,
- Brian K. Kobilka1,
- Marc G. Caron1 &
- …
- Robert J. Lefkowitz1
Naturevolume 333, pages370–373 (1988)Cite this article
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Abstract
Eukaryotic cells have evolved a variety of mechanisms for dampening their responsiveness to hormonal stimulation in the face of sustained activation. The mechanisms for such processes, collectively referred to as desensitization, often involve alterations in the properties and number of cell-surface hormone receptors1–3. It has been speculated that phosphorylation–dephosphorylation reactions, which are known to regulate the catalytic activities of enzymes, also regulate the function of receptors4. Highly specific receptor kinases, such as rhodopsin kinase5 and β-adrenergic receptor kinase6, which show stimulus-dependent phosphorylation of receptors have been described. Direct evidence for a causal relationship between receptor phosphorylation and desensitization has been lacking however. Here we report that prevention of agonist-stimulated β2-adrenergic receptor (β2AR) phosphorylation by truncation of its serine and threonine-rich phosphate acceptor segment delays the onset of desensitization. We also show that selective replacement of these serine and theronine residues by alanine and glycine delays desensitization even further. These data provide the first direct evidence that one molecular mechanism of desensitization of G-protein-coupled receptors involves their agonist-induced phosphorylation.
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References
Harden, T. K.Pharmac. Rev.35, 5–23 (1983).
Clark, R. B.Adv. Cyclic Nucleotide Res.20, 155–209 (1986).
Sibley, D. R. & Lefkowitz, R. J.Nature317, 124–129 (1985).
Sibley, D. R., Benovic, J. L., Caron, M. G. & Lefkowitz, R. J.Cell48, 913–922 (1987).
Kuhn, H. & Dreyer, W. J.FFBS Lett.20, 1–6 (1972).
Benovic, J. L., Strasser, R. H., Caron, M. G. & Lefkowitz, R. J.Proc. natn. Acad. Sci. U.S.A.83, 2797–2801 (1986).
Dixon, R. A. F.et al.Nature321, 75–79 (1986).
Dohlman, H. G., Bouvier, M., Benovic, J. L., Caron, M. G. & Lefkowitz, R. J.J. biol. Chem.262, 14282–14288 (1987).
Henderson, R. & Umwin, P. N. T.Nature257, 28–32 (1975).
Hargrave, P. A.et al.Neurochem. Int.1, 231–244 (1980).
Thompson, P. & Findlay, J. B. C.Biochem. J.220, 773–780 (1984).
Miller, J. L. & Dratz, E. A.Vision Res.24, 1509–1521 (1984).
Bouvier, M.et al.Molec. Pharmac.33, 133–139 (1988).
Homburger, V.et al.J. biol. Chem.255, 10436–10444 (1980).
Waldo, G. L., Northup, A. J. K., Perkins, J. P. & Harden, T. K.J. biol. Chem.258, 13900–13908 (1983).
Strader, C. D.et al.Cell49, 855–863 (1987).
Benovic, J. L.et al.Proc. natn. Acad. Sci. U.S.A.24, 8879–8882 (1987).
Huganir, R. L., Delcour, A. H., Greengard, P. & Hess, G. P.Nature321, 774–776 (1986).
Kobilka, B. K.et al.J. biol. Chem.262, 7321–7327 (1987).
Cullen, B.Meth. Enzym.152, 684 (1987).
Gorman, C. inDNA cloning, A Practical Approach Vol.II. (ed. Glover, D. M.) 143–290 (IRL Press, Oxford, 1985).
Laemmli, U. K.Nature227, 680–686 (1970).
Shorr, R. G. L., Lefkowitz, R. J. & Caron, M. G.J. biol. Chem.256, 5820–5826 (1981).
Salomon, Y., Londos, C. & Rodbell, M.Analyt. Biochem.58, 541–548 (1974).
DeBlasi, A., Lipartiti, M., Motulsky, S., Insel, P. A. & Fratelli, M.J. clin. Endocr. Metab.61, 1081–1088 (1985).
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Authors and Affiliations
Howard Hughes Medical Institute Laboratories, Departments of Physiology, Medicine and Biochemistry, Duke University Medical Center, Durham, North Carolina, 27710, USA
Michel Bouvier, William P. Hausdorff, Antonio De Blasi, Brian F. O'Dowd, Brian K. Kobilka, Marc G. Caron & Robert J. Lefkowitz
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- William P. Hausdorff
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- Antonio De Blasi
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- Brian F. O'Dowd
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- Brian K. Kobilka
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- Marc G. Caron
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- Robert J. Lefkowitz
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Bouvier, M., Hausdorff, W., Blasi, A.et al. Removal of phosphorylation sites from the β2-adrenergic receptor delays onset of agonist-promoted desensitization.Nature333, 370–373 (1988). https://doi.org/10.1038/333370a0
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