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Activity-Dependent Internalization of Smoothened Mediated by ß-Arrestin 2 and GRK2
Wei Chen,1*Xiu-Rong Ren,2Christopher D. Nelson,2Larry S. Barak,3James K. Chen,4Philip A. Beachy,4Frederic de Sauvage,5Robert J. Lefkowitz2*
Binding of Sonic Hedgehog (Shh) to Patched (Ptc) relieves thelatter's tonic inhibition of Smoothened (Smo), a receptor thatspans the cell membrane seven times. This initiates signalingwhich, by unknown mechanisms, regulates vertebrate developmentalprocesses. We find that two molecules interact with mammalianSmo in an activation-dependent manner: G proteincoupledreceptor kinase 2 (GRK2) leads to phosphorylation of Smo, andß-arrestin 2 fused to green fluorescent protein interactswith Smo. These two processes promote endocytosis of Smo inclathrin-coated pits. Ptc inhibits association of ß-arrestin2 with Smo, and this inhibition is relieved in cells treatedwith Shh. A Smo agonist stimulated and a Smo antagonist (cyclopamine)inhibited both phosphorylation of Smo by GRK2 and interactionof ß-arrestin 2 with Smo. ß-Arrestin 2 andGRK2 are thus potential mediators of signaling by activatedSmo.
1 Department of Medicine, Duke University Medical Center, Durham, NC 27710, USA. 2 Howard Hughes Medical Institute, Departments of Medicine and Biochemistry, Duke University Medical Center, Durham, NC 27710, USA. 3 Department of Cell Biology, Duke University Medical Center, Durham, NC 27710, USA. 4 Howard Hughes Medical Institute, Department of Molecular Biology and Genetics, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA. 5 Department of Molecular Oncology, Genentech, South San Francisco, CA 94080, USA.
Present address: Department of Molecular Pharmacology, StanfordUniversity School of Medicine, Stanford, CA 94305, USA
* To whom correspondence should be addressed. E-mail: lefko001{at}receptor-biol.duke.edu (R.J.L.) and w.chen{at}duke.edu (W.C.).
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L. H.C. Van Lith, J. Oosterom, A. Van Elsas, and G. J.R. Zaman (2009)
J Biomol Screen
14, 1067-1075
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Converse Conformational Control of Smoothened Activity by Structurally Related Small Molecules.
H. Yang, J. Xiang, N. Wang, Y. Zhao, J. Hyman, S. Li, J. Jiang, J. K. Chen, Z. Yang, and S. Lin (2009)
J. Biol. Chem.
284, 20876-20884
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J. J. Kovacs, E. J. Whalen, R. Liu, K. Xiao, J. Kim, M. Chen, J. Wang, W. Chen, and R. J. Lefkowitz (2008)
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320, 1777-1781
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The G protein-coupled receptor regulatory kinase GPRK2 participates in Hedgehog signaling in Drosophila.
C. Molnar, H. Holguin, F. Mayor Jr., A. Ruiz-Gomez, and J. F. de Celis (2007)
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104, 7963-7968
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M. L. Oo, S. Thangada, M.-T. Wu, C. H. Liu, T. L. Macdonald, K. R. Lynch, C.-Y. Lin, and T. Hla (2007)
J. Biol. Chem.
282, 9082-9089
|Abstract »|Full Text »|PDF »
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Arrestin-2 and G Protein-coupled Receptor Kinase 5 Interact with NF{kappa}B1 p105 and Negatively Regulate Lipopolysaccharide-stimulated ERK1/2 Activation in Macrophages.
N. Parameswaran, C. S. Pao, K. S. Leonhard, D. S. Kang, M. Kratz, S. C. Ley, and J. L. Benovic (2006)
J. Biol. Chem.
281, 34159-34170
|Abstract »|Full Text »|PDF »
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S. J. Matkovich, A. Diwan, J. L. Klanke, D. J. Hammer, Y. Marreez, A. M. Odley, E. W. Brunskill, W. J. Koch, R. J. Schwartz, and G. W. Dorn II (2006)
Circ. Res.
99, 996-1003
|Abstract »|Full Text »|PDF »
Smoothened Signal Transduction Is Promoted by G Protein-Coupled Receptor Kinase 2.
A. R. Meloni, G. B. Fralish, P. Kelly, A. Salahpour, J. K. Chen, R. J. Wechsler-Reya, R. J. Lefkowitz, and M. G. Caron (2006)
Mol. Cell. Biol.
26, 7550-7560
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Human Receptors Patched and Smoothened Partially Transduce Hedgehog Signal When Expressed in Drosophila Cells.
M. De Rivoyre, L. Ruel, M. Varjosalo, A. Loubat, M. Bidet, P. Therond, and I. Mus-Veteau (2006)
J. Biol. Chem.
281, 28584-28595
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Activation of heterotrimeric G proteins by Smoothened.
N. A. Riobo, B. Saucy, C. DiLizio, and D. R. Manning (2006)
PNAS
103, 12607-12612
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S. Herranz, J. M. Rodriguez, H.-J. Bussink, J. C. Sanchez-Ferrero, H. N. Arst Jr., M. A. Penalva, and O. Vincent (2005)
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102, 12141-12146
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Loss of the Serine/Threonine Kinase Fused Results in Postnatal Growth Defects and Lethality Due to Progressive Hydrocephalus.
M. Merchant, M. Evangelista, S.-M. Luoh, G. D. Frantz, S. Chalasani, R. A. D. Carano, M. van Hoy, J. Ramirez, A. K. Ogasawara, L. M. McFarland, et al. (2005)
Mol. Cell. Biol.
25, 7054-7068
|Abstract »|Full Text »|PDF »
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