G-protein-coupled receptors, Hedgehog signaling and primary cilia
Open accessAbstract
The Hedgehog (Hh) pathway has become an important model to study the cell biology of primary cilia, and reciprocally, the study of ciliary processes provides an opportunity to solve longstanding mysteries in the mechanism of vertebrate Hh signal transduction. The cilium is emerging as an unique compartment for G-protein-coupled receptor (GPCR) signaling in many systems. Two members of the GPCR family, Smoothened and Gpr161, play important roles in the Hh pathway. We review the current understanding of how these proteins may function to regulate Hh signaling and also highlight some of the critical unanswered questions being tackled by the field. Uncovering GPCR-regulated mechanisms important in Hh signaling may provide therapeutic strategies against the Hh pathway that plays important roles in development, regeneration and cancer.
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Additional HH ligands, desert hedgehog and Indian hedgehog, also operate via primary cilia but in a tissue-specific manner, such as in testis cells and growth plate chondrocytes.
“Additional ligands of the HH family includes desert (DHH) and Indian (IHH) hedgehog, which also operate via primary cilia but in a tissue-specific manner, such as in cells of the testis and in growth plate chondrocytes 105, respectively.”
From Cellular signalling by primary cilia in development, organ function and disease (2019) · cites this paper as [105]
The Introduction (page not available) says vertebrate Hedgehog signaling depends on primary cilia and describes ciliary reception of Hedgehog ligands. It does not identify desert or Indian hedgehog or connect either ligand to testis cells or growth plate chondrocytes; searches for both ligand names found no such passage. (LLM, conf=0.84)
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1 retracted
Soetedjo, L., Glover, D. A., & Jin, H. (2013) · Biology Open · doi:10.1242/bio.20134747 · Cited by 17 · see citing works
RetractedCyclopia and defective axial patterning in mice lacking Sonic hedgehog gene function
Chiang, C. C., Litingtung, Y., Lee, E., Young, K. E., Corden, J. L., Westphal, H., & Beachy, P. A. (1996) · Nature · doi:10.1038/383407a0 · Cited by 3,062 · see citing works
The structure and function of G-protein-coupled receptors
Rosenbaum, D. M., Rasmussen, S. G. F., & Kobilka, B. K. (2009) · Nature · doi:10.1038/nature08144 · Cited by 2,534 · see citing works
Regulation of the Hedgehog and Wingless signalling pathways by the F-box/WD40-repeat protein Slimb
Jiang, J., & Struhl, G. (1998) · Nature · doi:10.1038/35154 · Cited by 1,735 · see citing works
Altered Neural Cell Fates and Medulloblastoma in Mouse <i>patched</i> Mutants
Goodrich, L. V., Milenković, L., Higgins, K. M., & Scott, M. P. (1997) · Science · doi:10.1126/science.277.5329.1109 · Cited by 1,696 · see citing works
Vertebrate Smoothened functions at the primary cilium
Corbit, K. C., Aanstad, P., Singla, V., Norman, A. R., Stainier, D. Y. R., & Reiter, J. F. (2005) · Nature · doi:10.1038/nature04117 · Cited by 1,481 · see citing works
Inhibition of Hedgehog signaling by direct binding of cyclopamine to SmoothenedPreprint
Chen, J., Taipale, J., Cooper, M. K., & Beachy, P. A. (2002) · Genes & Development · doi:10.1101/gad.1025302 · Cited by 1,464 · see citing works
Patched1 Regulates Hedgehog Signaling at the Primary Cilium
Rohatgi, R., Milenkovic, L., & Scott, M. P. (2007) · Science · doi:10.1126/science.1139740 · Cited by 1,426 · see citing works
Self-citationHedgehog signalling in the mouse requires intraflagellar transport proteins
Huangfu, D., Liu, A., Rakeman, A. S., Murcia, N. S., Niswander, L., & Anderson, K. V. (2003) · Nature · doi:10.1038/nature02061 · Cited by 1,425 · see citing works
Rosenbaum, J. L., & Witman, G. B. (2002) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm952 · Cited by 1,423 · see citing works
Nachury, M. V., Loktev, A. V., Zhang, Q., Westlake, C. J., Peränen, J., Merdes, A., Slusarski, D. C., Scheller, R. H., Bazan, J. F., Sheffield, V. C., et al. (2007) · Cell · doi:10.1016/j.cell.2007.03.053 · Cited by 1,384 · see citing works
Control of Neuronal Precursor Proliferation in the Cerebellum by Sonic Hedgehog
Wechsler‐Reya, R. J., & Scott, M. P. (1999) · Neuron · doi:10.1016/s0896-6273(00)80682-0 · Cited by 1,343 · see citing works
Effects of oncogenic mutations in Smoothened and Patched can be reversed by cyclopamine
Taipale, J., Chen, J., Cooper, M. K., Wang, B., Mann, R. K., Milenković, L., Scott, M. P., & Beachy, P. A. (2000) · Nature · doi:10.1038/35023008 · Cited by 1,314 · see citing works
Differential signal transduction by five splice variants of the PACAP receptor
Spengler, D., Waeber, C., Pantaloni, C., Holsboer, F., Bockaert, J., Seeburg, P. H., & Journot, L. (1993) · Nature · doi:10.1038/365170a0 · Cited by 1,182 · see citing works
AKAP signalling complexes: focal points in space and time
Wong, W., & Scott, J. D. (2004) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm1527 · Cited by 1,073 · see citing works
Wang, B., Fallon, J. F., & Beachy, P. A. (2000) · Cell · doi:10.1016/s0092-8674(00)80678-9 · Cited by 1,014 · see citing works
Small molecule modulation of Smoothened activity
Chen, J., Taipale, J., Young, K. E., Maiti, T., & Beachy, P. A. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.182542899 · Cited by 991 · see citing works
Haycraft, C. J., Banizs, B., Aydin-Son, Y., Zhang, Q., Michaud, E. J., & Yoder, B. K. (2005) · PLoS Genetics · doi:10.1371/journal.pgen.0010053 · Cited by 902 · see citing works
Structural basis of Wnt recognition by Frizzled
Janda, C. Y., Waghray, D., Levin, A. M., Thomas, C., & Garcia, K. (2012) · Science · doi:10.1126/science.1222879 · Cited by 880 · see citing works
Discrete Microdomains with High Concentration of cAMP in Stimulated Rat Neonatal Cardiac Myocytes
Zaccolo, M., & Pozzan, T. (2002) · Science · doi:10.1126/science.1069982 · Cited by 858 · see citing works
Teratogen-Mediated Inhibition of Target Tissue Response to <i>Shh</i> Signaling
Cooper, M. K., Porter, J. A., Young, K. E., & Beachy, P. A. (1998) · Science · doi:10.1126/science.280.5369.1603 · Cited by 848 · see citing works
Smoothened Mutation Confers Resistance to a Hedgehog Pathway Inhibitor in Medulloblastoma
Yauch, R. L., Dijkgraaf, G. J. P., Alicke, B., Januario, T., Ahn, C. P., Holcomb, T., Pujara, K., Stinson, J., Callahan, C. A., Tang, T. T.-L., et al. (2009) · Science · doi:10.1126/science.1179386 · Cited by 841 · see citing works
Cilia and Hedgehog responsiveness in the mouse
Huangfu, D., & Anderson, K. V. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0505328102 · Cited by 820 · see citing works
Patched acts catalytically to suppress the activity of Smoothened
Taipale, J., Cooper, M. K., Maiti, T., & Beachy, P. A. (2002) · Nature · doi:10.1038/nature00989 · Cited by 794 · cited 1× · see citing works
“This conclusion has been derived from the following observations: Ptch1 can inhibit Smo catalytically rather than stoichiometrically [16], Ptch1 and Smo do not physically interact in conventional biochemical assays, and Ptch1 demonstrates distant homology to the bacterial Resistance, Nodulation, Division (RND) family…”
BackgroundThe Dynamic Process of β2-Adrenergic Receptor Activation
Nygaard, R., Zou, Y., Dror, R. O., Mildorf, T. J., Arlow, D. H., Manglik, A., Pan, A. C., Liu, C. W., Fung, J. J., Bokoch, M. P., et al. (2013) · Cell · doi:10.1016/j.cell.2013.01.008 · Cited by 791 · see citing works
Dessaud, É., McMahon, A. P., & Briscoe, J. (2008) · Development · doi:10.1242/dev.009324 · Cited by 735 · see citing works
The teratogenic Veratrum alkaloid cyclopamine inhibits Sonic hedgehog signal transduction
Incardona, J. P., Gaffield, W., Kapur, R. P., & Roelink, H. (1998) · Development · doi:10.1242/dev.125.18.3553 · Cited by 654 · see citing works
Wallace, V. A. (1999) · Current Biology · doi:10.1016/s0960-9822(99)80195-x · Cited by 651 · see citing works
Seifert, R., & Wenzel‐Seifert, K. (2002) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-002-0588-0 · Cited by 638 · see citing works
Gli1 is a target of Sonic hedgehog that induces ventral neural tube development
Lee, J. D., Platt, K. A., Censullo, P., & Altaba, A. R. I. (1997) · Development · doi:10.1242/dev.124.13.2537 · Cited by 633 · see citing works
Interpretation of the sonic hedgehog morphogen gradient by a temporal adaptation mechanism
Dessaud, É., Yang, L. L., Hill, K., Cox, B., Ulloa, F., Ribeiro, A., Mynett, A., Novitch, B. G., & Briscoe, J. (2007) · Nature · doi:10.1038/nature06347 · Cited by 613 · see citing works
Lipidic cubic phase injector facilitates membrane protein serial femtosecond crystallography
Weierstall, U., James, D., Wang, C., White, T. A., Wang, D., Liu, W., Spence, J. C. H., Doak, R. B., Nelson, G., Fromme, P., et al. (2014) · Nature Communications · doi:10.1038/ncomms4309 · Cited by 584 · see citing works
Liu, A., Wang, B., & Niswander, L. A. (2005) · Development · doi:10.1242/dev.01894 · Cited by 536 · see citing works
Fantini, J., & Barrantes, F. J. (2013) · Frontiers in Physiology · doi:10.3389/fphys.2013.00031 · Cited by 532 · see citing works
Dynamic Association of Proteasomal Machinery with the Centrosome
Wigley, W. C., Fabunmi, R. P., Lee, M. G., Marino, C. R., Muallem, S., Demartino, G., & Thomas, P. (1999) · The Journal of Cell Biology · doi:10.1083/jcb.145.3.481 · Cited by 513 · see citing works
Arimura, A. (1998) · The Japanese Journal of Physiology · doi:10.2170/jjphysiol.48.301 · Cited by 512 · see citing works
Primary cilia are specialized calcium signalling organelles
Delling, M., DeCaen, P. G., Doerner, J. F., Febvay, S., & Clapham, D. E. (2013) · Nature · doi:10.1038/nature12833 · Cited by 497 · see citing works
Frank-Kamenetsky, M. D., Zhang, X. M., Bottega, S., Guicherit, O. M., Wichterle, H., Dudek, H., Bumcrot, D. A., Wang, F. Y., Jones, S. S., Shulok, J. R., et al. (2002) · Journal of Biology · doi:10.1186/1475-4924-1-10 · Cited by 488 · see citing works
Mukhopadhyay, S., Wen, X., Ratti, N., Loktev, A., Rangell, L., Scales, S. J., & Jackson, P. K. (2013) · Cell · doi:10.1016/j.cell.2012.12.026 · Cited by 486 · see citing works
Self-citationAssembly of allosteric macromolecular switches: lessons from PKA
Taylor, S. S., Ilouz, R., Zhang, P., & Kornev, A. P. (2012) · Nature Reviews Molecular Cell Biology · doi:10.1038/nrm3432 · Cited by 480 · see citing works
The Sonic Hedgehog-Gli pathway regulates dorsal brain growth and tumorigenesis
Dahmane, N., Sánchez‐Gómez, P., Gitton, Y., Palma, V., Sun, T., Beyna, M., Weiner, H. L., & Altaba, A. R. I. (2001) · Development · doi:10.1242/dev.128.24.5201 · Cited by 479 · see citing works
Mammalian Suppressor-of-Fused modulates nuclear–cytoplasmic shuttling of GLI-1
Kogerman, P., Grimm, T., Kogerman, L., Krause, D., Undén, A. B., Sandstedt, B., Toftgård, R., & Zaphiropoulos, P. G. (1999) · Nature Cell Biology · doi:10.1038/13031 · Cited by 476 · see citing works
Harmar, A. J., Fahrenkrug, J., Gozes, I., Laburthe, M., May, V., Pisegna, J. R., Vaudry, D., Vaudry, H., Waschek, J. A., & Said, S. I. (2012) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2012.01871.x · Cited by 472 · see citing works
Svärd, J., Henricson, K. H., Persson-Lek, M., Rozell, B., Lauth, M., Bergström, Å., Ericson, J., Toftgård, R., & Teglund, S. (2006) · Developmental Cell · doi:10.1016/j.devcel.2005.12.013 · Cited by 468 · see citing works
Balaskas, N., Ribeiro, A., Panovska, J., Dessaud, E., Sasai, N., Page, K., Briscoe, J., & Ribes, V. (2012) · Cell · doi:10.1016/j.cell.2011.10.047 · Cited by 468 · see citing works
Structure of the human smoothened receptor bound to an antitumour agent
Wang, C., Wu, H., Katritch, V., Han, G. W., Huang, X., Liu, W., Siu, F., Roth, B. L., Cherezov, V., & Stevens, R. C. (2013) · Nature · doi:10.1038/nature12167 · Cited by 465 · see citing works
Yamada, T., Pfaff, S. L., Edlund, H., & Jessell, T. M. (1993) · Cell · doi:10.1016/0092-8674(93)90248-o · Cited by 464 · see citing works
Primary cilia can both mediate and suppress Hedgehog pathway–dependent tumorigenesis
Wong, S. Y., Seol, A. D., So, P.-L., Ermilov, A. N., Bichakjian, C. K., Epstein, E. H., Dlugosz, A. A., & Reiter, J. F. (2009) · Nature Medicine · doi:10.1038/nm.2011 · Cited by 463 · see citing works
Humke, E. W., Dorn, K. V., Milenkovic, L., Scott, M. P., & Rohatgi, R. (2010) · Genes & Development · doi:10.1101/gad.1902910 · Cited by 444 · see citing works
Self-citationMukhopadhyay, S., Wen, X., Chih, B., Nelson, C. D., Lane, W. S., Scales, S. J., & Jackson, P. K. (2010) · Genes & Development · doi:10.1101/gad.1966210 · Cited by 435 · see citing works
Self-citationDual and opposing roles of primary cilia in medulloblastoma development
Han, Y.-G., Kim, H. J., Dlugosz, A. A., Ellison, D. W., Gilbertson, R. J., & Álvarez-Buylla, A. (2009) · Nature Medicine · doi:10.1038/nm.2020 · Cited by 406 · see citing works
Small-molecule inhibitors of the AAA+ ATPase motor cytoplasmic dynein
Firestone, A. J., Weinger, J. S., Maldonado, M., Barlan, K., Langston, L. D., O’Donnell, M., Gelfand, V. I., Kapoor, T. M., & Chen, J. K. (2012) · Nature · doi:10.1038/nature10936 · Cited by 403 · see citing works
Litingtung, Y., & Chiang, C. C. (2000) · Nature Neuroscience · doi:10.1038/79916 · Cited by 392 · see citing works
A defective response to Hedgehog signaling in disorders of cholesterol biosynthesis
Cooper, M. K., Wassif, C. A., Krakowiak, P. A., Taipale, J., Gong, R., Kelley, R. I., Porter, F. D., & Beachy, P. A. (2003) · Nature Genetics · doi:10.1038/ng1134 · Cited by 390 · see citing works
Tukachinsky, H., Lopez, L. V., & Salic, A. N. (2010) · The Journal of Cell Biology · doi:10.1083/jcb.201004108 · Cited by 388 · see citing works
Scheer, A., Fanelli, F., Costa, T., Benedetti, P. G. D., & Cotecchia, S. (1996) · The EMBO Journal · doi:10.1002/j.1460-2075.1996.tb00726.x · Cited by 386 · see citing works
Protein kinase A is a common negative regulator of Hedgehog signaling in the vertebrate embryo.Preprint
Hammerschmidt, M., Bitgood, M. J., & McMahon, A. (1996) · Genes & Development · doi:10.1101/gad.10.6.647 · Cited by 352 · see citing works
Kim, J., Kato, M., & Beachy, P. A. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0912180106 · Cited by 347 · see citing works
Transmembrane molecular pump activity of Niemann-Pick C1 protein.
Davies, J. P., Chen, F.-N. W., & Ioannou, Y. (2000) · Science · doi:10.1126/science.290.5500.2295 · Cited by 346 · see citing works
Tran, P. V., Haycraft, C. J., Besschetnova, T. Y., Turbé-Doan, A., Stottmann, R. W., Herron, B. J., Chesebro, A. L., Qiu, H., Scherz, P., Shah, J. V., et al. (2008) · Nature Genetics · doi:10.1038/ng.105 · Cited by 337 · see citing works
Graded sonic hedgehog signaling and the specification of cell fate in the ventral neural tube.Preprint
Ericson, J., Briscoe, J., Rashbass, P., van Heyningen, V., & Jessell, T. M. (1997) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.1997.062.01.053 · Cited by 326 · see citing works
Oxysterols stimulate Sonic hedgehog signal transduction and proliferation of medulloblastoma cells
Corcoran, R. B., & Scott, M. P. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0602852103 · Cited by 314 · see citing works
Repression of Smoothened by Patched-Dependent (Pro-)Vitamin D3 Secretion
Bijlsma, M. F., Spek, C. A., Živković, D., van de Water, S., Rezaee, F., & Peppelenbosch, M. P. (2006) · PLoS Biology · doi:10.1371/journal.pbio.0040232 · Cited by 314 · see citing works
Direct recording and molecular identification of the calcium channel of primary cilia
DeCaen, P. G., Delling, M., Vien, T. N., & Clapham, D. E. (2013) · Nature · doi:10.1038/nature12832 · Cited by 306 · see citing works
Small-molecule inhibitors reveal multiple strategies for Hedgehog pathway blockade
Hyman, J. M., Firestone, A. J., Heine, V. M., Zhao, Y., Ocasio, C. A., Han, K., Sun, M., Rack, P. G., Sinha, S., Wu, J. J., et al. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0907134106 · Cited by 306 · see citing works
Mouse Kif7/Costal2 is a cilia-associated protein that regulates Sonic hedgehog signaling
Liem, K. F., He, M., Ocbina, P. J. R., & Anderson, K. V. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0906944106 · Cited by 300 · see citing works
Oxysterols Are Novel Activators of the Hedgehog Signaling Pathway in Pluripotent Mesenchymal Cells
Dwyer, J. R., Sever, N., Carlson, M. R. J., Nelson, S. F., Beachy, P. A., & Parhami, F. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m611741200 · Cited by 300 · see citing works
Klein, R. S., Rubin, J. B., Gibson, H. D., DeHaan, E. N., Alvarez-Hernandez, X., Segal, R. A., & Luster, A. D. (2001) · Development · doi:10.1242/dev.128.11.1971 · Cited by 295 · see citing works
Gli1can rescue the in vivo function ofGli2
Bai, C. B., & Joyner, A. L. (2001) · Development · doi:10.1242/dev.128.24.5161 · Cited by 291 · see citing works
Allen, B. L., Song, J. Y., Izzi, L., Althaus, I. W., Kang, J.-S., Charron, F., Krauss, R. S., & McMahon, A. P. (2011) · Developmental Cell · doi:10.1016/j.devcel.2011.04.018 · Cited by 285 · see citing works
Oxysterols are allosteric activators of the oncoprotein Smoothened
Nachtergaele, S., Mydock, L. K., Krishnan, K., Rammohan, J., Schlesinger, P. H., Covey, D. F., & Rohatgi, R. (2012) · Nature Chemical Biology · doi:10.1038/nchembio.765 · Cited by 284 · see citing works
Self-citationHedgehog signal transduction by Smoothened: Pharmacologic evidence for a 2-step activation process
Rohatgi, R., Milenković, L., Corcoran, R. B., & Scott, M. P. (2009) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0813373106 · Cited by 280 · see citing works
Self-citationβ-Arrestin–Mediated Localization of Smoothened to the Primary Cilium
Kovacs, J. J., Whalen, E. J., Liu, R., Xiao, K., Kim, J., Chen, M., Wang, J., Chen, W., & Lefkowitz, R. J. (2008) · Science · doi:10.1126/science.1157983 · Cited by 275 · see citing works
Proteomic Analysis of Mammalian Primary Cilia
Ishikawa, H., Thompson, J., Yates, J. R., & Marshall, W. F. (2012) · Current Biology · doi:10.1016/j.cub.2012.01.031 · Cited by 275 · see citing works
Hedgehog regulates smoothened activity by inducing a conformational switch
Zhao, Y., Tong, C., & Jiang, J. (2007) · Nature · doi:10.1038/nature06225 · Cited by 274 · see citing works
Wen, X., Lai, C. K., Evangelista, M., Hongo, J.-A. S., de Sauvage, F. J., & Scales, S. J. (2010) · Molecular and Cellular Biology · doi:10.1128/mcb.01089-09 · Cited by 257 · see citing works
Endoh‐Yamagami, S., Evangelista, M., Wilson, D. G., Wen, X., Theunissen, J.-W. F., Phamluong, K., Davis, M., Scales, S. J., Solloway, M. J., de Sauvage, F. J., et al. (2009) · Current Biology · doi:10.1016/j.cub.2009.06.046 · Cited by 256 · see citing works
The SCFSlimb ubiquitin ligase regulates Plk4/Sak levels to block centriole reduplication
Rogers, G. C., Rusan, N. M., Roberts, D. M., Peifer, M. A., & Rogers, S. L. (2009) · The Journal of Cell Biology · doi:10.1083/jcb.200808049 · Cited by 250 · see citing works
Cheung, H. O.-L., Zhang, X., Ribeiro, A., Mo, R., Makino, S., Puviindran, V., Law, K. K. L., Briscoe, J., & Hui, C. (2009) · Science Signaling · doi:10.1126/scisignal.2000405 · Cited by 249 · see citing works
Tempé, D., Casas, M., Karaz, S., Blanchet-Tournier, M.-F., & Concordet, J.-P. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.02183-05 · Cited by 249 · see citing works
Lum, L., Zhang, C., Oh, S., Mann, R. K., von Kessler, D. P., Taipale, J., Weis‐Garcia, F., Gong, R., Wang, B., & Beachy, P. A. (2003) · Molecular Cell · doi:10.1016/s1097-2765(03)00426-x · Cited by 245 · see citing works
Activation of heterotrimeric G proteins by Smoothened
Galdo, N. A. R., Saucy, B., DiLizio, C., & Manning, D. R. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0600880103 · Cited by 244 · see citing works
Gli Protein Activity Is Controlled by Multisite Phosphorylation in Vertebrate Hedgehog Signaling
Niewiadomski, P., Kong, J. H., Ahrends, R., Ma, Y., Humke, E. W., Khan, S., Teruel, M. N., Novitch, B. G., & Rohatgi, R. (2014) · Cell Reports · doi:10.1016/j.celrep.2013.12.003 · Cited by 239 · see citing works
Self-citationIzzi, L., Lévesque, M., Morin, S., Laniel, D., Wilkes, B. C., Mille, F., Krauss, R. S., McMahon, A. P., Allen, B. L., & Charron, F. (2011) · Developmental Cell · doi:10.1016/j.devcel.2011.04.017 · Cited by 237 · see citing works
GLI activation by atypical protein kinase C ι/λ regulates the growth of basal cell carcinomas
Atwood, S. X., Covington, M. L., Lee, A. G., Tang, J. Y., & Oro, A. E. (2013) · Nature · doi:10.1038/nature11889 · Cited by 236 · see citing works
Chen, Y., Sasai, N., Ma, G., Yue, T., Jia, J., Briscoe, J., & Jiang, J. (2011) · PLoS Biology · doi:10.1371/journal.pbio.1001083 · Cited by 225 · see citing works
Activation of Hedgehog signaling by loss of GNAS causes heterotopic ossification
Regard, J. B., Malhotra, D., Gvozdenovic‐Jeremic, J., Josey, M., Chen, M., Weinstein, L. S., Lü, J., Shore, E. M., Kaplan, F. S., & Yang, Y. (2013) · Nature Medicine · doi:10.1038/nm.3314 · Cited by 224 · see citing works
IFT25 Links the Signal-Dependent Movement of Hedgehog Components to Intraflagellar Transport
Keady, B. T., Samtani, R., Tobita, K., Tsuchya, M., San Agustin, J. T., Follit, J. A., Jonassen, J. A., Subramanian, R., Lo, C. W., & Pazour, G. J. (2012) · Developmental Cell · doi:10.1016/j.devcel.2012.04.009 · Cited by 216 · see citing works
The IFT-A complex regulates Shh signaling through cilia structure and membrane protein trafficking
Liem, K. F., Ashe, A., He, M., Satir, P., Moran, J., Beier, D., Wicking, C., & Anderson, K. V. (2012) · Journal of Cell Biology · doi:10.1083/jcb.201110049 · Cited by 214 · see citing works
Oxysterol binding to the extracellular domain of Smoothened in Hedgehog signaling
Nedelcu, D., Liu, J., Xu, Y., Jao, C. Y., & Salic, A. N. (2013) · Nature Chemical Biology · doi:10.1038/nchembio.1290 · Cited by 213 · see citing works
Wang, C., Pan, Y., & Wang, B. (2010) · Development · doi:10.1242/dev.052126 · Cited by 212 · see citing works
Complex interactions between genes controlling trafficking in primary cilia
Ocbina, P. J. R., Eggenschwiler, J. T., Moskowitz, I., & Anderson, K. V. (2011) · Nature Genetics · doi:10.1038/ng.832 · Cited by 208 · see citing works
A Novel Protein LZTFL1 Regulates Ciliary Trafficking of the BBSome and Smoothened
Seo, S., Zhang, Q., Bugge, K., Breslow, D. K., Searby, C. C., Nachury, M. V., & Sheffield, V. C. (2011) · PLoS Genetics · doi:10.1371/journal.pgen.1002358 · Cited by 205 · see citing works
Chizhikov, V. V., Davenport, J., Zhang, Q., Shih, E. K., Cabello, O. A., Fuchs, J. L., Yoder, B. K., & Millen, K. J. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.5586-06.2007 · Cited by 204 · see citing works
G protein Gαi functions immediately downstream of Smoothened in Hedgehog signalling
Ogden, S. K., Fei, D. L., Schilling, N. S., Ahmed, Y. F., Hwa, J., & Robbins, D. J. (2008) · Nature · doi:10.1038/nature07459 · Cited by 201 · see citing works
Myers, B. R., Sever, N., Chong, Y. C., Kim, J., Belani, J. D., Rychnovsky, S. D., Bazán, J. F., & Beachy, P. A. (2013) · Developmental Cell · doi:10.1016/j.devcel.2013.07.015 · Cited by 200 · see citing works
Ocbina, P. J. R., & Anderson, K. V. (2008) · Developmental Dynamics · doi:10.1002/dvdy.21551 · Cited by 192 · see citing works
Tuson, M., He, M., & Anderson, K. V. (2011) · Development · doi:10.1242/dev.070805 · Cited by 192 · see citing works
Stone, D. M., Murone, M., Luoh, S.-M., Ye, W., Armanini, M. P., Gurney, A. L., PHILLIPS, H. S., Brush, J., Goddard, A. D., de Sauvage, F. J., et al. (1999) · Journal of Cell Science · doi:10.1242/jcs.112.23.4437 · Cited by 191 · see citing works
Qin, J., Lin, Y., Norman, R. X., Ko, H. W., & Eggenschwiler, J. T. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1011410108 · Cited by 176 · see citing works
Specified Neural Progenitors Sort to Form Sharp Domains after Noisy Shh Signaling
Xiong, F., Tentner, A. R., Huang, P., Gelas, A., Mosaliganti, K. R., Souhait, L., Rannou, N., Swinburne, I. A., Obholzer, N. D., Cowgill, P. D., et al. (2013) · Cell · doi:10.1016/j.cell.2013.03.023 · Cited by 174 · see citing works
A Smoothened-Evc2 Complex Transduces the Hedgehog Signal at Primary Cilia
Dorn, K. V., Hughes, C. E., & Rohatgi, R. (2012) · Developmental Cell · doi:10.1016/j.devcel.2012.07.004 · Cited by 174 · see citing works
Self-citationActivity and Regulation of the Centrosome-associated Proteasome
Fabunmi, R. P., Wigley, W. C., Thomas, P., & Demartino, G. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.1.409 · Cited by 173 · see citing works
Structure and function of the Smoothened extracellular domain in vertebrate Hedgehog signaling
Nachtergaele, S., Whalen, D. M., Mydock, L. K., Zhao, Z., Malinauskas, T., Krishnan, K., Ingham, P. W., Covey, D. F., Siebold, C., & Rohatgi, R. (2013) · eLife · doi:10.7554/elife.01340 · Cited by 167 · see citing works
Self-citationAgonist-independent regulation of constitutively active G-protein-coupled receptors
Leurs, R., Smit, M. J., Alewijnse, A. E., & Timmerman, H. (1998) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(98)01287-0 · Cited by 156 · see citing works
Pan, Y., & Wang, B. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m608599200 · Cited by 152 · see citing works
BBS proteins interact genetically with the IFT pathway to influence SHH-related phenotypes
Zhang, Q., Seo, S., Bugge, K., Stone, E. M., & Sheffield, V. C. (2012) · Human Molecular Genetics · doi:10.1093/hmg/dds004 · Cited by 144 · see citing works
Choi, Y.-H., Suzuki, A., Hajarnis, S., Ma, Z., Chapin, H. C., Caplan, M. J., Pontoglio, M., Somlo, S., & Igarashi, P. (2011) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1016214108 · Cited by 139 · see citing works
MIM and Cortactin Antagonism Regulates Ciliogenesis and Hedgehog Signaling
Bershteyn, M., Atwood, S. X., Woo, W., Covington, M. L., & Oro, A. E. (2010) · Developmental Cell · doi:10.1016/j.devcel.2010.07.009 · Cited by 137 · see citing works
Suppressor of Fused inhibits mammalian Hedgehog signaling in the absence of cilia
Jia, J., Kolterud, Å., Zeng, H., Hoover, A., Teglund, S., Toftgård, R., & Liu, A. (2009) · Developmental Biology · doi:10.1016/j.ydbio.2009.04.009 · Cited by 132 · see citing works
Smoothened Signal Transduction Is Promoted by G Protein-Coupled Receptor Kinase 2
Meloni, A. R., Fralish, G. B., Kelly, P., Salahpour, A., Chen, J., Wechsler‐Reya, R. J., Lefkowitz, R. J., & Caron, M. G. (2006) · Molecular and Cellular Biology · doi:10.1128/mcb.00546-06 · Cited by 121 · see citing works
Nicot, A. B., Lelièvre, V., Tam, J., Waschek, J. A., & DiCicco-Bloom, E. M. (2002) · Journal of Neuroscience · doi:10.1523/jneurosci.22-21-09244.2002 · Cited by 120 · see citing works
Behal, R. H., Miller, M. S., Qin, H., Lucker, B. F., Jones, A., & Cole, D. G. (2012) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.287102 · Cited by 119 · see citing works
Ogden, S. K., Ascano, M., Stegman, M. A., Suber, L. M., Hooper, J. E., & Robbins, D. J. (2003) · Current Biology · doi:10.1016/j.cub.2003.10.004 · Cited by 117 · see citing works
Chen, M.-H., Gao, N., Kawakami, T., & Chuang, P. (2005) · Molecular and Cellular Biology · doi:10.1128/mcb.25.16.7042-7053.2005 · Cited by 116 · see citing works
Ruiz‐Pérez, V. L., & Goodship, J. A. (2009) · American Journal of Medical Genetics Part C Seminars in Medical Genetics · doi:10.1002/ajmg.c.30226 · Cited by 114 · see citing works
Chen, Y., Yue, S., Xie, L., Pu, X., Jin, T., & Cheng, S. Y. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.217604 · Cited by 113 · see citing works
Caparros-Martin, J. A., Valencia, M., Reytor, E., Pacheco, M., Fernández, M., Aytés, A. P., Geán, E., Lapunzina, P. D., Peters, H., Goodship, J. A., et al. (2012) · Human Molecular Genetics · doi:10.1093/hmg/dds409 · Cited by 111 · see citing works
Intraflagellar transport complex structure and cargo interactions
Bhogaraju, S., Engel, B. D., & Lorentzen, E. (2013) · Cilia · doi:10.1186/2046-2530-2-10 · Cited by 111 · see citing works
Smoothened transduces Hedgehog signal by forming a complex with Evc/Evc2
Yang, C., Chen, W., Chen, Y., & Jiang, J. (2012) · Cell Research · doi:10.1038/cr.2012.134 · Cited by 110 · see citing works
Protein Kinase A Deficiency Causes Axially Localized Neural Tube Defects in Mice
Huang, Y., Roelink, H., & McKnight, G. S. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m111412200 · Cited by 106 · see citing works
Regulation of neuroblast mitosis is determined by PACAP receptor isoform expression
Nicot, A. B., & DiCicco-Bloom, E. M. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.071465398 · Cited by 106 · see citing works
Norman, R. X., Ko, H. W., Huang, V., Eun, C. M., Abler, L. L., Zhang, Z., Sun, X., & Eggenschwiler, J. T. (2009) · Human Molecular Genetics · doi:10.1093/hmg/ddp113 · Cited by 103 · see citing works
Patterson, V. L., Damrau, C., Paudyal, A., Reeve, B., Grimes, D. T., Stewart, M. E., Williams, D. J., Siggers, P., Greenfield, A., & Murdoch, J. N. (2009) · Human Molecular Genetics · doi:10.1093/hmg/ddp075 · Cited by 101 · see citing works
Incardona, J. P., Gaffield, W., Lange, Y., Cooney, A. M., Pentchev, P. G., Liu, S., Watson, J. A., Kapur, R. P., & Roelink, H. (2000) · Developmental Biology · doi:10.1006/dbio.2000.9775 · Cited by 98 · see citing works
Tay, S. Y., Ingham, P. W., & Roy, S. (2005) · Development · doi:10.1242/dev.01606 · Cited by 92 · see citing works
Sonic-hedgehog-mediated proliferation requires the localization of PKA to the cilium base
Barzi, M., Berenguer, J., Menéndez, A., Álvarez-Rodríguez, R., & Pons, S. (2009) · Journal of Cell Science · doi:10.1242/jcs.060020 · Cited by 90 · see citing works
Pusapati, G. V., Hughes, C. E., Dorn, K. V., Zhang, D., Sugianto, P., Aravind, L., & Rohatgi, R. (2014) · Developmental Cell · doi:10.1016/j.devcel.2014.01.021 · Cited by 88 · see citing works
Self-citationStructural insights into the role of the Smoothened cysteine-rich domain in Hedgehog signalling
Rana, R., Carroll, C. E., Lee, H., Bao, J., Marada, S., Grace, C. R., Guibao, C. D., Ogden, S. K., & Zheng, J. (2013) · Nature Communications · doi:10.1038/ncomms3965 · Cited by 82 · see citing works
Mutational and Computational Analysis of the α1b-Adrenergic Receptor
Greasley, P. J., Fanelli, F., Scheer, A., Abuin, L., Nenniger-Tosato, M., Benedetti, P. G. D., & Cotecchia, S. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m105791200 · Cited by 75 · see citing works
Glucocorticoid Compounds Modify Smoothened Localization and Hedgehog Pathway Activity
Wang, Y., Davidow, L. S., Arvanites, A. C., Blanchard, J., Lam, K., Xu, K., Oza, V., Yoo, J. W., Ng, J. M. Y., Curran, T., et al. (2012) · Chemistry & Biology · doi:10.1016/j.chembiol.2012.06.012 · Cited by 73 · see citing works
Chen, Yön, Yue, Y., Shen, Xie, LU, L., Pu, P., Xiaohong, Jin, Tion, et al. (2011) · Acta Scientiarum Naturalium Universitatis Sunyatseni · Cited by 73 · see citing works
GPR88 Reveals a Discrete Function of Primary Cilia as Selective Insulators of GPCR Cross-Talk
Marley, A., Choy, R., & von Zastrow, M. (2013) · PLoS ONE · doi:10.1371/journal.pone.0070857 · Cited by 72 · see citing works
Smoothened Is a Fully Competent Activator of the Heterotrimeric G Protein Gi
Shen, F., Cheng, L., Douglas, A. E., Galdo, N. A. R., & Manning, D. R. (2013) · Molecular Pharmacology · doi:10.1124/mol.112.082511 · Cited by 71 · see citing works
Interaction of PACAP with Sonic hedgehog reveals complex regulation of the Hedgehog pathway by PKA
Niewiadomski, P., Zhujiang, A., Youssef, M., & Waschek, J. A. (2013) · Cellular Signalling · doi:10.1016/j.cellsig.2013.07.012 · Cited by 65 · see citing works
Matteson, P. G., Desai, J. S., Korstanje, R., Lazar, G., Borsuk, T. E., Rollins, J. A., Kadambi, S. M., Joseph, J., Rahman, T., Wink, J., et al. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0705657105 · Cited by 65 · see citing works
Low, W.-C., Wang, C., Pan, Y., Huang, X., Chen, J., & Wang, B. (2008) · Developmental Biology · doi:10.1016/j.ydbio.2008.06.014 · Cited by 62 · see citing works
Valencia, M., Lapunzina, P. D., Lim, D., Zannolli, R., Bartholdi, D., Wollnik, B., Al-Ajlouni, O., Eid, S. S., Cox, H., Buoni, S., et al. (2009) · Human Mutation · doi:10.1002/humu.21117 · Cited by 61 · see citing works
Small molecule inhibitors of Smoothened ciliary localization and ciliogenesis
Wu, V., Chen, S. C., Arkin, M. R., & Reiter, J. F. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1207170109 · Cited by 56 · see citing works
Disruption of the PACAP gene promotes medulloblastoma in ptc1 mutant mice
Lelièvre, V., Seksenyan, A., Nobuta, H., Yong, W. H., Chhith, S., Niewiadomski, P., Cohen, J. R., Dong, H., Flores, A., Liau, L. M., et al. (2007) · Developmental Biology · doi:10.1016/j.ydbio.2007.10.031 · Cited by 50 · see citing works
Wang, Y., Arvanites, A. C., Davidow, L. S., Blanchard, J., Lam, K., Yoo, J. W., Coy, S., Rubin, L. L., & McMahon, A. P. (2012) · ACS Chemical Biology · doi:10.1021/cb300028a · Cited by 44 · see citing works
A Three-part Signal Governs Differential Processing of Gli1 and Gli3 Proteins by the Proteasome
Schrader, E. K., Harstad, K. G., Holmgren, R. A., & Matouschek, A. T. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.274993 · Cited by 37 · see citing works
Interaction of smoothened with integrin‐linked kinase in primary cilia mediates Hedgehog signalling
Barakat, B., Yu, L., Lo, C. Y.-W., Vu, D., Luca, E. D., Cain, J. E., Martelotto, L. G., Dedhar, S., Sadler, A. J., Wang, D., et al. (2013) · EMBO Reports · doi:10.1038/embor.2013.110 · Cited by 28 · see citing works
Cooper, M. K., Wassif, C. A., Krakowiak, P. A., Taipale, J., Gong, R., Kelley, R. I., Porter, F. D., & Beachy, P. A. (2003) · Nature Genetics · Cited by 27 · see citing works
The β2-adrenergic receptor as a surrogate odorant receptor in mouse olfactory sensory neurons
Omura, M., Grosmaître, X., Ma, M., & Mombaerts, P. (2013) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2013.10.010 · Cited by 19 · see citing works
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Cellular signalling by primary cilia in development, organ function and disease
Anvarian, Z., Mykytyn, K., Mukhopadhyay, S., Pedersen, L. B., & Christensen, S. T. (2019) · Nature Reviews Nephrology · doi:10.1038/s41581-019-0116-9 · Cited by 845 · see citing works
Self-citationPrimary Cilia and Mammalian Hedgehog Signaling
Bangs, F., & Anderson, K. V. (2017) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a028175 · Cited by 642 · see citing works
Motile and non-motile cilia in human pathology: From function to phenotypes
Mitchison, H. M., & Valente, E. M. (2017) · The Journal of Pathology · doi:10.1002/path.4843 · Cited by 448 · see citing works
Proteomics of Primary Cilia by Proximity Labeling
Mick, D. U., Rodrigues, R. B., Leib, R. D., Adams, C. M., Chien, A. S., Gygi, S. P., & Nachury, M. V. (2015) · Developmental Cell · doi:10.1016/j.devcel.2015.10.015 · Cited by 409 · see citing works
Hedgehog signaling in tissue homeostasis, cancers and targeted therapies
Jing, J., Wu, Z., Wang, J., Luo, G., Lin, H., Fan, Y., & Zhou, C. (2023) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-023-01559-5 · Cited by 261 · see citing works
Cholesterol Modification of Smoothened Is Required for Hedgehog Signaling
Xu, X., Tang, J.-J., Peng, C., Wang, Y., Fu, L., Qiu, Z.-P., Xiong, Y., Yang, L.-F., Cui, H., He, X.-L., et al. (2017) · Molecular Cell · doi:10.1016/j.molcel.2017.02.015 · Cited by 235 · see citing works
The primary cilium as a cellular receiver: organizing ciliary GPCR signaling
Hilgendorf, K. I., Johnson, C. T., & Jackson, P. K. (2016) · Current Opinion in Cell Biology · doi:10.1016/j.ceb.2016.02.008 · Cited by 224 · see citing works
Emerging mechanistic understanding of cilia function in cellular signalling
Hilgendorf, K. I., Myers, B. R., & Reiter, J. F. (2024) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-023-00698-5 · Cited by 163 · see citing works
Hedgehog receptor function during craniofacial development
Xavier, G. M., Seppala, M., Barrell, W. B., Birjandi, A. A., Geoghegan, F., & Cobourne, M. T. (2016) · Developmental Biology · doi:10.1016/j.ydbio.2016.02.009 · Cited by 144 · see citing works
Hirano, T., Katoh, Y., & Nakayama, K. (2017) · Molecular Biology of the Cell · doi:10.1091/mbc.e16-11-0813 · Cited by 141 · see citing works
Nakayama, K., & Katoh, Y. (2017) · The Journal of Biochemistry · doi:10.1093/jb/mvx087 · Cited by 130 · see citing works
MKS5 and CEP290 Dependent Assembly Pathway of the Ciliary Transition Zone
Li, C., Jensen, V. L., Park, K., Kennedy, J. E., García-Gonzalo, F. R., Romani, M., Mori, R. D., Bruel, A., Gaillard, D. A., Doray, B., et al. (2016) · PLoS Biology · doi:10.1371/journal.pbio.1002416 · Cited by 130 · see citing works
Christensen, S. T., Morthorst, S. K., Mogensen, J. B., & Pedersen, L. B. (2017) · Cold Spring Harbor Perspectives in Biology · doi:10.1101/cshperspect.a028167 · Cited by 125 · see citing works
Myers, B. R., Neahring, L., Zhang, Y., Roberts, K. J., & Beachy, P. A. (2017) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1717891115 · Cited by 125 · see citing works
Getting around the cell: physical transport in the intracellular world
Mogre, S. S., Brown, A. I., & Koslover, E. F. (2020) · Physical Biology · doi:10.1088/1478-3975/aba5e5 · Cited by 123 · see citing works
Cilia have high cAMP levels that are inhibited by Sonic Hedgehog-regulated calcium dynamics
Moore, B. S., Stepanchick, A. N., Tewson, P. H., Hartle, C. M., Zhang, J., Quinn, A. M., Hughes, T. E., & Mirshahi, T. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1602393113 · Cited by 120 · see citing works
Kast, R. E., Karpel‐Massler, G., & Halatsch, M. (2014) · Oncotarget · doi:10.18632/oncotarget.2408 · Cited by 118 · see citing works
Regulation of the oncoprotein Smoothened by small molecules
Sharpe, H. J., Wang, W., Hannoush, R. N., & de Sauvage, F. J. (2015) · Nature Chemical Biology · doi:10.1038/nchembio.1776 · Cited by 114 · see citing works
Smoothened Regulation: A Tale of Two Signals
Arensdorf, A. M., Marada, S., & Ogden, S. K. (2015) · Trends in Pharmacological Sciences · doi:10.1016/j.tips.2015.09.001 · Cited by 110 · see citing works
Endocytic Control of Cellular Signaling at the Primary Cilium
Pedersen, L. B., Mogensen, J. B., & Christensen, S. T. (2016) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2016.06.002 · Cited by 105 · see citing works
Specialized Cilia in Mammalian Sensory Systems
Falk, N., Lösl, M., Schröder, N., & Gießl, A. (2015) · Cells · doi:10.3390/cells4030500 · Cited by 110 · see citing works
The Roles of NDR Protein Kinases in Hippo Signalling
Hergovich, A. (2016) · Genes · doi:10.3390/genes7050021 · Cited by 105 · see citing works
Guo, J., Otis, J. M., Suciu, S. K., Catalano, C., Xing, L., Constable, S., Wachten, D., Gupton, S., Lee, J., Lee, A., et al. (2019) · Developmental Cell · doi:10.1016/j.devcel.2019.11.005 · Cited by 100 · see citing works
Hedgehog signaling pathway: a novel model and molecular mechanisms of signal transduction
Gorojankina, T. (2016) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-015-2127-4 · Cited by 98 · see citing works
Weßler, S., Krisch, L. M., Elmer, D. P., & Aberger, F. (2017) · Cell Communication and Signaling · doi:10.1186/s12964-017-0171-4 · Cited by 96 · see citing works
Jetten, A. M. (2018) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-018-2841-9 · Cited by 95 · see citing works
Signaling Pathways Involved in Mammalian Sex Determination and Gonad Development
Windley, S. P., & Wilhelm, D. (2015) · Sexual Development · doi:10.1159/000444065 · Cited by 95 · see citing works
Next-Generation Hedgehog/GLI Pathway Inhibitors for Cancer Therapy
Peer, E., Tesanovic, S., & Aberger, F. (2019) · Cancers · doi:10.3390/cancers11040538 · Cited by 94 · see citing works
Jiang, J., Falcone, J. L., Curci, S., & Hofer, A. M. (2019) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1819730116 · Cited by 85 · see citing works
CDKL Family Kinases Have Evolved Distinct Structural Features and Ciliary Function
Canning, P., Park, K., Gonçalves, J., Li, C., Howard, C. J., Sharpe, T., Holt, L. J., Pelletier, L., Bullock, A. N., & Leroux, M. R. (2018) · Cell Reports · doi:10.1016/j.celrep.2017.12.083 · Cited by 83 · see citing works
The intraflagellar transport machinery in ciliary signaling
Mourão, A., Christensen, S. T., & Lorentzen, E. (2016) · Current Opinion in Structural Biology · doi:10.1016/j.sbi.2016.06.009 · Cited by 83 · see citing works
Architecture of the IFT ciliary trafficking machinery and interplay between its components
Nakayama, K., & Katoh, Y. (2020) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.1080/10409238.2020.1768206 · Cited by 79 · see citing works
Emerging principles of primary cilia dynamics in controlling tissue organization and function
Gopalakrishnan, J., Feistel, K., Friedrich, B. M., Grapin‐Botton, A., Jurisch‐Yaksi, N., Mass, E., Mick, D. U., Müller, R., May‐Simera, H., Schermer, B., et al. (2023) · The EMBO Journal · doi:10.15252/embj.2023113891 · Cited by 79 · see citing works
Ramms, D. J., Raimondi, F., Arang, N., Herberg, F. W., Taylor, S. S., & Gutkind, J. S. (2021) · Pharmacological Reviews · doi:10.1124/pharmrev.120.000269 · Cited by 71 · see citing works
Schou, K. B., Mogensen, J. B., Morthorst, S. K., Nielsen, B. S., Aleliunaite, A., Serra-Marques, A., Fürstenberg, N., Saunier, S., Bizet, A. A., Veland, I. R., et al. (2017) · Nature Communications · doi:10.1038/ncomms14177 · Cited by 72 · see citing works
Ciliopathy-associated mutations of IFT122 impair ciliary protein trafficking but not ciliogenesis
Takahara, M., Katoh, Y., Nakamura, K., Hirano, T., Sugawa, M., Tsurumi, Y., & Nakayama, K. (2018) · Human Molecular Genetics · doi:10.1093/hmg/ddx421 · Cited by 62 · see citing works
Hamada, Y., Tsurumi, Y., Nozaki, S., Katoh, Y., & Nakayama, K. (2018) · Molecular Biology of the Cell · doi:10.1091/mbc.e18-03-0173 · Cited by 69 · see citing works
BBS1 is involved in retrograde trafficking of ciliary GPCRs in the context of the BBSome complex
Nozaki, S., Katoh, Y., Kobayashi, T., & Nakayama, K. (2018) · PLoS ONE · doi:10.1371/journal.pone.0195005 · Cited by 66 · see citing works
Crosstalk of Hedgehog and mTORC1 Pathways
Larsen, L. J., & Møller, L. B. (2020) · Cells · doi:10.3390/cells9102316 · Cited by 65 · see citing works
Interaction of heterotrimeric kinesin-II with IFT-B–connecting tetramer is crucial for ciliogenesis
Funabashi, T., Katoh, Y., Okazaki, M., Sugawa, M., & Nakayama, K. (2018) · Journal of Cell Biology · doi:10.1083/jcb.201801039 · Cited by 65 · see citing works
The essential role of primary cilia in cerebral cortical development and disorders
Liu, S., Trupiano, M. X., Simon, J. M., Guo, J., & Anton, E. S. (2021) · Current topics in developmental biology/Current Topics in Developmental Biology · doi:10.1016/bs.ctdb.2020.11.003 · Cited by 59 · see citing works
Hwang, S.-H., White, K. A., Somatilaka, B. N., Shelton, J. M., Richardson, J. A., & Mukhopadhyay, S. (2018) · Development · doi:10.1242/dev.154054 · Cited by 60 · see citing works
Self-citationKobayashi, T., Ishida, Y., Hirano, T., Katoh, Y., & Nakayama, K. (2020) · Molecular Biology of the Cell · doi:10.1091/mbc.e20-08-0556 · Cited by 60 · see citing works
Primary cilia are present on human blood and bone marrow cells and mediate Hedgehog signaling
Singh, M. P., Chaudhry, P., & Merchant, A. A. (2016) · Experimental Hematology · doi:10.1016/j.exphem.2016.08.009 · Cited by 53 · see citing works
Requirement of IFT-B–BBSome complex interaction in export of GPR161 from cilia
Nozaki, S., Araya, R. F. C., Katoh, Y., & Nakayama, K. (2019) · Biology Open · doi:10.1242/bio.043786 · Cited by 53 · see citing works
Shimada, I. S., Hwang, S.-H., Somatilaka, B. N., Wang, X., Skowron, P., Kim, J., Kim, M., Shelton, J. M., Rajaram, V., Xuan, Z., et al. (2018) · Cell Reports · doi:10.1016/j.celrep.2018.01.018 · Cited by 52 · see citing works
Self-citationCiliary Adenylyl Cyclases control the Hedgehog pathway
Vuolo, L., Herrera, A., Torroba, B., Menéndez, A., & Pons, S. (2015) · Journal of Cell Science · doi:10.1242/jcs.172635 · Cited by 50 · see citing works
Gruber, W., Peer, E., Elmer, D. P., Sternberg, C., Tesanovic, S., del Burgo, P. J., Coni, S., Canettieri, G., Neureiter, D., Bartz, R., et al. (2017) · International Journal of Cancer · doi:10.1002/ijc.31117 · Cited by 50 · see citing works
Regulation of ciliary membrane protein trafficking and signalling by kinesin motor proteins
Morthorst, S. K., Christensen, S. T., & Pedersen, L. B. (2018) · The FEBS Journal · doi:10.1111/febs.14583 · Cited by 49 · see citing works
Functional Divergence in the Role of N-Linked Glycosylation in Smoothened Signaling
Marada, S., Navarro, G., Truong, A., Stewart, D. P., Arensdorf, A. M., Nachtergaele, S., Angelats, E., Opferman, J. T., Rohatgi, R., McCormick, P. J., et al. (2015) · PLoS Genetics · doi:10.1371/journal.pgen.1005473 · Cited by 49 · see citing works
Self-citationNygaard, M. B., Almstrup, K., Lindbæk, L., Christensen, S. T., & Svingen, T. (2015) · Scientific Reports · doi:10.1038/srep10364 · Cited by 49 · see citing works
TSC1 and TSC2 regulate cilia length and canonical Hedgehog signaling via different mechanisms
Rosengren, T., Larsen, L. J., Pedersen, L. B., Christensen, S. T., & Møller, L. B. (2018) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-018-2761-8 · Cited by 45 · see citing works
Hedgehog signaling: From basic research to clinical applications
Yao, E., & Chuang, P. (2015) · Journal of the Formosan Medical Association · doi:10.1016/j.jfma.2015.01.005 · Cited by 48 · see citing works
Cao, M., & Zhong, Q. (2015) · Cilia · doi:10.1186/s13630-016-0027-3 · Cited by 48 · see citing works
Pilot, M., Moura, A. E., Okhlopkov, I. M., Викторович, М. Н., Manaseryan, N. H., Hayrapetyan, V., Kopaliani, N., Tsingarska, E., Alagaili, A. N., Mohammed, O. B., et al. (2021) · Evolutionary Applications · doi:10.1111/eva.13257 · Cited by 48 · see citing works
Actin filaments partition primary cilia membranes into distinct fluid corrals
Lee, S., Tan, H., Geneva, I. I., Kruglov, A., & Calvert, P. D. (2018) · The Journal of Cell Biology · doi:10.1083/jcb.201711104 · Cited by 46 · see citing works
Tsurumi, Y., Hamada, Y., Katoh, Y., & Nakayama, K. (2019) · Molecular Biology of the Cell · doi:10.1091/mbc.e18-10-0678 · Cited by 46 · see citing works
Lin, C., Yao, E., Wang, K., Nozawa, Y., Shimizu, H., Johnson, J. R., Chen, J., Krogan, N. J., & Chuang, P. (2014) · Genes & Development · doi:10.1101/gad.249425.114 · Cited by 46 · see citing works
Sonic hedgehog signaling in craniofacial development
Xu, J., Iyyanar, P. P. R., Lan, Y., & Jiang, R. (2023) · Differentiation · doi:10.1016/j.diff.2023.07.002 · Cited by 45 · see citing works
Rab35 controls cilium length, function and membrane composition
Kuhns, S., Seixas, C., Pestana, S., Tavares, B., Nogueira, R., Jacinto, R., Ramalho, J. S., Simpson, J. C., Andersen, J., Échard, A., et al. (2019) · EMBO Reports · doi:10.15252/embr.201847625 · Cited by 42 · see citing works
Robust interaction of IFT70 with IFT52–IFT88 in the IFT-B complex is required for ciliogenesis
Takei, R., Katoh, Y., & Nakayama, K. (2018) · Biology Open · doi:10.1242/bio.033241 · Cited by 44 · see citing works
Hoppe, N., Harrison, S., Hwang, S., Chen, Z.-W., Karelina, M., Deshpande, I., Suomivuori, C., Palicharla, V. R., Berry, S. P., Tschaikner, P., et al. (2024) · Nature Structural & Molecular Biology · doi:10.1038/s41594-024-01223-8 · Cited by 41 · see citing works
Self-citationNemet, I., Ropelewski, P., & Imanishi, Y. (2015) · Photochemical & Photobiological Sciences · doi:10.1039/c5pp00174a · Cited by 39 · see citing works
Somatilaka, B. N., Hwang, S., Palicharla, V. R., White, K. A., Badgandi, H., Shelton, J. M., & Mukhopadhyay, S. (2020) · Developmental Cell · doi:10.1016/j.devcel.2020.06.034 · Cited by 39 · see citing works
Self-citationNakamura, K., Noguchi, T., Takahara, M., Omori, Y., Furukawa, T., Katoh, Y., & Nakayama, K. (2020) · Journal of Biological Chemistry · doi:10.1074/jbc.ra120.014142 · Cited by 37 · see citing works
Cell signaling regulation in salivary gland development
Suzuki, A., Ogata, K., & Iwata, J. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-020-03741-2 · Cited by 37 · see citing works
Pak, E., MacKenzie, E. L., Zhao, X., Pazyra‐Murphy, M. F., Park, P. M. C., Wu, L., Shaw, D. L., Addleson, E., Cayer, S., Lopez, B. G.-C., et al. (2019) · Neuro-Oncology · doi:10.1093/neuonc/noz089 · Cited by 35 · see citing works
Absolute proteomic quantification reveals design principles of sperm flagellar chemosensation
Trötschel, C., Hamzeh, H., Alvarez, L., Pascal, R., Lavryk, F., Bönigk, W., Körschen, H. G., Müller, A., Poetsch, A., Rennhack, A., et al. (2019) · The EMBO Journal · doi:10.15252/embj.2019102723 · Cited by 35 · see citing works
Shimada, I. S., Somatilaka, B. N., Hwang, S., Anderson, A. G., Shelton, J. M., Rajaram, V., Konopka, G., & Mukhopadhyay, S. (2019) · Developmental Biology · doi:10.1016/j.ydbio.2019.03.011 · Cited by 34 · see citing works
Self-citationHoang-Minh, L., Deleyrolle, L. P., Siebzehnrubl, D., Ugartemendia, G., Futch, H. S., Griffith, B. G., Breunig, J. J., Leon, G. D., Mitchell, D. A., Semple‐Rowland, S. L., et al. (2016) · Oncotarget · doi:10.18632/oncotarget.6854 · Cited by 33 · see citing works
Qiu, H., Fujisawa, S., Nozaki, S., Katoh, Y., & Nakayama, K. (2020) · Biology Open · doi:10.1242/bio.057653 · Cited by 31 · see citing works
Primary cilia shape hallmarks of health and aging
Silva, D. F., & Cavadas, C. (2023) · Trends in Molecular Medicine · doi:10.1016/j.molmed.2023.04.001 · Cited by 31 · see citing works
Espinosa‐Bustos, C., Mella, J., Soto‐Delgado, J., & Salas, C. O. (2019) · Future Medicinal Chemistry · doi:10.4155/fmc-2018-0497 · Cited by 30 · see citing works
Primary cilia found on HeLa and other cancer cells
Kowal, T. J., & Falk, M. M. (2015) · Cell Biology International · doi:10.1002/cbin.10500 · Cited by 30 · see citing works
KIF14 controls ciliogenesis via regulation of Aurora A and is important for Hedgehog signaling
Pejšková, P., Reilly, M. L., Binó, L., Bernatík, O., Dolanská, L., Ganji, R. S., Zdráhal, Z., Benmerah, A., & Čajánek, L. (2020) · The Journal of Cell Biology · doi:10.1083/jcb.201904107 · Cited by 30 · see citing works
Okazaki, M., Kobayashi, T., Chiba, S., Takei, R., Liang, L., Nakayama, K., & Katoh, Y. (2020) · Molecular Biology of the Cell · doi:10.1091/mbc.e20-03-0208 · Cited by 29 · see citing works
Ciliary and extraciliary Gpr161 pools repress hedgehog signaling in a tissue-specific manner
Hwang, S., Somatilaka, B. N., White, K., & Mukhopadhyay, S. (2021) · eLife · doi:10.7554/elife.67121 · Cited by 28 · see citing works
Self-citationIshida, Y., Kobayashi, T., Chiba, S., Katoh, Y., & Nakayama, K. (2021) · Human Molecular Genetics · doi:10.1093/hmg/ddab034 · Cited by 27 · see citing works
Early eukaryotic origins for cilia-associated bioactive peptide-amidating activity
Kumar, D., Blaby, C., Merchant, S., Mains, R. E., King, S. M., & Eipper, B. A. (2016) · Journal of Cell Science · doi:10.1242/jcs.177410 · Cited by 26 · see citing works
Contributions of Noncanonical Smoothened Signaling During Embryonic Development
Pandit, T., & Ogden, S. K. (2017) · Journal of Developmental Biology · doi:10.3390/jdb5040011 · Cited by 26 · see citing works
TALPID3 and ANKRD26 selectively orchestrate FBF1 localization and cilia gating
Yan, H., Chen, C., Chen, H., Hong, H., Huang, Y., Ling, K., Hu, J., & Wei, Q. (2020) · Nature Communications · doi:10.1038/s41467-020-16042-w · Cited by 26 · see citing works
ARL3 and ARL13B GTPases participate in distinct steps of INPP5E targeting to the ciliary membrane
Fujisawa, S., Qiu, H., Nozaki, S., Chiba, S., Katoh, Y., & Nakayama, K. (2021) · Biology Open · doi:10.1242/bio.058843 · Cited by 25 · see citing works
Pilot, M., Malewski, T., Moura, A. E., Grzybowski, T., Oleński, K., Kamiński, S., Fadel, F. R., Alagaili, A. N., Mohammed, O. B., & Bogdanowicz, W. (2016) · G3 Genes Genomes Genetics · doi:10.1534/g3.116.029678 · Cited by 26 · see citing works
Primary Ciliary Signaling in the Skin—Contribution to Wound Healing and Scarring
Hosio, M., Jaks, V., Lagus, H., Vuola, J., Ogawa, R., & Kankuri, E. M. (2020) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2020.578384 · Cited by 22 · see citing works
Odabasi, E., Conkar, D., Deretic, J., Batman, U., Frikstad, K.-A. M., Patzke, S., & Firat‐Karalar, E. N. (2023) · Journal of Cell Science · doi:10.1242/jcs.260327 · Cited by 20 · see citing works
Naharros, I. O., Das, T., Castro, R. A., Bazán, J. F., Vaisse, C., & Nachury, M. V. (2025) · PLoS Biology · doi:10.1371/journal.pbio.3003025 · Cited by 18 · see citing works
Pituitary stalk interruption syndrome
Voutetakis, A. (2021) · Handbook of clinical neurology · doi:10.1016/b978-0-12-820683-6.00002-6 · Cited by 19 · see citing works
Sonic hedgehog enhances calcium oscillations in hippocampal astrocytes
Adachi, C., Kakinuma, N., Jo, S. H., Ishii, T., Arai, Y., Arai, S., Kitaguchi, T., Takeda, S., & Inoue, T. (2019) · Journal of Biological Chemistry · doi:10.1074/jbc.ra119.007883 · Cited by 19 · see citing works
Ciliary Signalling and Mechanotransduction in the Pathophysiology of Craniosynostosis
Tiberio, F., Parolini, O., & Lattanzi, W. (2021) · Genes · doi:10.3390/genes12071073 · Cited by 19 · see citing works
Sena, E., Feistel, K., & Durand, B. (2016) · Journal of Developmental Biology · doi:10.3390/jdb4040031 · Cited by 17 · see citing works
Hedgehog pathway, cell cycle, and primary cilium
Zhuang, T. (2025) · Cell Death Discovery · doi:10.1038/s41420-025-02605-7 · Cited by 17 · see citing works
Primary cilia function as hubs for signal transduction
Li, B., He, Y., & Yang, Z. (2025) · Cell & Bioscience · doi:10.1186/s13578-025-01471-1 · Cited by 16 · see citing works
G‐protein‐coupled receptor signaling and neural tube closure defects
Shimada, I. S., & Mukhopadhyay, S. (2016) · Birth Defects Research · doi:10.1002/bdra.23567 · Cited by 16 · see citing works
Self-citationDing, J., Shao, L., Yao, Y., Tong, X., Liu, H., Yue, S., Xie, L., & Cheng, S. Y. (2017) · Scientific Reports · doi:10.1038/s41598-017-05680-8 · Cited by 16 · see citing works
Yamazoe, T., Nagai, T., Umeda, S., Sugaya, Y., & Mizuno, K. (2020) · Journal of Biological Chemistry · doi:10.1074/jbc.ra120.013334 · Cited by 15 · see citing works
DIAPH1 regulates ciliogenesis and trafficking in primary cilia
Palander, O., & Trimble, W. S. (2020) · The FASEB Journal · doi:10.1096/fj.202001178r · Cited by 14 · see citing works
An Update of G-Protein-Coupled Receptor Signaling and Its Deregulation in Gastric Carcinogenesis
Yan, H., Zhang, J.-L., Leung, K. T., Lo, K. W., Yu, J. Q., To, K., & Kang, W. (2023) · Cancers · doi:10.3390/cancers15030736 · Cited by 13 · see citing works
Hedgehog Signaling Pathway in Fibrosis and Targeted Therapies
Hu, Y., Peng, L., Zhuo, X., Yang, C., & Zhang, Y. (2024) · Biomolecules · doi:10.3390/biom14121485 · Cited by 13 · see citing works
Patel, K., & Smith, N. J. (2023) · British Journal of Pharmacology · doi:10.1111/bph.16053 · Cited by 13 · see citing works
- Authors
- Mukhopadhyay, S., & Rohatgi, R.
- Affiliations
- The University of Texas Southwestern Medical Center (US)
- Stanford Medicine (US)
- Corresponding author
- Mukhopadhyay, Saikat
- Rohatgi, Rajat
- Venue
- Seminars in Cell & Developmental Biology
- Publisher
- Elsevier BV
- Published
- 2014-09
- Volume
- 33
- Pages
- 63-72
- ISSN
- 1084-9521 (ISSN-L)
- PMC
- PMC4130902
- OpenAlex
- W1986320552
- Cited by
- 142
- References
- 145
- Citations by year
- 2026: 4 · 2025: 10 · 2024: 7 · 2023: 9 · 2022: 3 · 2021: 13 · 2020: 15 · 2019: 14 · 2018: 17 · 2017: 14 · 2016: 19 · 2015: 15 · 2014: 2
- FWCI
- 1.57
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Seminars in Cell and Developmental Biology (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- NIH Common Fund
- Pew Foundation
- Sontag Foundation
- March of Dimes Foundation
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Hedgehog Signaling Pathway Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic and Kidney Cyst Diseases
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Receptor Mechanisms and Signaling
- Keywords
- Hedgehog signaling, primary cilia, G protein-coupled receptors, Smoothened, GPR161, cancer therapy
- MeSH terms
- Animals, Cilia, Humans, Signal Transduction, Body Patterning, Receptors, G-Protein-Coupled, Hedgehog Proteins
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