Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.
Sci. Signal., 2 September 2008
Vol. 1, Issue 35, p. re9
[DOI: 10.1126/scisignal.135re9]
REVIEWS
Alternative Wnt Signaling Is Initiated by Distinct Receptors
Renée van Amerongen*,
Amanda Mikels*, and
Roel Nusse
Howard Hughes Medical Institute, Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.
* These authors contributed equally to this work.
Abstract:
An unanswered question in the field of signal transduction research is how different signaling pathways are activated with strict specificity in a temporally and spatially controlled manner. Because extracellular ligands and membrane receptors constitute the first signaling modalities for most pathways, selectivity in ligand-receptor binding likely dictates the outcome of downstream signaling events. Unfortunately, possible complexities underlying ligand-receptor interactions are often overlooked. Here, we discuss basic principles of signal transduction initiated at the cell membrane, with the Wnt pathway, which harbors a multitude of ligands and receptors, as an example.
The editors suggest the following Related Resources on Science sites:
In Science Signaling
EDITORS' CHOICE
L. Bryan Ray (11 December 2012) Sci. Signal.5 (254), ec319.
[DOI: 10.1126/scisignal.2003850] |Abstract »
MEETING REPORTS
Folkert Verkaar, Ken M. Cadigan, and Renée van Amerongen (11 December 2012) Sci. Signal.5 (254), mr2.
[DOI: 10.1126/scisignal.2003714] |Abstract »|Full Text »|PDF »
PODCASTS
K. Christopher Garcia and Annalisa M. VanHook (3 July 2012) Sci. Signal.5 (231), pc15.
[DOI: 10.1126/scisignal.2003307] |Abstract »|Full Text »|Podcast »
EDITORS' CHOICE
Nancy R. Gough (12 June 2012) Sci. Signal.5 (228), ec162.
[DOI: 10.1126/scisignal.2003300] |Abstract »
PRESENTATIONS
B. Ian Hutchins, Li Li, and Katherine Kalil (10 January 2012) Sci. Signal.5 (206), pt1.
[DOI: 10.1126/scisignal.2002523] |Abstract »|Full Text »|PDF »|Slideshow »
EDITORIAL GUIDES
Nancy R. Gough (10 January 2012) Sci. Signal.5 (206), eg2.
[DOI: 10.1126/scisignal.2002806] |Abstract »|Full Text »|PDF »
EDITORS' CHOICE
Nancy R. Gough (10 May 2011) Sci. Signal.4 (172), ec134.
[DOI: 10.1126/scisignal.4172ec134] |Abstract »
RESEARCH ARTICLES
Leni S. Jacob, Xiaofeng Wu, Michael E. Dodge, Chih-Wei Fan, Ozlem Kulak, Baozhi Chen, Wei Tang, Baolin Wang, James F. Amatruda, and Lawrence Lum (25 January 2011) Sci. Signal.4 (157), ra4.
[DOI: 10.1126/scisignal.2001225] |Editor's Summary »|Abstract »|Full Text »|PDF »|Supplementary Materials »
EDITORS' CHOICE
Annalisa M. VanHook (23 November 2010) Sci. Signal.3 (149), ec356.
[DOI: 10.1126/scisignal.3149ec356] |Abstract »
PRESENTATIONS
Li Li, B. Ian Hutchins, and Katherine Kalil (9 November 2010) Sci. Signal.3 (147), pt2.
[DOI: 10.1126/scisignal.3147pt2] |Abstract »|Full Text »|PDF »|Slideshow »
EDITORS' CHOICE
Paula A. Kiberstis (27 July 2010) Sci. Signal.3 (132), ec229.
[DOI: 10.1126/scisignal.3132ec229] |Abstract »
RESEARCH ARTICLES
Kristin K. Jernigan, Christopher S. Cselenyi, Curtis A. Thorne, Alison J. Hanson, Emilios Tahinci, Nicole Hajicek, William M. Oldham, Laura A. Lee, Heidi E. Hamm, John R. Hepler, Tohru Kozasa, Maurine E. Linder, and Ethan Lee (11 May 2010) Sci. Signal.3 (121), ra37.
[DOI: 10.1126/scisignal.2000647] |Editor's Summary »|Abstract »|Full Text »|PDF »|Supplementary Materials »
EDITORS' CHOICE
Wei Wong (5 January 2010) Sci. Signal.3 (103), ec2.
[DOI: 10.1126/scisignal.3103ec2] |Abstract »
EDITORS' CHOICE
Wei Wong (17 March 2009) Sci. Signal.2 (62), ec96.
[DOI: 10.1126/scisignal.262ec96] |Abstract »
EDITORS' CHOICE
Wei Wong (25 November 2008) Sci. Signal.1 (47), ec401.
[DOI: 10.1126/scisignal.147ec401] |Abstract »
EDITORS' CHOICE
John F. Foley (18 November 2008) Sci. Signal.1 (46), ec393.
[DOI: 10.1126/scisignal.146ec393] |Abstract »
PODCASTS
Michael B. Major, Randall T. Moon, and Annalisa M. VanHook (11 November 2008) Sci. Signal.1 (45), pc11.
[DOI: 10.1126/scisignal.145pc11] |Abstract »|Full Text »|Podcast »
PERSPECTIVES
Nate P. Hoverter and Marian L. Waterman (30 September 2008) Sci. Signal.1 (39), pe43.
[DOI: 10.1126/scisignal.139pe43] |Abstract »|Full Text »|PDF »
PERSPECTIVES
Christopher S. Cselenyi and Ethan Lee (26 February 2008) Sci. Signal.1 (8), pe10.
[DOI: 10.1126/stke.18pe10] |Abstract »|Full Text »|PDF »
PERSPECTIVES
Benjamin N. R. Cheyette (14 December 2004) Sci. STKE2004 (263), pe54.
[DOI: 10.1126/stke.2632004pe54] |Abstract »|Full Text »|PDF »
TEACHING RESOURCES
Randall T. Moon (6 July 2004) Sci. STKE2004 (240), tr5.
[DOI: 10.1126/stke.2402004tr5] |Abstract »|Resource Details »
THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Ptk7 promotes non-canonical Wnt/PCP-mediated morphogenesis and inhibits Wnt/{beta}-catenin-dependent cell fate decisions during vertebrate development.
M. Hayes, M. Naito, A. Daulat, S. Angers, and B. Ciruna (2013)
Development
140, 1807-1818
|Abstract »|Full Text »|PDF »
Frizzled and LRP5/6 Receptors for Wnt/{beta}-Catenin Signaling.
B. T. MacDonald and X. He (2012)
Cold Spring Harb Perspect Biol
4, a007880
|Abstract »|Full Text »|PDF »
Transcriptome-level microarray expression profiling implicates IGF-1 and Wnt signalling dysregulation in the pathogenesis of thyroid-associated orbitopathy.
D. G. Ezra, J. Krell, G. E. Rose, M. Bailly, J. Stebbing, and L. Castellano (2012)
J. Clin. Pathol.
65, 608-613
|Abstract »|Full Text »|PDF »
R. Nusse (2012)
Cold Spring Harb Perspect Biol
4, a011163
|Full Text »|PDF »
Wnt/{beta}-catenin signaling requires interaction of the Dishevelled DEP domain and C terminus with a discontinuous motif in Frizzled.
D. V. F. Tauriello, I. Jordens, K. Kirchner, J. W. Slootstra, T. Kruitwagen, B. A. M. Bouwman, M. Noutsou, S. G. D. Rudiger, K. Schwamborn, A. Schambony, et al. (2012)
PNAS
109, E812-E820
|Abstract »|Full Text »|PDF »
Wnt5a-Ror-Dishevelled signaling constitutes a core developmental pathway that controls tissue morphogenesis.
H.-Y. H. Ho, M. W. Susman, J. B. Bikoff, Y. K. Ryu, A. M. Jonas, L. Hu, R. Kuruvilla, and M. E. Greenberg (2012)
PNAS
109, 4044-4051
|Abstract »|Full Text »|PDF »
Wilms Tumor Gene on X Chromosome (WTX) Inhibits Degradation of NRF2 Protein through Competitive Binding to KEAP1 Protein.
N. D. Camp, R. G. James, D. W. Dawson, F. Yan, J. M. Davison, S. A. Houck, X. Tang, N. Zheng, M. B. Major, and R. T. Moon (2012)
J. Biol. Chem.
287, 6539-6550
|Abstract »|Full Text »|PDF »
Neural crest specification by noncanonical Wnt signaling and PAR-1.
Probing transcription-specific outputs of {beta}-catenin in vivo.
T. Valenta, M. Gay, S. Steiner, K. Draganova, M. Zemke, R. Hoffmans, P. Cinelli, M. Aguet, L. Sommer, and K. Basler (2011)
Genes & Dev.
25, 2631-2643
|Abstract »|Full Text »|PDF »
Wnt5a is a cell-extrinsic factor that supports self-renewal of mouse spermatogonial stem cells.
Canonical and noncanonical Wnts use a common mechanism to activate completely unrelated coreceptors.
L. Grumolato, G. Liu, P. Mong, R. Mudbhary, R. Biswas, R. Arroyave, S. Vijayakumar, A. N. Economides, and S. A. Aaronson (2010)
Genes & Dev.
24, 2517-2530
|Abstract »|Full Text »|PDF »
The Role of Wnt Signaling in Physiological and Pathological Angiogenesis.
The Embryonic Transcription Cofactor LBH Is a Direct Target of the Wnt Signaling Pathway in Epithelial Development and in Aggressive Basal Subtype Breast Cancers.
M. E. Rieger, A. H. Sims, E. R. Coats, R. B. Clarke, and K. J. Briegel (2010)
Mol. Cell. Biol.
30, 4267-4279
|Abstract »|Full Text »|PDF »
Trafficking, Acidification, and Growth Factor Signaling.
Development of small molecules targeting the Wnt pathway for the treatment of colon cancer: a high-throughput screening approach.
W. Chen, M. Chen, and L. S. Barak (2010)
Am J Physiol Gastrointest Liver Physiol
299, G293-G300
|Abstract »|Full Text »|PDF »
Wnt5b-Ryk pathway provides directional signals to regulate gastrulation movement.
S. Lin, L. M. Baye, T. A. Westfall, and D. C. Slusarski (2010)
J. Cell Biol.
190, 263-278
|Abstract »|Full Text »|PDF »
Control of hair follicle cell fate by underlying mesenchyme through a CSL-Wnt5a-FoxN1 regulatory axis.
B. Hu, K. Lefort, W. Qiu, B.-C. Nguyen, R. D. Rajaram, E. Castillo, F. He, Y. Chen, P. Angel, C. Brisken, et al. (2010)
Genes & Dev.
24, 1519-1532
|Abstract »|Full Text »|PDF »
Frizzled-5, a receptor for the synaptic organizer Wnt7a, regulates activity-mediated synaptogenesis.
The Inorganic Pyrophosphate Transporter ANK Preserves the Differentiated Phenotype of Articular Chondrocyte.
F. Cailotto, S. Sebillaud, P. Netter, J.-Y. Jouzeau, and A. Bianchi (2010)
J. Biol. Chem.
285, 10572-10582
|Abstract »|Full Text »|PDF »
Osteocytes and WNT: the Mechanical Control of Bone Formation.
C. Galli, G. Passeri, and G. M. Macaluso (2010)
Journal of Dental Research
89, 331-343
|Abstract »|PDF »
Reconstitution of a Frizzled8{middle dot}Wnt3a{middle dot}LRP6 Signaling Complex Reveals Multiple Wnt and Dkk1 Binding Sites on LRP6.
E. Bourhis, C. Tam, Y. Franke, J. F. Bazan, J. Ernst, J. Hwang, M. Costa, A. G. Cochran, and R. N. Hannoush (2010)
J. Biol. Chem.
285, 9172-9179
|Abstract »|Full Text »|PDF »
G Protein-coupled Receptor Kinases Phosphorylate LRP6 in the Wnt Pathway.
M. Chen, M. Philipp, J. Wang, R. T. Premont, T. R. Garrison, M. G. Caron, R. J. Lefkowitz, and W. Chen (2009)
J. Biol. Chem.
284, 35040-35048
|Abstract »|Full Text »|PDF »
Wnt-Ror signaling to SIA and SIB neurons directs anterior axon guidance and nerve ring placement in C. elegans.
J. R. Kennerdell, R. D. Fetter, and C. I. Bargmann (2009)
Development
136, 3801-3810
|Abstract »|Full Text »|PDF »
Ror2 Receptor Requires Tyrosine Kinase Activity to Mediate Wnt5A Signaling.