The DOI matches its Crossref record; 34 of the 34 references it cites were found in a registry or an index.
Control of β-Catenin Stability
Open accessAbstract
Regulation of beta-catenin degradation by intracellular components of the wnt pathway was reconstituted in cytoplasmic extracts of Xenopus eggs and embryos. The ubiquitin-dependent beta-catenin degradation in extracts displays a biochemical requirement for axin, GSK3, and APC. Axin dramatically accelerates while dishevelled inhibits beta-catenin turnover. Through another domain, dishevelled recruits GBP/Frat1 to the APC-axin-GSK3 complex. Our results confirm and extend models in which inhibition of GSK3 has two synergistic effects: (1) reduction of APC phosphorylation and loss of affinity for beta-catenin and (2) reduction of beta-catenin phosphorylation and consequent loss of its affinity for the SCF ubiquitin ligase complex. Dishevelled thus stabilizes beta-catenin, which can dissociate from the APC/axin complex and participate in transcriptional activation.
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“In the case of the activity CSM1 from Lee et al. (2003), several wet-lab data from their own experiments (WD1–WD5) as well as from Salic et al. (2000) [66] (WD1–WD3) are used during the calibration of the model SM1 which produces a Simulation Experiment SE1, the corresponding Simulation Data SD1 as well as the calibrated Simulation Model SM2.”
From Relating simulation studies by provenance—Developing a family of Wnt signaling models (2021) · cites this paper as [66]
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Cites
β‐catenin is a target for the ubiquitin–proteasome pathway
Aberle, H., Bauer, A., Stappert, J., Kispert, A., & Kemler, R. (1997) · The EMBO Journal · doi:10.1093/emboj/16.13.3797 · Cited by 2,586
Wnt signaling: a common theme in animal development
Cadigan, K. M., & Nusse, R. (1997) · Genes & Development · doi:10.1101/gad.11.24.3286 · Cited by 2,567
A molecular mechanism for the effect of lithium on development.
Klein, P. S., & Melton, D. A. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.16.8455 · Cited by 2,334
MECHANISMS OF WNT SIGNALING IN DEVELOPMENT
Wodarz, A., & Nusse, R. (1998) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.14.1.59 · Cited by 2,030
XTcf-3 Transcription Factor Mediates β-Catenin-Induced Axis Formation in Xenopus Embryos
Molenaar, M., van de Wetering, M., Oosterwegel, M., Peterson-Maduro, J., Godsave, S., Korinek, V., Roose, J., Destrée, O., & Clevers, H. (1996) · Cell · doi:10.1016/s0092-8674(00)80112-9 · Cited by 1,824
A new member of the frizzled family from Drosophila functions as a Wingless receptor
Bhanot, P., van den Brink, M. R. M., Samos, C. H., Hsieh, J.-C., Wang, Y., Macke, J. P., Andrew, D. J., Nathans, J., & Nusse, R. (1996) · Nature · doi:10.1038/382225a0 · Cited by 1,504
Binding of GSK3β to the APC-β-Catenin Complex and Regulation of Complex Assembly
Rubinfeld, B., Albert, I., Porfiri, E., Fiol, C. J., Munemitsu, S. M., & Polakis, P. G. (1996) · Science · doi:10.1126/science.272.5264.1023 · Cited by 1,420
Functional Interaction of an Axin Homolog, Conductin, with β-Catenin, APC, and GSK3β
Behrens, J., Jerchow, B., Würtele, M., Grimm, J., Asbrand, C., Wirtz, R. M., Kühl, M., Wedlich, D., & Birchmeier, W. (1998) · Science · doi:10.1126/science.280.5363.596 · Cited by 1,255
Yost, C., Torres, M., Miller, J., Huang, E., Kimelman, D., & Moon, R. T. (1996) · Genes & Development · doi:10.1101/gad.10.12.1443 · Cited by 1,167
King, R. W., Peters, J., Tugendreich, S., Rolfe, M., Hieter, P., & Kirschner, M. W. (1995) · Cell · doi:10.1016/0092-8674(95)90338-0 · Cited by 956
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Ghoneim, M. A., Adhmallah, A. K., Awaad, H., El‐Din, A. B. S., Kock, N. G., & Whitmore, W. F. (1988) · PubMed · Cited by 2
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McDowell, G. S., & Philpott, A. (2018) · Cold Spring Harbor Protocols · doi:10.1101/pdb.prot104513 · Cited by 1
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Dzeyk, J. (2012) · Otago University Research Archive (University of Otago)
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Conrad, W. H. (2012) · ResearchWorks at the University of Washington (University of Washington)
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Das, U. N. (2010) · Wiley eBooks · doi:10.1002/9780813820637.ch18
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Zou, Y., Goetz, E. M., Suzuki, M., & Boothman, D. A. (2009) · Springer eBooks · doi:10.1007/978-4-431-88659-4_26
Kinase Regulation of XIAP in Wnt Signaling
Hang, B. I. (2016)
The role of CD44 in Wnt/β-catenin signaling
Schmitt, M. (2014) · Repository KITopen (Karlsruhe Institute of Technology) · doi:10.5445/ir/1000043638
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Jones, W. M., & Bejsovec, A. (2003)
Cherian, J. R., & Petrella, L. N. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/811414
Cherian, J. R. (2020) · e-Publications@Marquette (Marquette University)
LiuChengliang, G. G., Zhang, Z., & MaoPeng, X. (2009)
Investigations into the Interaction between Src Kinase and Wnt Signaling
Tang, P. L. (2009) · Libraries and Cultural Resources (University of Calgary) · doi:10.11575/prism/14854
The effect of Wnt isoforms on myogenesis.
McColl, R. S. (2014) · ResearchSpace (University of KwaZulu-Natal)
Monga, S. P., & Michalopoulos, G. K. (2005) · Springer eBooks · doi:10.1007/3-540-27194-5_15
Monga, S. P. (2015) · Wiley eBooks · doi:10.1002/9781118663387.ch18
Chemical Genetics Reveals a Role of Squalene Synthase in TGFβ Signaling and Cardiomyogenesis
Takemoto, Y., Kadota, S., Minami, I., Otsuka, S., Okuda, S., Abo, M., Punzalan, L. L., Shen, Y., Shiba, Y., & Uesugi, M. (2021) · Angewandte Chemie · doi:10.1002/ange.202100523
Adult Diseases and Low-Grade Systemic Inflammation Have Their Origins in the Perinatal Period
Das, U. N. (2011) · Springer eBooks · doi:10.1007/978-94-007-0495-4_16
Signaling pathway and pharmacology
Li, X. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-15793-6.00005-6
Choi, J., Lee, H.-S., Kim, H. J., Choi, M., Tallei, T. E., Ahn, C., So, J.-H., Park, M. N., & Kim, B. (2026) · Fitoterapia · doi:10.1016/j.fitote.2026.107115
Role of VDAC1 hypoxic form, VDAC1-∆C, in the expression of primary cilia and tumor progression
Fabbri, L. (2019) · theses.fr (ABES) · doi:10.70675/7a53239dzc652z4ea4z8b95z4a71961c83b4
Karnam, A. (2019) · theses.fr (ABES) · doi:10.70675/ae464b4az3b90z42fazb943ze3b07d12e80f
BindingDB (2014) · UC San Diego · doi:10.7270/q2474c9c
BindingDB (2023) · UC San Diego · doi:10.7270/q27h1pk7
Metadata
- Authors
- Salic, A., Lee, E., Mayer, L., & Kirschner, M. W.
- Affiliations
- Harvard University (US)
- Corresponding author
- Kirschner, Marc W.
- Venue
- Molecular Cell
- Publisher
- Elsevier BV
- Published
- 2000-03
- Volume
- 5
- Issue
- 3
- Pages
- 523-532
- ISSN
- 1097-2765 (ISSN-L)
- OpenAlex
- W2069704514
- Cited by
- 335
- References
- 34
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 1 · 2023: 4 · 2022: 4 · 2021: 10 · 2020: 11 · 2019: 12 · 2018: 11 · 2017: 11 · 2016: 16 · 2015: 5 · 2014: 16 · 2013: 16 · 2012: 16
- FWCI
- 8.68
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Molecular Cell (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Wnt/β-catenin signaling in development and cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Signaling Pathways in Disease
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ubiquitin and proteasome pathways
- Keywords
- β-catenin stability, Wnt signaling, ubiquitin-mediated proteolysis, Axin, glycogen synthase kinase-3, APC, Dishevelled, SCF ubiquitin ligase, protein phosphorylation, Xenopus egg extracts, transcriptional activation
- MeSH terms
- Dishevelled Proteins, Animals, Carrier Proteins, Cell-Free System, Cytoplasm, Cytoskeletal Proteins, Models, Biological, Ovum, Phosphoproteins, Phosphorylation, Protein Binding, Proteins, Proto-Oncogene Proteins, Repressor Proteins, Subcellular Fractions, Ubiquitins, Xenopus, Trans-Activators, Protein Structure, Tertiary, Calcium-Calmodulin-Dependent Protein Kinases, Adenomatous Polyposis Coli Protein, Xenopus Proteins, Zebrafish Proteins, Glycogen Synthase Kinase 3, Intracellular Signaling Peptides and Proteins, Adaptor Proteins, Signal Transducing, Wnt Proteins, beta Catenin, Axin Protein
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