The DOI matches its Crossref record; 30 of the 30 references it cites were found in a registry or an index.
Wnt proteins are lipid-modified and can act as stem cell growth factors
Abstract
Wnt signalling is involved in numerous events in animal development, including the proliferation of stem cells and the specification of the neural crest. Wnt proteins are potentially important reagents in expanding specific cell types, but in contrast to other developmental signalling molecules such as hedgehog proteins and the bone morphogenetic proteins, Wnt proteins have never been isolated in an active form. Although Wnt proteins are secreted from cells, secretion is usually inefficient and previous attempts to characterize Wnt proteins have been hampered by their high degree of insolubility. Here we have isolated active Wnt molecules, including the product of the mouse Wnt3a gene. By mass spectrometry, we found the proteins to be palmitoylated on a conserved cysteine. Enzymatic removal of the palmitate or site-directed and natural mutations of the modified cysteine result in loss of activity, and indicate that the lipid is important for signalling. The purified Wnt3a protein induces self-renewal of haematopoietic stem cells, signifying its potential use in tissue engineering.
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“Studies have revealed that the Wnt proteins are glycosylated in the endoplasmic reticulum and also are palmitolated.9,10”
From Wnt signal transduction pathways (2008) · cites this paper as [10]
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Cites
Large-scale analysis of the yeast proteome by multidimensional protein identification technology
Washburn, M. P., Wolters, D. A., & Yates, J. R. (2001) · Nature Biotechnology · doi:10.1038/85686 · Cited by 4,768
Self-citationPhase separation of integral membrane proteins in Triton X-114 solution.
Bordier, C. (1981) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)69848-0 · Cited by 3,324
Polakis, P. (2000) · Genes & Development · doi:10.1101/gad.14.15.1837 · Cited by 3,183
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
Self-citationA role for Wnt signalling in self-renewal of haematopoietic stem cells
Reya, T., Duncan, A. W., Ailles, L., Domen, J., Scherer, D. C., Willert, K., Hintz, L., Nusse, R., & Weissman, I. L. (2003) · Nature · doi:10.1038/nature01593 · Cited by 2,159
Self-citationThe β-Catenin/TCF-4 Complex Imposes a Crypt Progenitor Phenotype on Colorectal Cancer Cells
van de Wetering, M., Sancho, E., Verweij, C., de Lau, W., Oving, I., Hurlstone, A., van der Horn, K., Batlle, E., Coudreuse, D., Haramis, A.-P., et al. (2002) · Cell · doi:10.1016/s0092-8674(02)01014-0 · Cited by 2,030
Tabb, D. L., McDonald, W. H., & Yates, J. R. (2002) · Journal of Proteome Research · doi:10.1021/pr015504q · Cited by 1,369
Self-citationIdentification of a Palmitic Acid-modified Form of Human Sonic hedgehog
Pepinsky, R. B., Zeng, C., Wen, D., Rayhorn, P., Baker, D. P., Williams, K. P., Bixler, S. A., Ambrose, C. M., Garber, E. A., Miatkowski, K., et al. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.22.14037 · Cited by 754
Wnt Signaling and an APC-Related Gene Specify Endoderm in Early C. elegans Embryos
Rocheleau, C. E., Downs, W. D., Lin, R., Wittmann, C., Bei, Y., Cha, Y.-H., Ali, M., Priess, J. R., & Mello, C. C. (1997) · Cell · doi:10.1016/s0092-8674(00)80531-0 · Cited by 660
Shotgun identification of protein modifications from protein complexes and lens tissue
MacCoss, M. J., McDonald, W. H., Saraf, A., Sadygov, R. G., Clark, J., Tasto, J. J., Gould, K. L., Wolters, D. A., Washburn, M. P., Weiss, A., et al. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.122231399 · Cited by 593
Self-citationEctodermal Wnt Function as a Neural Crest Inducer
García‐Castro, M. I., Marcelle, C., & Bronner-Fraser, M. E. (2002) · Science · doi:10.1126/science.1070824 · Cited by 537
A superfamily of membrane-bound O -acyltransferases with implications for Wnt signaling
Hofmann, K. (2000) · Trends in Biochemical Sciences · doi:10.1016/s0968-0004(99)01539-x · Cited by 495
A Cytoplasmic Acyl-Protein Thioesterase That Removes Palmitate from G Protein α Subunits and p21RAS
Duncan, J. A., & Gilman, A. G. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.25.15830 · Cited by 405
dishevelled and armadillo act in the Wingless signalling pathway in Drosophila
Noordermeer, J. N., Klingensmith, J., Perrimon, N., & Nusse, R. (1994) · Nature · doi:10.1038/367080a0 · Cited by 378
Self-citationHsieh, J.-C., Rattner, A., Smallwood, P. M., & Nathans, J. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.7.3546 · Cited by 349
Kadowaki, T., Wilder, E. L., Klingensmith, J., Zachary, K., & Perrimon, N. (1996) · Genes & Development · doi:10.1101/gad.10.24.3116 · Cited by 348
Roelink, H., & Nusse, R. (1991) · Genes & Development · doi:10.1101/gad.5.3.381 · Cited by 285
Self-citationCytoskeletal reorganization by soluble Wnt‐3a protein signalling
Shibamoto, Higano, K., Takada, R., Ito, F., Takeichi, M., & Takada, S. (1998) · Genes to Cells · doi:10.1046/j.1365-2443.1998.00221.x · Cited by 251
A Wnt signaling pathway controls Hox gene expression and neuroblast migration in C. elegans
Maloof, J., Whangbo, J., Harris, J. M., Jongeward, G. D., & Kenyon, C. J. (1999) · Development · doi:10.1242/dev.126.1.37 · Cited by 245
LEF-1/TCF Proteins Mediate Wnt-Inducible Transcription from the Xenopus Nodal-Related 3 Promoter
McKendry, R., Hsu, S.-C., Harland, R. M., & Grosschedl, R. (1997) · Developmental Biology · doi:10.1006/dbio.1997.8797 · Cited by 242
Domen, J., & Weissman, I. L. (2000) · The Journal of Experimental Medicine · doi:10.1084/jem.192.12.1707 · Cited by 219
Self-citationSecreted int-1 Protein Is Associated with the Cell Surface
Papkoff, J. S., & Schryver, B. B. (1990) · Molecular and Cellular Biology · doi:10.1128/mcb.10.6.2723 · Cited by 210
Biological activity of soluble wingless protein in cultured Drosophila imaginal disc cells
van Leeuwen, F. N., Samos, C. H., & Nusse, R. (1994) · Nature · doi:10.1038/368342a0 · Cited by 192
Self-citationLigand Receptor Interactions in the Wnt Signaling Pathway inDrosophila
Wu, C.-H., & Nusse, R. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m207850200 · Cited by 190
Self-citationTanaka, K., Kitagawa, Y., & Kadowaki, T. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m200187200 · Cited by 184
Notch is required for wingless signaling in the epidermis of Drosophila
Couso, J. P. (1994) · Cell · doi:10.1016/0092-8674(94)90195-3 · Cited by 179
Activation ofSiamoisby theWntPathway
Brannon, M. K., & Kimelman, D. (1996) · Developmental Biology · doi:10.1006/dbio.1996.0306 · Cited by 134
Mason, J. O., Kitajewski, J., & VARMUS, H. E. (1992) · Molecular Biology of the Cell · doi:10.1091/mbc.3.5.521 · Cited by 111
Biochemical Analysis of Murine Wnt Proteins Reveals both Shared and Distinct Properties
Burrus, L. W., & McMahon, A. P. (1995) · Experimental Cell Research · doi:10.1006/excr.1995.1327 · Cited by 94
A Soluble Form of Wnt-1 Protein with Mitogenic Activity on Mammary Epithelial Cells
Bradley, R. S., & Brown, A. M. C. (1995) · Molecular and Cellular Biology · doi:10.1128/mcb.15.8.4616 · Cited by 80
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MacDonald, B. T., Tamai, K., & He, X. (2009) · Developmental Cell · doi:10.1016/j.devcel.2009.06.016 · Cited by 5,583
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Logan, C. Y., & Nusse, R. (2004) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.20.010403.113126 · Cited by 5,325
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Self-citation
Metadata
- Authors
- Willert, K., Brown, J. D., Danenberg, E., Duncan, A. W., Weissman, I. L., Reya, T., Yates, J. R., & Nusse, R.
- Affiliations
- Howard Hughes Medical Institute (US)
- Duke University (US)
- Stanford Medicine (US)
- Scripps Research Institute (US)
- ORCID
- Venue
- Nature
- Published
- 2003-04-27
- Volume
- 423
- Issue
- 6938
- Pages
- 448-452
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- OpenAlex
- W2147864074
- Cited by
- 2,257
- References
- 30
- Citations by year
- 2026: 40 · 2025: 42 · 2024: 48 · 2023: 54 · 2022: 63 · 2021: 63 · 2020: 78 · 2019: 87 · 2018: 86 · 2017: 90 · 2016: 100 · 2015: 101 · 2014: 99 · 2013: 106 · 2012: 133
- FWCI
- 48.13
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Funders
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK067834)
- 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 › Hedgehog Signaling Pathway Studies
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Keywords
- Wnt proteins, Wnt3a, palmitoylation, lipid modification, cysteine modification, Wnt signaling, hematopoietic stem cells, stem cell self-renewal, stem cell growth factor, tissue engineering, neural crest specification, protein purification
- MeSH terms
- Amino Acid Sequence, Animals, Cell Differentiation, Cell Division, Cysteine, Cytoskeletal Proteins, Drosophila melanogaster, Growth Substances, Hematopoietic Stem Cells, L Cells, Molecular Sequence Data, Palmitic Acids, Proteins, Solubility, Xenopus laevis, Signal Transduction, Trans-Activators, Mutagenesis, Site-Directed, Conserved Sequence, Hematopoietic Stem Cell Transplantation, Xenopus Proteins, Zebrafish Proteins, Lipid Metabolism, Wnt Proteins, beta Catenin, Mice, Wnt3 Protein, Wnt3A Protein
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