Wise, a context-dependent activator and inhibitor of Wnt signalling

We have isolated a novel secreted molecule, Wise, by a functional screen for activities that alter the anteroposterior character of neuralised Xenopus animal caps. Wise encodes a secreted protein capable of inducing posterior neural markers at a distance. Phenotypes arising from ectopic expression or depletion of Wise resemble those obtained when Wnt signalling is altered. In animal cap assays, posterior neural markers can be induced by Wnt family members, and induction of these markers by Wise requires components of the canonical Wnt pathway. This indicates that in this context Wise activates the Wnt signalling cascade by mimicking some of the effects of Wnt ligands. Activation of the pathway was further confirmed by nuclear accumulation of β-catenin driven by Wise. By contrast, in an assay for secondary axis induction, extracellularly Wise antagonises the axis-inducing ability of Wnt8. Thus, Wise can activate or inhibit Wnt signalling in a context-dependent manner. The Wise protein physically interacts with the Wnt co-receptor, lipoprotein receptor-related protein 6 (LRP6), and is able to compete with Wnt8 for binding to LRP6. These activities of Wise provide a new mechanism for integrating inputs through the Wnt coreceptor complex to modulate the balance of Wnt signalling.

[1]  Viktor Hamburger,et al.  A series of normal stages in the development of the chick embryo , 1992, Journal of morphology.

[2]  J. Smith,et al.  Xenopus Cyr61 regulates gastrulation movements and modulates Wnt signalling , 2003, Development.

[3]  R. Wallace,et al.  Protein incorporation by isolated amphibian oocytes. V. Specificity for vitellogenin incorporation , 1976, The Journal of cell biology.

[4]  M. Bonnin,et al.  Hox gene induction in the neural tube depends on three parameters: competence, signal supply and paralogue group. , 1997, Development.

[5]  R. Moon,et al.  Direct regulation of the Xenopus engrailed-2 promoter by the Wnt signaling pathway, and a molecular screen for Wnt-responsive genes, confirm a role for Wnt signaling during neural patterning in Xenopus , 1999, Mechanisms of Development.

[6]  R. Krumlauf,et al.  The Wnt/beta-catenin pathway posteriorizes neural tissue in Xenopus by an indirect mechanism requiring FGF signalling. , 2001, Developmental biology.

[7]  J. Smith,et al.  Bix1, a direct target of Xenopus T-box genes, causes formation of ventral mesoderm and endoderm. , 1998, Development.

[8]  H. Sive,et al.  Xenopus hindbrain patterning requires retinoid signaling. , 1997, Developmental biology.

[9]  C. Tabin,et al.  Control of Dorsoventral Somite Patterning by Wnt-1 and β-Catenin , 1998 .

[10]  S. Fraser,et al.  Specification of the zebrafish nervous system by nonaxial signals. , 1997, Science.

[11]  A. Joyner,et al.  The midbrain-hindbrain phenotype of Wnt-1− Wnt-1− mice results from stepwise deletion of engrailed-expressing cells by 9.5 days postcoitum , 1992, Cell.

[12]  C. Niehrs,et al.  Kremen proteins interact with Dickkopf1 to regulate anteroposterior CNS patterning , 2002, Development.

[13]  S. Sokol,et al.  Graded amounts of Xenopus dishevelled specify discrete anteroposterior cell fates in prospective ectoderm , 1997, Mechanisms of Development.

[14]  R. Kemler,et al.  The C-terminal transactivation domain of β-catenin is necessary and sufficient for signaling by the LEF-1/β-catenin complex in Xenopus laevis , 1999, Mechanisms of Development.

[15]  References , 1971 .

[16]  T. Jessell,et al.  Assignment of Early Caudal Identity to Neural Plate Cells by a Signal from Caudal Paraxial Mesoderm , 1997, Neuron.

[17]  Andrew P. McMahon,et al.  Engrailed-1 as a target of the Wnt-1 signalling pathway in vertebrate midbrain development , 1996, Nature.

[18]  A. McMahon,et al.  Combinatorial signaling by Sonic hedgehog and Wnt family members induces myogenic bHLH gene expression in the somite. , 1995, Genes & development.

[19]  R. Beddington,et al.  Wnt signaling in Xenopus embryos inhibits bmp4 expression and activates neural development. , 1999, Genes & development.

[20]  S. Sokol,et al.  Regulation of Wnt/LRP Signaling by Distinct Domains of Dickkopf Proteins , 2002, Molecular and Cellular Biology.

[21]  R. Wallace,et al.  Protein incorporation by isolated amphibian oocytes III. Optimum incubation conditions , 1973 .

[22]  N. Perrimon,et al.  Differential Recruitment of Dishevelled Provides Signaling Specificity in the Planar Cell Polarity and Wingless Signaling Pathways in Drosophila, Planar Cell Polarity (pcp) Signaling Is Mediated by the Receptor Frizzled (fz) and Transduced by Dishevelled (dsh). Wingless (wg) Signaling Also Requires , 2022 .

[23]  T. Doniach Planar and vertical induction of anteroposterior pattern during the development of the amphibian central nervous system. , 1993, Journal of neurobiology.

[24]  E. D. De Robertis,et al.  A direct screen for secreted proteins in Xenopus embryos identifies distinct activities for the Wnt antagonists Crescent and Frzb-1 , 2000, Mechanisms of Development.

[25]  R. Harland,et al.  Injected Xwnt-8 RNA acts early in Xenopus embryos to promote formation of a vegetal dorsalizing center , 1991, Cell.

[26]  M. Deardorff,et al.  Regulation of eye development by frizzled signaling in Xenopus , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[27]  C. Marcelle,et al.  Ectodermal Wnt Function as a Neural Crest Inducer , 2002, Science.

[28]  Christof Niehrs,et al.  Kremen2 modulates Dickkopf2 activity during Wnt/LRP6 signaling. , 2003, Gene.

[29]  C. Tabin,et al.  Control of dorsoventral somite patterning by Wnt-1 and beta-catenin. , 1998, Developmental biology.

[30]  J. D. Brown,et al.  Expression of a dominant-negative Wnt blocks induction of MyoD in Xenopus embryos. , 1996, Genes & development.

[31]  D. Galas,et al.  Bone dysplasia sclerosteosis results from loss of the SOST gene product, a novel cystine knot-containing protein. , 2001, American journal of human genetics.

[32]  M. Dickinson,et al.  Dorsalization of the neural tube by the non-neural ectoderm. , 1995, Development.

[33]  Scott E. Fraser,et al.  Dishevelled controls cell polarity during Xenopus gastrulation , 2000, Nature.

[34]  D. Melton,et al.  Vertebrate Embryonic Cells Will Become Nerve Cells Unless Told Otherwise , 1997, Cell.

[35]  Michael Kühl,et al.  Head inducer Dickkopf-1 is a ligand for Wnt coreceptor LRP6 , 2001, Current Biology.

[36]  A. Hemmati-Brivanlou,et al.  Caudalization of neural fate by tissue recombination and bFGF. , 1995, Development.

[37]  B. Neel,et al.  Specific modulation of ectodermal cell fates in Xenopus embryos by glycogen synthase kinase. , 1995, Development.

[38]  S. Sokol Analysis of Dishevelled signalling pathways during Xenopus development , 1996, Current Biology.

[39]  J. Mccoy,et al.  Different activities of the frizzled-related proteins frzb2 and sizzled2 during Xenopus anteroposterior patterning. , 2000, Developmental biology.

[40]  R. Krumlauf,et al.  Riding the Crest of the Wnt Signaling Wave , 2002, Science.

[41]  P. Bork The modular architecture of a new family of growth regulators related to connective tissue growth factor , 1993, FEBS letters.

[42]  R. Krumlauf,et al.  Initiation of Rhombomeric Hoxb4 Expression Requires Induction by Somites and a Retinoid Pathway , 1998, Neuron.

[43]  D. Melton,et al.  Inhibition of activin receptor signaling promotes neuralization in Xenopus , 1994, Cell.

[44]  William C. Smith,et al.  Expression cloning of noggin, a new dorsalizing factor localized to the Spemann organizer in Xenopus embryos , 1992, Cell.

[45]  Douglas A. Melton,et al.  Injected Wnt RNA induces a complete body axis in Xenopus embryos , 1991, Cell.

[46]  R. Moon,et al.  Wnt and FGF pathways cooperatively pattern anteroposterior neural ectoderm in Xenopus , 1997, Mechanisms of Development.

[47]  Dianqing Wu,et al.  Second Cysteine-rich Domain of Dickkopf-2 Activates Canonical Wnt Signaling Pathway via LRP-6 Independently of Dishevelled* , 2002, The Journal of Biological Chemistry.

[48]  Yan Li,et al.  LDL-receptor-related protein 6 is a receptor for Dickkopf proteins , 2001, Nature.

[49]  Robert Geisler,et al.  Silberblick/Wnt11 mediates convergent extension movements during zebrafish gastrulation , 2000, Nature.

[50]  S. Sokol,et al.  Axis determination by inhibition of Wnt signaling in Xenopus. , 1999, Genes & development.

[51]  C. Niehrs,et al.  A morphogen gradient of Wnt/beta-catenin signalling regulates anteroposterior neural patterning in Xenopus. , 2001, Development.

[52]  N. Ueno,et al.  A truncated bone morphogenetic protein receptor affects dorsal-ventral patterning in the early Xenopus embryo. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[53]  J. Smith,et al.  Xwnt11 is a target of Xenopus Brachyury: regulation of gastrulation movements via Dishevelled, but not through the canonical Wnt pathway. , 2000, Development.

[54]  C. Niehrs,et al.  Head induction by simultaneous repression of Bmp and Wnt signalling in Xenopus , 1997, Nature.

[55]  T. Jessell,et al.  Dorsal differentiation of neural plate cells induced by BMP-mediated signals from epidermal ectoderm , 1995, Cell.

[56]  Christof Niehrs,et al.  Mutual antagonism between dickkopf1 and dickkopf2 regulates Wnt/β-catenin signalling , 2000, Current Biology.

[57]  R. Krumlauf,et al.  Plasticity in mouse neural crest cells reveals a new patterning role for cranial mesoderm , 2000, Nature Cell Biology.

[58]  R. Moon,et al.  A beta-catenin/XTcf-3 complex binds to the siamois promoter to regulate dorsal axis specification in Xenopus. , 1997, Genes & development.

[59]  Yoichi Kato,et al.  LDL-receptor-related proteins in Wnt signal transduction , 2000, Nature.

[60]  R. Evans,et al.  An essential role for retinoid signaling in anteroposterior neural patterning. , 1997, Development.

[61]  R. Moon,et al.  Interactions between Xwnt-8 and Spemann organizer signaling pathways generate dorsoventral pattern in the embryonic mesoderm of Xenopus. , 1993, Genes & development.

[62]  R. Krumlauf,et al.  Reprogramming Hox Expression in the Vertebrate Hindbrain: Influence of Paraxial Mesoderm and Rhombomere Transposition , 1996, Neuron.

[63]  J. Nathans,et al.  Biochemical characterization of Wnt-frizzled interactions using a soluble, biologically active vertebrate Wnt protein. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[64]  R. Harland,et al.  Fibroblast growth factor is a direct neural inducer, which combined with noggin generates anterior-posterior neural pattern. , 1995, Development.

[65]  I. Dominguez,et al.  Role of glycogen synthase kinase 3 beta as a negative regulator of dorsoventral axis formation in Xenopus embryos. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[66]  H. Varmus,et al.  Regulation of dorsal fate in the neuraxis by Wnt-1 and Wnt-3a. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[67]  J. Slack,et al.  eFGF, Xcad3 and Hox genes form a molecular pathway that establishes the anteroposterior axis in Xenopus. , 1996, Development.

[68]  R. Moon,et al.  Specification of the anteroposterior neural axis through synergistic interaction of the Wnt signaling cascade with noggin and follistatin. , 1995, Developmental biology.

[69]  S. Sokol Mesoderm formation in Xenopus ectodermal explants overexpressing Xwnt8: evidence for a cooperating signal reaching the animal pole by gastrulation. , 1993, Development.

[70]  M. Bronner‐Fraser,et al.  Neural crest induction in Xenopus: evidence for a two-signal model. , 1998, Development.