The family of Wnt genes consists of at least 19 members in vertebrates. Wnts have multiple roles during normal development and aetiology of diseases (Wodarz and Nusse 1998; Moon et al. 2002, 2004). These genes encode for glycoproteins that are released in the intercellular space, acting as intercellular mediators (Moon et al. 1997). By binding to their special receptors, the Frizzled (Fz) receptors, they are able to activate at least three different pathways: the canonical, the non-canonical and the Ca2+ pathway (Fig. 1 ). The Wnt family has been subdivided, using functional assays, into at least two subclasses. In Xenopus, Wnt1, Wnt3a and Wnt8 are able to induce axis duplication in embryos, whereas Wnt4, Wnt5a and Wnt11 cannot (Du et al. 1995). Those Wnts that are able to induce axis duplication are thought to act canonically; those who cannot are thought to act non-canonically. In the literature, therefore, some Wnts are called canonical Wnts while others are called noncanonical Wnts, suggesting that a special Wnt always activates the same signalling pathway. It is unlikely that the specificity dictating cellular responses resides solely in the Wnt ligands because no one has reported sequence or structural motifs in Wnts that predict their activities in these cellular and embryonic assays. Further evidence showing that cellular responses cannot be predicted based solely on the identity of the Wnt comes from the finding that the “non-canonical” Wnt5 is able to induce axis duplication and stabilisation of β-catenin if some Fz receptors are also present; in other words, it is able to act canonically (He et al. 1997; Kühl et al. 2000). We should therefore act on the assumption that any Wnt is able to activate different signalling pathways depending on the expression of Fz receptors and on the presence of different signal-interfering molecules in the cellular environment.
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© 2008 Springer-Verlag Berlin Heidelberg
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(2008). Introduction. In: The Role of Wnt Signalling in the Development of Somites and Neural Crest. Advances in Anatomy Embryology and Cell Biology, vol 195. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-540-77727-4_1
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