Wnt signalling required for expansion of neural crest and CNS progenitors

Makoto Ikeya, Scott M. K. Lee, Jane E. Johnson, Andrew P. McMahon () and Shinji Takada ()
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Makoto Ikeya: Centre for Molecular and Developmental Biology, Faculty of Science, Kyoto University, Kitashirakawa
Scott M. K. Lee: The Biolabs, Harvard University
Jane E. Johnson: Cell Biology and Neuroscience, University of Texas Southwestern Medical Center
Andrew P. McMahon: The Biolabs, Harvard University
Shinji Takada: Centre for Molecular and Developmental Biology, Faculty of Science, Kyoto University, Kitashirakawa

Nature, 1997, vol. 389, issue 6654, 966-970

Abstract: Abstract Interactions between cells help to elaborate pattern within the vertebrate central nervous system (CNS)1. The genes Wnt-1 and Wnt-3a, which encode members of the Wnt family of cysteine-rich secreted signals, are coexpressed at the dorsal midline of the developing neural tube, coincident with dorsal patterning2,3. Each signal is essential for embryonic development, Wnt-1 for midbrain patterning4,5 and Wnt-3a for formation of the paraxial mesoderm6, but the absence of a dorsal neural-tube phenotype in each mutant suggests that Wnt signalling may be redundant. Here we demonstrate that in the absence of both Wnt-1 and Wnt-3a there is a marked deficiency in neural crest derivatives, which originate from the dorsal neural tube7, and a pronounced reduction in dorsolateral neural precursors within the neural tube itself. These phenotypes do not seem to result from a disruption in the mechanisms responsible for establishing normal dorsoventral polarity. Rather, our results are consistent with a model in which local Wnt signalling regulates the expansion of dorsal neural precursors. Given the widespread expression of different Wnt genes in discrete areas of the mammalian neural tube3, this may represent a general model for the action of Wnt signalling in the developing CNS.

Date: 1997
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DOI: 10.1038/40146

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