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Multiple roles of mesenchymal beta-catenin during murine limb patterning

Item Type:Article
Title:Multiple roles of mesenchymal beta-catenin during murine limb patterning
Creators Name:Hill, T.P., Taketo, M.M., Birchmeier, W. and Hartmann, C.
Abstract:Recently canonical Wnt signaling in the ectoderm has been shown to be required for maintenance of the apical ectodermal ridge (AER) and for dorsoventral signaling. Using conditional gain- and loss-of-function -catenin alleles, we have studied the role of mesenchymal -catenin activity during limb development. Here, we show that loss of -catenin results in limb truncations due to a defect in AER maintenance. Stabilization of -catenin also results in truncated limbs, caused by a premature regression of the AER. Concomitantly, in these limbs, the expression of Bmp2, Bmp4 and Bmp7, and of the Bmp target genes Msx1, Msx2 and gremlin, is expanded in the mesenchyme. Furthermore, we found that the expression of Lmx1b, a gene exclusively expressed in the dorsal limb mesenchyme and involved in dorsoventral patterning, is reduced upon loss of -catenin activity and is expanded ventrally in gainof- function limbs. However, the known ectodermal regulators Wnt7a and engrailed 1 are expressed normally. This suggests that Lmx1b is also regulated, in part, by a -catenin-mediated Wnt signal, independent of the non-canoncial Wnt7a signaling pathway. In addition, loss of -catenin results in a severe agenesis of the scapula. Concurrently, the expression of two genes, Pax1 and Emx2, which have been implicated in scapula development, is lost in -catenin loss-of-function limbs; however, only Emx2 is upregulated in gain-of-function limbs. Mesenchymal -catenin activity is therefore required for AER maintenance, and for normal expression of Lmx1b and Emx2.
Keywords:AER, Beta-Catenin, BMP, Dorsoventral Axis, Emx2, Limb Patterning, Lmx1b, Scapula, Animals, Mice
Source:Development
ISSN:0950-1991
Publisher:Company of Biologists
Volume:133
Number:7
Page Range:1219-1229
Date:1 April 2006
Official Publication:https://doi.org/10.1242/dev.02298
PubMed:View item in PubMed

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