| Literature DB >> 16516838 |
Jacqueline Kim Dale1, Pascale Malapert, Jérome Chal, Gonçalo Vilhais-Neto, Miguel Maroto, Teri Johnson, Sachintha Jayasinghe, Paul Trainor, Bernhard Herrmann, Olivier Pourquié.
Abstract
The segmented body plan of vertebrate embryos arises through segmentation of the paraxial mesoderm to form somites. The tight temporal and spatial control underlying this process of somitogenesis is regulated by the segmentation clock and the FGF signaling wavefront. Here, we report the cyclic mRNA expression of Snail 1 and Snail 2 in the mouse and chick presomitic mesoderm (PSM), respectively. Whereas Snail genes' oscillations are independent of NOTCH signaling, we show that they require WNT and FGF signaling. Overexpressing Snail 2 in the chick embryo prevents cyclic Lfng and Meso 1 expression in the PSM and disrupts somite formation. Moreover, cells mis-expressing Snail 2 fail to express Paraxis, remain mesenchymal, and are thereby inhibited from undergoing the epithelialization event that culminates in the formation of the epithelial somite. Thus, Snail genes define a class of cyclic genes that coordinate segmentation and PSM morphogenesis.Entities:
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Year: 2006 PMID: 16516838 DOI: 10.1016/j.devcel.2006.02.011
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270