Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
XB-ART-38654
Dev Dyn June 1, 2009; 238 (6): 1332-45.

In vivo analyzes of dystroglycan function during somitogenesis in Xenopus laevis.

Hidalgo M , Sirour C , Bello V , Moreau N , Beaudry M , Darribère T .


Abstract
Dystroglycan (Dg) is a cell adhesion receptor for laminin that has been reported to play a role in skeletal muscle cell stability, cytoskeletal organization, cell polarity, and signaling. Here we show that Dg is expressed at both the notochord/somite and the intersomitic boundaries, where laminin and fibronectin are accumulated during somitogenesis. Inhibition of Dg function with morpholino antisense oligonucleotides or a dominant negative mutant results in the normal segmentation of the presomitic mesoderm but affects the number, the size, and the integrity of somites. Depletion of Dg disrupts proliferation and alignment of myoblasts without affecting XMyoD and XMRF4 expression. It also leads to defects in laminin deposition at the intersomitic junctions, whereas expression of integrin beta1 subunits and fibronectin assembly occur normally. Our results show that Dg is critical for both proliferation and elongation of somitic cells and that the Dg-cytoplasmic domain is required for the laminin assembly at the intersomitic boundaries. Developmental Dynamics 238:1332-1345, 2009. (c) 2008 Wiley-Liss, Inc.

PubMed ID: 19086027
Article link: Dev Dyn
Grant support: [+]

Species referenced: Xenopus laevis
Genes referenced: dag1 fn1 hopx itgb1 lama1 myf6 myod1
Antibodies: Dag1 Ab2 Fn1 Ab1 H3f3a Ab10 Itgb1 Ab1 Lama1 Ab1 Myf6 Ab1 Myod1 Ab1 Somite Ab1
Morpholinos: dag1 MO1 dag1 MO2


Article Images: [+] show captions