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Publication : Mouse Ripply2 is downstream of Wnt3a and is dynamically expressed during somitogenesis.

First Author  Biris KK Year  2007
Journal  Dev Dyn Volume  236
Issue  11 Pages  3167-72
PubMed ID  17937396 Mgi Jnum  J:125766
Mgi Id  MGI:3759905 Doi  10.1002/dvdy.21342
Citation  Biris KK, et al. (2007) Mouse Ripply2 is downstream of Wnt3a and is dynamically expressed during somitogenesis. Dev Dyn 236(11):3167-72
abstractText  Somites are blocks of mesoderm that form when segment boundaries are periodically generated in the anterior presomitic mesoderm (PSM). Periodicity is thought to be driven by an oscillating Notch-centered segmentation clock, whereas boundaries are spatially positioned by the secreted signaling molecules Wnt3a and Fgf8. We identified the putative transcriptional corepressor Ripply2 as a differentially expressed gene in wild-type and Wnt3a(-/-) embryos. Here, we show that Ripply2 is expressed in the anterior PSM and that it indeed lies downstream of Wnt3a. Dynamic Ripply2 expression in prospective somites S0 and S-I overlaps with the rostral expression of cycling genes in the Notch pathway, suggesting that Ripply2 may be controlled by the segmentation clock. Continued expression of Ripply2 in embryos lacking Hes7, a molecular oscillator in the Notch clock, indicates that Hes7 is not a major regulator of Ripply2. Our data are consistent with Ripply2 functioning as a segment boundary determination gene during mammalian embryogenesis. Developmental Dynamics 236:3167-3172, 2007. Published 2007 Wiley-Liss, Inc.
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