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pubmed-article:17937396pubmed:abstractTextSomites 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. Developmentallld:pubmed
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pubmed-article:17937396pubmed:copyrightInfoPublished 2007 Wiley-Liss, Inc.lld:pubmed
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pubmed-article:17937396pubmed:volume236lld:pubmed
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pubmed-article:17937396pubmed:pagination3167-72lld:pubmed
pubmed-article:17937396pubmed:dateRevised2011-11-17lld:pubmed
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pubmed-article:17937396pubmed:articleTitleMouse Ripply2 is downstream of Wnt3a and is dynamically expressed during somitogenesis.lld:pubmed
pubmed-article:17937396pubmed:affiliationCancer and Developmental Biology Laboratory, Center for Cancer Research, NCI-Frederick, NIH, Frederick, Maryland 21702, USA.lld:pubmed
pubmed-article:17937396pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:17937396pubmed:publicationTypeResearch Support, N.I.H., Intramurallld:pubmed
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