| Literature DB >> 19906847 |
A Burcu Babaoglan1, Kate M O'Connor-Giles, Hemlata Mistry, Adam Schickedanz, Beth A Wilson, James B Skeath.
Abstract
Asymmetric cell divisions generate sibling cells of distinct fates ('A', 'B') and constitute a fundamental mechanism that creates cell-type diversity in multicellular organisms. Antagonistic interactions between the Notch pathway and the intrinsic cell-fate determinant Numb appear to regulate asymmetric divisions in flies and vertebrates. During these divisions, productive Notch signaling requires sanpodo, which encodes a novel transmembrane protein. Here, we demonstrate that Drosophila sanpodo plays a dual role to regulate Notch signaling during asymmetric divisions - amplifying Notch signaling in the absence of Numb in the 'A' daughter cell and inhibiting Notch signaling in the presence of Numb in the 'B' daughter cell. In so doing, sanpodo ensures the asymmetry in Notch signaling levels necessary for the acquisition of distinct fates by the two daughter cells. These findings answer long-standing questions about the restricted ability of Numb and Sanpodo to inhibit and to promote, respectively, Notch signaling during asymmetric divisions.Entities:
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Year: 2009 PMID: 19906847 PMCID: PMC2781049 DOI: 10.1242/dev.040386
Source DB: PubMed Journal: Development ISSN: 0950-1991 Impact factor: 6.868