Please use this identifier to cite or link to this item: https://doi.org/10.1126/scisignal.2000740
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dc.titleThe Drosophila female germline stem cell lineage acts to spatially restrict DPP function within the niche
dc.contributor.authorLiu, M.
dc.contributor.authorLim, T.M.
dc.contributor.authorCai, Y.
dc.date.accessioned2014-10-27T08:42:10Z
dc.date.available2014-10-27T08:42:10Z
dc.date.issued2010-07-27
dc.identifier.citationLiu, M., Lim, T.M., Cai, Y. (2010-07-27). The Drosophila female germline stem cell lineage acts to spatially restrict DPP function within the niche. Science Signaling 3 (132) : ra57-. ScholarBank@NUS Repository. https://doi.org/10.1126/scisignal.2000740
dc.identifier.issn19450877
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/101894
dc.description.abstractMaintenance of stem cells requires spatially restricted, niche-associated signals. In the Drosophila female germline stem cell (GSC) niche, Decapentaplegic (DPP) is the primary niche-associated factor and functions over a short range to promote GSC self-renewal rather than differentiation. Here, we show that the GSC lineage and, more specifically, the stem cells themselves participate in the spatial restriction of DPP function by activating epidermal growth factor receptor (EGFR)-mitogen-activated protein kinase (MAPK) signaling in the surrounding somatic cells. EGFR-MAPK signaling in somatic cells repressed the expression of dally, which encodes a glypican required for DPP movement and stability. Consequently, only GSCs close to the DPP source (the somatic cells in the niche) showed high signal activation and were maintained as stem cells, whereas cystoblasts outside the niche showed low signal activation and initiated differentiation. Thus, our data reveal that the reciprocal cross talk between the GSCs and the somatic cells defines the spatial limits of DPP action and therefore the extent of the GSC niche. Copyright 2008 by the American Association for the Advancement of Science; all rights reserved.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1126/scisignal.2000740
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentBIOLOGICAL SCIENCES
dc.description.doi10.1126/scisignal.2000740
dc.description.sourcetitleScience Signaling
dc.description.volume3
dc.description.issue132
dc.description.pagera57-
dc.identifier.isiut000280403500003
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