trying... 1754434120071107200708131567-133X772007AugGene expression patterns : GEPGene Expr PatternsExpression patterns of chick Musashi-1 in the developing nervous system.817825817-25Vertebrate homologues of musashi have recently been referred to as neural stem cell markers because of their expression patterns and RNA-binding interactions. In the context of the notch signaling pathway, Musashi-1 (Msi-1) is a regulator of neural cell generation, cooperating with notch to maintain mitosis. In an effort to identify definitive stem cell markers of the neural retina, a portion of the Msi-1 cDNA was cloned, and the expression of Msi-1 in the chick eye was analyzed. Using an Msi-1-specific antibody and RNA probe, we show that expression of Msi-1 in the early neural tube is consistent with neural stem identity. In the neural retina, expression starts shortly before embryonic day 3 (E3) and continues up to and including E18. A BrdU incorporation assay shows Msi-1 to be found in both proliferating and differentiating cells of E5 neural retina. At E8 (when proliferation is complete in the fundus of the retina) and E18 (mature retina) Msi-1 expression was found in the ciliary marginal zone (CMZ) as well as in a subpopulation of differentiated cells, including photoreceptors and ganglion cells.WilsonJonathan MJMDepartment of Biology and Center for Regenerative Biology and Medicine, Indiana University-Purdue University Indianapolis, Indianapolis, IN 46202, USA.SatoKazunaKChernoffEllen A GEABelecky-AdamsTeri LTLengJournal ArticleResearch Support, Non-U.S. Gov't20070421NetherlandsGene Expr Patterns1011674731567-133X0Eye Proteins0Nerve Tissue Proteins0Receptors, Notch0Repressor ProteinsIMAnimalsCell ProliferationChick EmbryoComputational BiologyEyeembryologyEye ProteinsbiosynthesisGene Expression ProfilingGene Expression Regulation, DevelopmentalNerve Tissue ProteinsbiosynthesisNervous SystemembryologyNeuronsmetabolismReceptors, NotchmetabolismRepressor ProteinsbiosynthesisRetinametabolismSignal TransductionStem CellsmetabolismTime Factors20061220200732620074152007659020071189020076590ppublish1754434110.1016/j.modgep.2007.04.001S1567-133X(07)00044-0trying2... trying... 14467501MCID_676f08612395b5e646060b403971969439710099397058083970266839700141neural"neural"[All Fields] OR "neuralization"[All Fields] OR "neuralize"[All Fields] OR "neuralized"[All Fields] OR "neuralizes"[All Fields] OR "neuralizing"[All Fields] OR "neurally"[All Fields]retina"retina"[MeSH Terms] OR "retina"[All Fields] OR "retinas"[All Fields] OR "retina's"[All Fields] OR "retinae"[All Fields]("neural"[All Fields] OR "neuralization"[All Fields] OR "neuralize"[All Fields] OR "neuralized"[All Fields] OR "neuralizes"[All Fields] OR "neuralizing"[All Fields] OR "neurally"[All Fields]) AND ("retina"[MeSH Terms] OR "retina"[All Fields] OR "retinas"[All Fields] OR "retina s"[All Fields] OR "retinae"[All Fields])
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Expression patterns of chick Musashi-1 in the developing nervous system. | LitMetric
Vertebrate homologues of musashi have recently been referred to as neural stem cell markers because of their expression patterns and RNA-binding interactions. In the context of the notch signaling pathway, Musashi-1 (Msi-1) is a regulator of neural cell generation, cooperating with notch to maintain mitosis. In an effort to identify definitive stem cell markers of the neural retina, a portion of the Msi-1 cDNA was cloned, and the expression of Msi-1 in the chick eye was analyzed. Using an Msi-1-specific antibody and RNA probe, we show that expression of Msi-1 in the early neural tube is consistent with neural stem identity. In the neural retina, expression starts shortly before embryonic day 3 (E3) and continues up to and including E18. A BrdU incorporation assay shows Msi-1 to be found in both proliferating and differentiating cells of E5 neural retina. At E8 (when proliferation is complete in the fundus of the retina) and E18 (mature retina) Msi-1 expression was found in the ciliary marginal zone (CMZ) as well as in a subpopulation of differentiated cells, including photoreceptors and ganglion cells.