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      Regulation of isthmic Fgf8 signal by sprouty2.

      Development (Cambridge, England)
      Adaptor Proteins, Signal Transducing, Animals, Brain, embryology, Cell Differentiation, Chick Embryo, DNA, Complementary, metabolism, Electroporation, Extracellular Signal-Regulated MAP Kinases, Fibroblast Growth Factor 8, Fibroblast Growth Factors, Gene Expression Regulation, Developmental, Genes, Dominant, Genetic Vectors, Homeodomain Proteins, physiology, Immunohistochemistry, In Situ Hybridization, Intracellular Signaling Peptides and Proteins, Membrane Proteins, Mesencephalon, Metencephalon, Models, Biological, Oligonucleotides, Antisense, chemistry, Proteins, Signal Transduction, ras Proteins

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          Abstract

          Fgf8 functions as an organizer at the mes/metencephalic boundary (isthmus). We showed that a strong Fgf8 signal activates the Ras-ERK signaling pathway to organize cerebellar differentiation. Sprouty2 is expressed in an overlapping manner to Fgf8, and is induced by Fgf8. Its function, however, is indicated to antagonize Ras-ERK signaling. Here, we show the regulation of Fgf8 signaling in relation to Sprouty2. sprouty2 expression was induced very rapidly by Fgf8b, but interfered with ERK activation. sprouty2 misexpression resulted in a fate change of the presumptive metencephalon to the mesencephalon. Misexpression of a dominant negative form of Sprouty2 augmented ERK activation, and resulted in anterior shift of the posterior border of the tectum. The results indicate that Fgf8 activates the Ras-ERK signaling pathway to differentiate the cerebellum, and that the hyper- or hypo-signaling of this pathway affects the fate of the brain vesicles. Sprouty2 may regulate the Fgf8-Ras-ERK signaling pathway for the proper regionalization of the metencephalon and mesencephalon.

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