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Fig. 6. {Delta}Ebf acts as a dominant-negative mutant and impairs neuronal differentiation. (A-D) Flat-mounted hindbrains from chick embryos that were not electroporated (A) or were co-electroporated at stage HH10 with the indicated constructs (B-D) and the GFP expression vector, then collected 24 hours later and processed for neurofilaments immunochemistry. The examples shown are representative of more than 90% of the embryos, from six independent experiments, each involving at least eight embryos. (E-H) Transverse sections from stage HH15 embryos that were co-electroporated with {Delta}Ebf and GFP expression vectors, collected 30 hours later and processed for whole-mount in situ hybridisation with CRABPI (E), Islet1 (F), Ngn2 (G) and NeuroM (H) probes. The cases shown are representative of more than 80% of the embryos, from four independent experiments, each involving at least eight embryos per probe. Electroporation was on the right side. Note that {Delta}Ebf blocks neurofilament induction promoted by Ebf1 and reduces the level of late (CRABPI, Islet), but not early (Ngn2, NeuroM), neurogenesis markers.





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