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miR-302 Is Required for Timing of Neural Differentiation, Neural Tube Closure, and Embryonic Viability

2015; Cell Press; Volume: 12; Issue: 5 Linguagem: Inglês

10.1016/j.celrep.2015.06.074

2639-1856

Ronald J. Parchem, Nicole Moore, Jennifer L. Fish, Jacqueline G. Parchem, Tárcio Teodoro Braga, Archana Shenoy, Michael C. Oldham, John L.R. Rubenstein, Richard A. Schneider, Robert Blelloch,

RNA Research and Splicing

The evolutionarily conserved miR-302 family of microRNAs is expressed during early mammalian embryonic development. Here, we report that deletion of miR-302a-d in mice results in a fully penetrant late embryonic lethal phenotype. Knockout embryos have an anterior neural tube closure defect associated with a thickened neuroepithelium. The neuroepithelium shows increased progenitor proliferation, decreased cell death, and precocious neuronal differentiation. mRNA profiling at multiple time points during neurulation uncovers a complex pattern of changing targets over time. Overexpression of one of these targets, Fgf15, in the neuroepithelium of the chick embryo induces precocious neuronal differentiation. Compound mutants between mir-302 and the related mir-290 locus have a synthetic lethal phenotype prior to neurulation. Our results show that mir-302 helps regulate neurulation by suppressing neural progenitor expansion and precocious differentiation. Furthermore, these results uncover redundant roles for mir-290 and mir-302 early in development.