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

• miR-302 is required for neural tube closure and embryonic survival
• miR-302 loss results in increased proliferation of neural progenitors
• miR-302 loss leads to precocious neuronal differentiation
• miR-290 and miR-302 act redundantly early in development

SummaryThe 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.

Graphical AbstractFigure optionsDownload as PowerPoint slide