miR-302 Is Required for Timing of Neural Differentiation, Neural Tube Closure, and Embryonic Viability
Year: 2015
Type: article
Abstract: 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.
Source: Cell Reports
Institution: University of California, San Francisco
Language: English
Subfield: Developmental Neuroscience
Field: Neuroscience
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $5,620
Awards: Origins and Biological Consequences of Human Infertility, Cell Biological Determinants of Jaw Size, MicroRNA Based Pathway Discovery in Cellular Reprogramming, Genetic Studies of Cortex Structure and Development, Center for Research, Innovation and Training in Reproduction and Infertility, Integrated Training in Reproductive Sciences, P0044380 Parchem - Role of Small RNA's in Development, Mesenchymal Regulation of Osteogenesis, G977768287
OpenAlex ID: W1732806884
