Mir-29b Mediates the Neural Tube versus Neural Crest Fate Decision during Embryonic Stem Cell Neural Differentiation

Stem Cell Reports. 2017 Aug 8;9(2):571-586. doi: 10.1016/j.stemcr.2017.06.017. Epub 2017 Jul 27.

Abstract

During gastrulation, the neuroectoderm cells form the neural tube and neural crest. The nervous system contains significantly more microRNAs than other tissues, but the role of microRNAs in controlling the differentiation of neuroectodermal cells into neural tube epithelial (NTE) cells and neural crest cells (NCCs) remains unknown. Using embryonic stem cell (ESC) neural differentiation systems, we found that miR-29b was upregulated in NTE cells and downregulated in NCCs. MiR-29b promoted the differentiation of ESCs into NTE cells and inhibited their differentiation into NCCs. Accordingly, the inhibition of miR-29b significantly inhibited the differentiation of NTE cells. A mechanistic study revealed that miR-29b targets DNA methyltransferase 3a (Dnmt3a) to regulate neural differentiation. Moreover, miR-29b mediated the function of Pou3f1, a critical neural transcription factor. Therefore, our study showed that the Pou3f1-miR-29b-Dnmt3a regulatory axis was active at the initial stage of neural differentiation and regulated the determination of cell fate.

Keywords: Dnmt3a; ESCs; Pou3f1; miR-29b; neural crest cells; neural tube epithelial cells.

MeSH terms

  • Animals
  • Biomarkers
  • Cell Differentiation / genetics*
  • Cell Line
  • Cell Lineage / genetics
  • DNA (Cytosine-5-)-Methyltransferases / genetics
  • DNA (Cytosine-5-)-Methyltransferases / metabolism
  • DNA Methyltransferase 3A
  • Embryonic Stem Cells / cytology*
  • Embryonic Stem Cells / metabolism*
  • Gene Expression Regulation
  • Humans
  • Mice
  • MicroRNAs / genetics*
  • Neural Crest / embryology*
  • Neural Crest / metabolism*
  • Neural Tube / embryology*
  • Neural Tube / metabolism*
  • Octamer Transcription Factor-6 / genetics
  • RNA Interference

Substances

  • Biomarkers
  • DNMT3A protein, human
  • Dnmt3a protein, mouse
  • MIRN29a microRNA, human
  • MicroRNAs
  • POU3F1 protein, human
  • Octamer Transcription Factor-6
  • DNA (Cytosine-5-)-Methyltransferases
  • DNA Methyltransferase 3A