DNA methyltransferase 3B regulates duration of neural crest production via repression of Sox10

Proc Natl Acad Sci U S A. 2014 Dec 16;111(50):17911-6. doi: 10.1073/pnas.1318408111. Epub 2014 Dec 1.

Abstract

Neural crest stem cells arise within the central nervous system but then undergo an epithelial-to-mesenchymal transition to migrate away and contribute to the peripheral nervous system and craniofacial skeleton. Here we show that DNA methyltransferase 3B (DNMT3B) is responsible for the loss of competence of dorsal neural tube cells to generate emigrating neural crest cells. DNMT3B knockdown results in up-regulation of neural crest markers, prolonged neural crest emigration, and subsequent precocious neuronal differentiation of the trigeminal ganglion. We find that DNMT3B binds to the promoter of Sox10, known to be important for neural crest emigration and lineage acquisition. Bisulfite sequencing further reveals methylation of the Sox10 promoter region upon cessation of emigration in normal embryos, whereas this mark is reduced after DNMT3B loss. Taken together, these results reveal the importance of DNA methylation in regulating the ability of neural tube cells to produce neural crest cells and the timing of peripheral neuron differentiation.

Keywords: DNA methylation; DNMT3B; Sox10; epigenetic; neural crest.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Base Sequence
  • Chick Embryo
  • Chromatin Immunoprecipitation
  • DNA (Cytosine-5-)-Methyltransferases / genetics
  • DNA (Cytosine-5-)-Methyltransferases / metabolism*
  • DNA Methylation / physiology*
  • DNA Methyltransferase 3B
  • Electroporation
  • Epithelial-Mesenchymal Transition / genetics
  • Epithelial-Mesenchymal Transition / physiology
  • Gene Expression Regulation, Developmental / genetics
  • Gene Expression Regulation, Developmental / physiology*
  • Immunohistochemistry
  • In Situ Hybridization
  • Molecular Sequence Data
  • Neural Crest / cytology
  • Neural Crest / embryology*
  • Promoter Regions, Genetic / genetics
  • SOXE Transcription Factors / metabolism*
  • Sequence Analysis, DNA

Substances

  • SOXE Transcription Factors
  • DNA (Cytosine-5-)-Methyltransferases