Control of neural crest multipotency by Wnt signaling and the Lin28/ let-7 axis

Elife. 2018 Dec 6:7:e40556. doi: 10.7554/eLife.40556.

Abstract

A crucial step in cell differentiation is the silencing of developmental programs underlying multipotency. While much is known about how lineage-specific genes are activated to generate distinct cell types, the mechanisms driving suppression of stemness are far less understood. To address this, we examined the regulation of the transcriptional network that maintains progenitor identity in avian neural crest cells. Our results show that a regulatory circuit formed by Wnt, Lin28a and let-7 miRNAs controls the deployment and the subsequent silencing of the multipotency program in a position-dependent manner. Transition from multipotency to differentiation is determined by the topological relationship between the migratory cells and the dorsal neural tube, which acts as a Wnt-producing stem cell niche. Our findings highlight a mechanism that rapidly silences complex regulatory programs, and elucidate how transcriptional networks respond to positional information during cell differentiation.

Keywords: Lin28; Neural crest; Wnt singling; chicken; developmental biology; gene regulatory networks; multipotency; stem cell.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Avian Proteins / genetics*
  • Avian Proteins / metabolism
  • Cell Differentiation
  • Cell Movement
  • Chick Embryo
  • Forkhead Transcription Factors / genetics
  • Forkhead Transcription Factors / metabolism
  • Gene Expression Regulation, Developmental*
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism
  • Morpholinos / genetics
  • Morpholinos / metabolism
  • Multipotent Stem Cells / cytology
  • Multipotent Stem Cells / metabolism
  • Neural Crest / cytology
  • Neural Crest / growth & development
  • Neural Crest / metabolism*
  • Neurons / cytology
  • Neurons / metabolism*
  • Neuropeptides / biosynthesis
  • Neuropeptides / genetics
  • PAX7 Transcription Factor / genetics
  • PAX7 Transcription Factor / metabolism
  • Proto-Oncogene Proteins c-myc / genetics
  • Proto-Oncogene Proteins c-myc / metabolism
  • RNA-Binding Proteins / genetics
  • RNA-Binding Proteins / metabolism
  • SOXE Transcription Factors / genetics
  • SOXE Transcription Factors / metabolism
  • Transcription, Genetic
  • Wnt Proteins / antagonists & inhibitors
  • Wnt Proteins / genetics*
  • Wnt Proteins / metabolism
  • Wnt Signaling Pathway
  • Zinc Fingers / genetics*

Substances

  • Avian Proteins
  • Forkhead Transcription Factors
  • MicroRNAs
  • Morpholinos
  • Neuropeptides
  • PAX7 Transcription Factor
  • Proto-Oncogene Proteins c-myc
  • RNA-Binding Proteins
  • SOXE Transcription Factors
  • Wnt Proteins