Control of neural crest multipotency by Wnt signaling and the Lin28/let-7 axis.
Debadrita BhattacharyaMegan RothsteinAna Paula AzambujaMarcos Simoes-CostaPublished in: eLife (2018)
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.
Keyphrases
- stem cells
- induced apoptosis
- transcription factor
- cell cycle arrest
- single cell
- cell proliferation
- gene expression
- public health
- cell therapy
- endoplasmic reticulum stress
- spinal cord
- epithelial mesenchymal transition
- oxidative stress
- cell death
- quality improvement
- dna methylation
- heat shock
- genome wide
- spinal cord injury
- cell fate
- bioinformatics analysis