NeuroD1 reprograms chromatin and transcription factor landscapes to induce the neuronal program.

Kegg Pathway, D R G Drg, Abhijeet Pataskar, Johannes Jung, Pawel Smialowski, Florian Noack, Federico Calegari, Tobias Straub, Vijay K Tiwari

Research output: Contribution to journalArticlepeer-review

85 Citations (Scopus)

Abstract

Cell fate specification relies on the action of critical transcription factors that become available at distinct stages of embryonic development. One such factor is NeuroD1, which is essential for eliciting the neuronal development program and possesses the ability to reprogram other cell types into neurons. Given this capacity, it is important to understand its targets and the mechanism underlying neuronal specification. Here, we show that NeuroD1 directly binds regulatory elements of neuronal genes that are developmentally silenced by epigenetic mechanisms. This targeting is sufficient to initiate events that confer transcriptional competence, including reprogramming of transcription factor landscape, conversion of heterochromatin to euchromatin, and increased chromatin accessibility, indicating potential pioneer factor ability of NeuroD1. The transcriptional induction of neuronal fate genes is maintained via epigenetic memory despite a transient NeuroD1 induction during neurogenesis. NeuroD1 also induces genes involved in the epithelial-to-mesenchymal transition, thereby promoting neuronal migration. Our study not only reveals the NeuroD1-dependent gene regulatory program driving neurogenesis but also increases our understanding of how cell fate specification during development involves a concerted action of transcription factors and epigenetic mechanisms.
Original languageEnglish
Pages (from-to)1-22
Number of pages22
JournalThe EMBO Journal
DOIs
Publication statusPublished - 2015

Keywords

  • epigenetics
  • functional
  • gene regulation
  • genomics
  • neurod 1
  • neurogenesis
  • neuroscience
  • pioneer
  • subject categories chromatin
  • transcription
  • transcription factor

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