Neuronal cell fate diversification controlled by sub-temporal action of Kruppel

Elife. 2016 Oct 14:5:e19311. doi: 10.7554/eLife.19311.

Abstract

During Drosophila embryonic nervous system development, neuroblasts express a programmed cascade of five temporal transcription factors that govern the identity of cells generated at different time-points. However, these five temporal genes fall short of accounting for the many distinct cell types generated in large lineages. Here, we find that the late temporal gene castor sub-divides its large window in neuroblast 5-6 by simultaneously activating two cell fate determination cascades and a sub-temporal regulatory program. The sub-temporal program acts both upon itself and upon the determination cascades to diversify the castor window. Surprisingly, the early temporal gene Kruppel acts as one of the sub-temporal genes within the late castor window. Intriguingly, while the temporal gene castor activates the two determination cascades and the sub-temporal program, spatial cues controlling cell fate in the latter part of the 5-6 lineage exclusively act upon the determination cascades.

Keywords: D. melanogaster; cell fate specification; developmental biology; feedforward regulatory pathways; neuroscience; stem cells; temporal changes in competence.

MeSH terms

  • Animals
  • DNA-Binding Proteins / metabolism
  • Drosophila / embryology*
  • Drosophila Proteins / metabolism*
  • Gene Expression Regulation, Developmental*
  • Kruppel-Like Transcription Factors / metabolism*
  • Nervous System / embryology*

Substances

  • DNA-Binding Proteins
  • Drosophila Proteins
  • Kr protein, Drosophila
  • Kruppel-Like Transcription Factors
  • cas protein, Drosophila

Grants and funding

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.