Specification of the Drosophila Orcokinin A neurons by combinatorial coding

Cell Tissue Res. 2023 Feb;391(2):269-286. doi: 10.1007/s00441-022-03721-x. Epub 2022 Dec 13.

Abstract

The central nervous system contains a daunting number of different cell types. Understanding how each cell acquires its fate remains a major challenge for neurobiology. The developing embryonic ventral nerve cord (VNC) of Drosophila melanogaster has been a powerful model system for unraveling the basic principles of cell fate specification. This pertains specifically to neuropeptide neurons, which typically are stereotypically generated in discrete subsets, allowing for unambiguous single-cell resolution in different genetic contexts. Here, we study the specification of the OrcoA-LA neurons, characterized by the expression of the neuropeptide Orcokinin A and located laterally in the A1-A5 abdominal segments of the VNC. We identified the progenitor neuroblast (NB; NB5-3) and the temporal window (castor/grainyhead) that generate the OrcoA-LA neurons. We also describe the role of the Ubx, abd-A, and Abd-B Hox genes in the segment-specific generation of these neurons. Additionally, our results indicate that the OrcoA-LA neurons are "Notch Off" cells, and neither programmed cell death nor the BMP pathway appears to be involved in their specification. Finally, we performed a targeted genetic screen of 485 genes known to be expressed in the CNS and identified nab, vg, and tsh as crucial determinists for OrcoA-LA neurons. This work provides a new neuropeptidergic model that will allow for addressing new questions related to neuronal specification mechanisms in the future.

Keywords: CNS development; Cell specification; Drosophila; Hox genes; Orcokinin A.

MeSH terms

  • Animals
  • Drosophila
  • Drosophila Proteins* / genetics
  • Drosophila Proteins* / metabolism
  • Drosophila melanogaster / genetics
  • Gene Expression Regulation, Developmental
  • Homeodomain Proteins / metabolism
  • Neurons / metabolism
  • Neuropeptides* / genetics
  • Neuropeptides* / metabolism
  • Repressor Proteins
  • Transcription Factors / metabolism

Substances

  • orcokinin
  • Drosophila Proteins
  • Neuropeptides
  • Ubx protein, Drosophila
  • Transcription Factors
  • Homeodomain Proteins
  • tsh protein, Drosophila
  • Repressor Proteins

Grants and funding