A temporal mechanism that produces neuronal diversity in the Drosophila visual center

Dev Biol. 2013 Aug 1;380(1):12-24. doi: 10.1016/j.ydbio.2013.05.002. Epub 2013 May 9.

Abstract

The brain consists of various types of neurons that are generated from neural stem cells; however, the mechanisms underlying neuronal diversity remain uncertain. A recent study demonstrated that the medulla, the largest component of the Drosophila optic lobe, is a suitable model system for brain development because it shares structural features with the mammalian brain and consists of a moderate number and various types of neurons. The concentric zones in the medulla primordium that are characterized by the expression of four transcription factors, including Homothorax (Hth), Brain-specific homeobox (Bsh), Runt (Run) and Drifter (Drf), correspond to types of medulla neurons. Here, we examine the mechanisms that temporally determine the neuronal types in the medulla primordium. For this purpose, we searched for transcription factors that are transiently expressed in a subset of medulla neuroblasts (NBs, neuronal stem cell-like neural precursor cells) and identified five candidates (Hth, Klumpfuss (Klu), Eyeless (Ey), Sloppy paired (Slp) and Dichaete (D)). The results of genetic experiments at least explain the temporal transition of the transcription factor expression in NBs in the order of Ey, Slp and D. Our results also suggest that expression of Hth, Klu and Ey in NBs trigger the production of Hth/Bsh-, Run- and Drf-positive neurons, respectively. These results suggest that medulla neuron types are specified in a birth order-dependent manner by the action of temporal transcription factors that are sequentially expressed in NBs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Animals
  • Brain / embryology*
  • Cell Differentiation
  • Crosses, Genetic
  • Drosophila melanogaster / embryology*
  • Gene Expression Regulation, Developmental*
  • Green Fluorescent Proteins / metabolism
  • Mutation
  • Neurons / metabolism
  • Neurons / physiology*
  • Optic Lobe, Nonmammalian / embryology*
  • Time Factors
  • Transcription Factors / metabolism

Substances

  • Transcription Factors
  • Green Fluorescent Proteins