Abstract
AbstractDuring development, nervous systems generate an incredible diversity of different cell types. One mechanism that appears critical for controlling whether a specific subtype is present or absent, and ensuring that neuronal numbers are appropriate for specific regions, is programmed cell death.Here we show that the precisely patterned hemilineage-based cell death found in the ventral nerve cord ofDrosophila melanogasteris controlled by the transcription of the pro-apoptotic RHG genesreaperandgrim.Using smFISH we show thatreaperandgrim, but nothid, are expressed in postembryonic lineages during neurogenesis. By generating novel T2A-GAL4 knock-in tools we have been able to mapreaperandgrimexpression on a lineage-by-lineage basis and show diverse expression patterns within different hemilineage populations. Analysis of null mutants for both genes reveal a ‘division of labour’ with distinct combinations being important in sculpting the nervous system.Investigation of a specific sexually dimorphic lineage reveals temporal patterning of hemilineage-specific programmed cell death through Grim and Reaper function underpins the development of sex-specific circuitry in the VNC.Our findings suggest that the precisely patterned expression of these pro-apoptotic genes is a critical fate determinant that generates segmental-specific circuity and instructs the appropriate assembly of sexually dimorphic neural circuits in the VNC.
Publisher
Cold Spring Harbor Laboratory