Abstract

Hox mediated neuroblast apoptosis is a prevalent way to pattern larval central nervous system (CNS) by different Hox genes, but the mechanism of this apoptosis is not understood. Our studies with Abdominal-A (Abd-A) mediated larval neuroblast (pNB) apoptosis suggests that AbdA, its cofactor Extradenticle (Exd), a helix-loop-helix transcription factor Grainyhead (Grh), and Notch signaling transcriptionally contribute to expression of RHG family of apoptotic genes. We find that Grh, AbdA, and Exd function together at multiple motifs on the apoptotic enhancer. In vivo mutagenesis of these motifs suggest that they are important for the maintenance of the activity of the enhancer rather than its initiation. We also find that Exd function is independent of its known partner homothorax in this apoptosis. We extend some of our findings to Deformed expressing region of sub-esophageal ganglia where pNBs undergo a similar Hox dependent apoptosis. We propose a mechanism where common players like Exd-Grh-Notch work with different Hox genes through region specific enhancers to pattern respective segments of larval central nervous system.

Highlights

  • Apoptosis is used to eliminate defective and/or dispensable cell types during development of an organism

  • We find that different Hox genes use a combination of common players (Extradenticle, Grainyhead and Notch) but employ region specific enhancers to cause progenitor cell death in different segments of developing central nervous system

  • Our experiments suggest that AbdA, Exd, Grh and Notch transcriptionally contribute to regulation of RHG genes, and Exd has a Hth independent role in this apoptosis

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Summary

Introduction

Apoptosis is used to eliminate defective and/or dispensable cell types during development of an organism. Hox genes pattern CNS by regulating proliferation, differentiation and apoptosis of different cell types [15,16,17,18,19,20,21,22] [23,24]. Their role in developmental apoptosis of CNS has been reported earlier, both in Drosophila [16,17,18] as well as in vertebrates [21,22], but the molecular mechanism of the cell death in neural stem cells as well as their progeny are not known

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