Nanos-mediated repression of hid protects larval sensory neurons after a global switch in sensitivity to apoptotic signals

Development. 2016 Jun 15;143(12):2147-59. doi: 10.1242/dev.132415. Epub 2016 May 4.

Abstract

Dendritic arbor morphology is a key determinant of neuronal function. Once established, dendrite branching patterns must be maintained as the animal develops to ensure receptive field coverage. The translational repressors Nanos (Nos) and Pumilio (Pum) are required to maintain dendrite growth and branching of Drosophila larval class IV dendritic arborization (da) neurons, but their specific regulatory role remains unknown. We show that Nos-Pum-mediated repression of the pro-apoptotic gene head involution defective (hid) is required to maintain a balance of dendritic growth and retraction in class IV da neurons and that upregulation of hid results in decreased branching because of an increase in caspase activity. The temporal requirement for nos correlates with an ecdysone-triggered switch in sensitivity to apoptotic stimuli that occurs during the mid-L3 transition. We find that hid is required during pupariation for caspase-dependent pruning of class IV da neurons and that Nos and Pum delay pruning. Together, these results suggest that Nos and Pum provide a crucial neuroprotective regulatory layer to ensure that neurons behave appropriately in response to developmental cues.

Keywords: Caspase; Drosophila; Non-apoptotic function; Nos; da neurons; hid.

MeSH terms

  • 3' Untranslated Regions / genetics
  • Animals
  • Apoptosis*
  • Caspases / metabolism
  • Cytoprotection*
  • Dendrites / metabolism
  • Drosophila Proteins / chemistry
  • Drosophila Proteins / metabolism*
  • Ecdysone / metabolism
  • Larva / cytology
  • Larva / metabolism
  • Mitochondria / metabolism
  • Mutation / genetics
  • Neuropeptides / metabolism*
  • Phenotype
  • Protein Binding
  • Pupa / metabolism
  • RNA-Binding Proteins / chemistry
  • RNA-Binding Proteins / metabolism*
  • Sensory Receptor Cells / cytology*
  • Sensory Receptor Cells / metabolism*
  • Signal Transduction*
  • Up-Regulation / genetics

Substances

  • 3' Untranslated Regions
  • Drosophila Proteins
  • HID protein, Drosophila
  • Neuropeptides
  • RNA-Binding Proteins
  • pum protein, Drosophila
  • nos protein, Drosophila
  • Ecdysone
  • Caspases