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Author Notes:

For correspondence: Email: kmoberg@emory.edu, Dept. of Cell Biology, Emory University School of Medicine, 615 Michael Street, Rm 435, Atlanta, GA 30322, USA, and ; Email: smkelly@wooster.edu, Dept. of Biology, College of Wooster, 1189 Beall Avenue, Wooster, Ohio 44691

We thank the Bloomington Drosophila Stock Center (Indiana, USA) and Developmental Studies Hybridoma Bank (Iowa, USA) for providing stocks and antibodies, and members of the Moberg, Kelly, and Corbett laboratories and S. Sanyal for helpful discussions and advice.

The authors declare no competing financial interests

Subjects:

Research Funding:

Financial support as follows - NIH 5K12 GM000680-12 (SMK), NIH F31 HD079226 (RB), and NIH MH107305 and GM058728 (AHC and KHM).

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Developmental Biology
  • Neurosciences
  • Neurosciences & Neurology
  • Drosophila
  • mushroom body development
  • polyadenosine RNA binding protein
  • dNab2
  • MENTAL-RETARDATION PROTEIN
  • MUSHROOM BODY DEVELOPMENT
  • REPRESSIBLE CELL MARKER
  • POLYADENOSINE RNA
  • MOSAIC ANALYSIS
  • BODIES
  • GUIDANCE
  • DSCAM
  • MORPHOGENESIS
  • NEUROTOXICITY

The Drosophila ortholog of the Zc3h14 RNA binding protein acts within neurons to pattern axon projection in the developing brain

Journal Title:

Developmental Neurobiology

Volume:

Volume 76, Number 1

Publisher:

, Pages 93-106

Type of Work:

Article | Post-print: After Peer Review

Abstract:

The dNab2 polyadenosine RNA binding protein is the D. melanogaster ortholog of the vertebrate ZC3H14 protein, which is lost in a form of inherited intellectual disability (ID). Human ZC3H14 can rescue D. melanogaster dNab2 mutant phenotypes when expressed in all neurons of the developing nervous system, suggesting that dNab2/ZC3H14 performs well-conserved roles in neurons. However, the cellular and molecular requirements for dNab2/ZC3H14 in the developing nervous system have not been defined in any organism. Here we show that dNab2 is autonomously required within neurons to pattern axon projection from Kenyon neurons into the mushroom bodies, which are required for associative olfactory learning and memory in insects. Mushroom body axons lacking dNab2 project aberrantly across the brain midline and also show evidence of defective branching. Coupled with the prior finding that ZC3H14 is highly expressed in rodent hippocampal neurons, this requirement for dNab2 in mushroom body neurons suggests that dNab2/ZC3H14 has a conserved role in supporting axon projection and branching. Consistent with this idea, loss of dNab2 impairs short-term memory in a courtship conditioning assay. Taken together these results reveal a cell-autonomous requirement for the dNab2 RNA binding protein in mushroom body development and provide a window into potential neurodevelopmental functions of the human ZC3H14 protein.

Copyright information:

© 2015 Wiley Periodicals, Inc.

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