Differential regulation of dendritic and axonal development by the novel Krüppel-like factor Dar1

J Neurosci. 2011 Mar 2;31(9):3309-19. doi: 10.1523/JNEUROSCI.6307-10.2011.

Abstract

Dendrites and axons are two major neuronal compartments with differences that are critical for neuronal functions. To learn about the differential regulation of dendritic and axonal development, we conducted a genetic screen in Drosophila and isolated the dendritic arbor reduction 1 (dar1) mutants, which display defects in dendritic but not axonal growth. The dar1 gene encodes a novel transcription regulator in the Krüppel-like factor family. Neurons lacking dar1 function have severely reduced growth of microtubule- but not F-actin-based dendritic branches. In contrast, overexpression of Dar1 dramatically increased the growth of microtubule-based dendritic branches. Our results suggest that Dar1 promotes dendrite growth in part by suppressing the expression of the microtubule-severing protein Spastin. Our study thus uncovers a novel transcriptional program for microtubule regulation that preferentially controls dendrite growth.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphatases / antagonists & inhibitors*
  • Adenosine Triphosphatases / biosynthesis
  • Adenosine Triphosphatases / genetics
  • Animals
  • Animals, Genetically Modified
  • Axons / physiology*
  • Axons / ultrastructure
  • Dendrites / physiology*
  • Dendrites / ultrastructure
  • Drosophila Proteins / antagonists & inhibitors*
  • Drosophila Proteins / biosynthesis
  • Drosophila Proteins / deficiency
  • Drosophila Proteins / genetics
  • Drosophila Proteins / physiology*
  • Drosophila melanogaster
  • Female
  • Kruppel-Like Transcription Factors / deficiency
  • Kruppel-Like Transcription Factors / genetics
  • Kruppel-Like Transcription Factors / physiology*
  • Male
  • Receptors, G-Protein-Coupled / deficiency
  • Receptors, G-Protein-Coupled / genetics
  • Receptors, G-Protein-Coupled / physiology*
  • Receptors, Neuropeptide / deficiency
  • Receptors, Neuropeptide / genetics
  • Receptors, Neuropeptide / physiology*

Substances

  • AstA-R1 protein, Drosophila
  • Drosophila Proteins
  • Kruppel-Like Transcription Factors
  • Receptors, G-Protein-Coupled
  • Receptors, Neuropeptide
  • Adenosine Triphosphatases
  • spas protein, Drosophila