Hindsight regulates photoreceptor axon targeting through transcriptional control of jitterbug/Filamin and multiple genes involved in axon guidance in Drosophila

Dev Neurobiol. 2015 Sep;75(9):1018-32. doi: 10.1002/dneu.22271. Epub 2015 Feb 18.

Abstract

During axon targeting, a stereotyped pattern of connectivity is achieved by the integration of intrinsic genetic programs and the response to extrinsic long and short-range directional cues. How this coordination occurs is the subject of intense study. Transcription factors play a central role due to their ability to regulate the expression of multiple genes required to sense and respond to these cues during development. Here we show that the transcription factor HNT regulates layer-specific photoreceptor axon targeting in Drosophila through transcriptional control of jbug/Filamin and multiple genes involved in axon guidance and cytoskeleton organization.Using a microarray analysis we identified 235 genes whose expression levels were changed by HNT overexpression in the eye primordia. We analyzed nine candidate genes involved in cytoskeleton regulation and axon guidance, six of which displayed significantly altered gene expression levels in hnt mutant retinas. Functional analysis confirmed the role of OTK/PTK7 in photoreceptor axon targeting and uncovered Tiggrin, an integrin ligand, and Jbug/Filamin, a conserved actin- binding protein, as new factors that participate of photoreceptor axon targeting. Moreover, we provided in silico and molecular evidence that supports jbug/Filamin as a direct transcriptional target of HNT and that HNT acts partially through Jbug/Filamin in vivo to regulate axon guidance. Our work broadens the understanding of how HNT regulates the coordinated expression of a group of genes to achieve the correct connectivity pattern in the Drosophila visual system. © 2015 Wiley Periodicals, Inc. Develop Neurobiol 75: 1018-1032, 2015.

Keywords: Drosophila; Filamins; axon targeting; hindsight.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Genetically Modified
  • Axons / physiology*
  • Cell Line
  • Cell Movement / physiology*
  • Cytoskeleton / metabolism
  • Drosophila
  • Drosophila Proteins / metabolism*
  • Extracellular Matrix Proteins / metabolism
  • Filamins / metabolism*
  • Nuclear Proteins / metabolism*
  • Photoreceptor Cells, Invertebrate / physiology*
  • Receptor Protein-Tyrosine Kinases / metabolism
  • Retina / growth & development
  • Retina / physiology
  • Transcription Factors / metabolism*

Substances

  • Drosophila Proteins
  • Extracellular Matrix Proteins
  • Filamins
  • Nuclear Proteins
  • Tig protein, Drosophila
  • Transcription Factors
  • peb protein, Drosophila
  • Otk protein, Drosophila
  • Receptor Protein-Tyrosine Kinases