Nemo phosphorylates Eyes absent and enhances output from the Eya-Sine oculis transcriptional complex during Drosophila retinal determination

Dev Biol. 2012 May 1;365(1):267-76. doi: 10.1016/j.ydbio.2012.02.030. Epub 2012 Feb 25.

Abstract

The retinal determination gene network comprises a collection of transcription factors that respond to multiple signaling inputs to direct Drosophila eye development. Previous genetic studies have shown that nemo (nmo), a gene encoding a proline-directed serine/threonine kinase, can promote retinal specification through interactions with the retinal determination gene network, although the molecular point of cross-talk was not defined. Here, we report that the Nemo kinase positively and directly regulates Eyes absent (Eya). Genetic assays show that Nmo catalytic activity enhances Eya-mediated ectopic eye formation and potentiates induction of the Eya-Sine oculis (So) transcriptional targets dachshund and lozenge. Biochemical analyses demonstrate that Nmo forms a complex with and phosphorylates Eya at two consensus mitogen-activated protein kinase (MAPK) phosphorylation sites. These same sites appear crucial for Nmo-mediated activation of Eya function in vivo. Thus, we propose that Nmo phosphorylation of Eya potentiates its transactivation function to enhance transcription of Eya-So target genes during eye specification and development.

Publication types

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

MeSH terms

  • Animals
  • Drosophila / embryology*
  • Drosophila Proteins / physiology*
  • Eye / embryology*
  • Eye Proteins / physiology*
  • Homeodomain Proteins / physiology*
  • Mitogen-Activated Protein Kinases / physiology*
  • Organogenesis
  • Phosphorylation
  • Retina / embryology
  • Retina / physiology
  • Transcriptional Activation

Substances

  • Drosophila Proteins
  • Eye Proteins
  • Homeodomain Proteins
  • So protein, Drosophila
  • eya protein, Drosophila
  • Mitogen-Activated Protein Kinases
  • nmo protein, Drosophila