Drosophila Naked cuticle (Nkd) engages the nuclear import adaptor Importin-alpha3 to antagonize Wnt/beta-catenin signaling

Dev Biol. 2008 Jun 1;318(1):17-28. doi: 10.1016/j.ydbio.2008.02.050. Epub 2008 Mar 18.

Abstract

Precise control of Wnt/beta-catenin signaling is critical for animal development, stem cell renewal, and prevention of disease. In the fruit fly Drosophila melanogaster, the naked cuticle (nkd) gene limits signaling by the Wnt ligand Wingless (Wg) during embryo segmentation. Nkd is an intracellular protein that is composed of separable membrane- and nuclear-localization sequences (NLS) as well as a conserved EF-hand motif that binds the Wnt receptor-associated scaffold protein Dishevelled (Dsh), but the mechanism by which Nkd inhibits Wnt signaling remains a mystery. Here we identify a second NLS in Nkd that is required for full activity and that binds to the canonical nuclear import adaptor Importin-alpha3. The Nkd NLS is similar to the Importin-alpha3-binding NLS in the Drosophila heat-shock transcription factor (dHSF), and each Importin-alpha3-binding NLS required intact basic residues in similar positions for nuclear import and protein function. Our results provide further support for the hypothesis that Nkd inhibits nuclear step(s) in Wnt/beta-catenin signaling and broaden our understanding of signaling pathways that engage the nuclear import machinery.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Active Transport, Cell Nucleus / physiology
  • Adaptor Proteins, Signal Transducing / genetics
  • Adaptor Proteins, Signal Transducing / metabolism
  • Amino Acid Sequence
  • Animals
  • Dishevelled Proteins
  • Drosophila Proteins / genetics
  • Drosophila Proteins / metabolism*
  • Drosophila melanogaster* / anatomy & histology
  • Drosophila melanogaster* / embryology
  • Drosophila melanogaster* / genetics
  • Drosophila melanogaster* / metabolism
  • Female
  • Molecular Sequence Data
  • Nuclear Localization Signals
  • Phosphoproteins / genetics
  • Phosphoproteins / metabolism
  • RNA Interference
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • Salivary Glands / cytology
  • Salivary Glands / embryology
  • Salivary Glands / metabolism
  • Sequence Alignment
  • Signal Transduction / physiology*
  • Two-Hybrid System Techniques
  • Wnt Proteins / genetics
  • Wnt Proteins / metabolism*
  • alpha Karyopherins / genetics
  • alpha Karyopherins / metabolism*
  • beta Catenin / genetics
  • beta Catenin / metabolism*

Substances

  • Adaptor Proteins, Signal Transducing
  • Dishevelled Proteins
  • Drosophila Proteins
  • Kap-alpha3 protein, Drosophila
  • Nuclear Localization Signals
  • Phosphoproteins
  • Recombinant Fusion Proteins
  • Wnt Proteins
  • alpha Karyopherins
  • beta Catenin
  • dsh protein, Drosophila
  • nkd protein, Drosophila