In Vivo Interaction Proteomics in Caenorhabditis elegans Embryos Provides New Insights into P Granule Dynamics

Mol Cell Proteomics. 2016 May;15(5):1642-57. doi: 10.1074/mcp.M115.053975. Epub 2016 Feb 24.

Abstract

Studying protein interactions in whole organisms is fundamental to understanding development. Here, we combine in vivo expressed GFP-tagged proteins with quantitative proteomics to identify protein-protein interactions of selected key proteins involved in early C. elegans embryogenesis. Co-affinity purification of interaction partners for eight bait proteins resulted in a pilot in vivo interaction map of proteins with a focus on early development. Our network reflects known biology and is highly enriched in functionally relevant interactions. To demonstrate the utility of the map, we looked for new regulators of P granule dynamics and found that GEI-12, a novel binding partner of the DYRK family kinase MBK-2, is a key regulator of P granule formation and germline maintenance. Our data corroborate a recently proposed model in which the phosphorylation state of GEI-12 controls P granule dynamics. In addition, we find that GEI-12 also induces granule formation in mammalian cells, suggesting a common regulatory mechanism in worms and humans. Our results show that in vivo interaction proteomics provides unique insights into animal development.

MeSH terms

  • Animals
  • Caenorhabditis elegans / embryology*
  • Caenorhabditis elegans / metabolism
  • Caenorhabditis elegans Proteins / analysis*
  • Caenorhabditis elegans Proteins / metabolism
  • Carrier Proteins / metabolism*
  • Chromatography, Affinity
  • Cytoplasmic Granules / metabolism
  • Dyrk Kinases
  • Gene Expression Regulation, Developmental
  • Mass Spectrometry
  • Phosphorylation
  • Protein Interaction Maps
  • Protein Serine-Threonine Kinases / metabolism*
  • Protein-Tyrosine Kinases / metabolism*
  • Proteomics / methods*

Substances

  • Caenorhabditis elegans Proteins
  • Carrier Proteins
  • GEI-12 protein, C elegans
  • MBK-2 protein, C elegans
  • Protein-Tyrosine Kinases
  • Protein Serine-Threonine Kinases