Intracellular trafficking of guanylate-binding proteins is regulated by heterodimerization in a hierarchical manner

PLoS One. 2010 Dec 7;5(12):e14246. doi: 10.1371/journal.pone.0014246.

Abstract

Guanylate-binding proteins (GBPs) belong to the dynamin family of large GTPases and represent the major IFN-γ-induced proteins. Here we systematically investigated the mechanisms regulating the subcellular localization of GBPs. Three GBPs (GBP-1, GBP-2 and GBP-5) carry a C-terminal CaaX-prenylation signal, which is typical for small GTPases of the Ras family, and increases the membrane affinity of proteins. In this study, we demonstrated that GBP-1, GBP-2 and GBP-5 are prenylated in vivo and that prenylation is required for the membrane association of GBP-1, GBP-2 and GBP-5. Using co-immunoprecipitation, yeast-two-hybrid analysis and fluorescence complementation assays, we showed for the first time that GBPs are able to homodimerize in vivo and that the membrane association of GBPs is regulated by dimerization similarly to dynamin. Interestingly, GBPs could also heterodimerize. This resulted in hierarchical positioning effects on the intracellular localization of the proteins. Specifically, GBP-1 recruited GBP-5 and GBP-2 into its own cellular compartment and GBP-5 repositioned GBP-2. In addition, GBP-1, GBP-2 and GBP-5 were able to redirect non-prenylated GBPs to their compartment in a prenylation-dependent manner. Overall, these findings prove in vivo the ability of GBPs to dimerize, indicate that heterodimerization regulates sub-cellular localization of GBPs and underscore putative membrane-associated functions of this family of proteins.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Motifs
  • Cell Proliferation
  • Dimerization
  • Flow Cytometry
  • GTP Phosphohydrolases / chemistry
  • GTP-Binding Proteins / metabolism*
  • Golgi Apparatus / metabolism
  • HeLa Cells
  • Humans
  • Microscopy, Fluorescence
  • Models, Biological
  • Mutation
  • Protein Transport
  • Subcellular Fractions
  • Two-Hybrid System Techniques

Substances

  • GTP Phosphohydrolases
  • GTP-Binding Proteins