GIV/Girdin transmits signals from multiple receptors by triggering trimeric G protein activation

J Biol Chem. 2015 Mar 13;290(11):6697-704. doi: 10.1074/jbc.R114.613414. Epub 2015 Jan 20.

Abstract

Activation of trimeric G proteins has been traditionally viewed as the exclusive job of G protein-coupled receptors (GPCRs). This view has been challenged by the discovery of non-receptor activators of trimeric G proteins. Among them, GIV (a.k.a. Girdin) is the first for which a guanine nucleotide exchange factor (GEF) activity has been unequivocally associated with a well defined motif. Here we discuss how GIV assembles alternative signaling pathways by sensing cues from various classes of surface receptors and relaying them via G protein activation. We also describe the dysregulation of this mechanism in disease and how its targeting holds promise for novel therapeutics.

Keywords: Guanine Nucleotide Exchange Factor (GEF); Heterotrimeric G Protein; Liver Fibrosis; Nephrotic Syndrome; Receptor Tyrosine Kinase; Src Homology 2 Domain (SH2 Domain); Tumor Metastasis.

Publication types

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

MeSH terms

  • Animals
  • Cell Movement
  • Cell Survival
  • GTP-Binding Proteins / chemistry
  • GTP-Binding Proteins / metabolism*
  • Humans
  • Liver Cirrhosis / metabolism
  • Microfilament Proteins / chemistry
  • Microfilament Proteins / metabolism*
  • Mitosis
  • Models, Molecular
  • Neoplasm Metastasis / pathology
  • Neoplasms / metabolism
  • Neoplasms / pathology
  • Nephrotic Syndrome / metabolism
  • Protein Multimerization
  • Receptors, Cell Surface / metabolism*
  • Signal Transduction*
  • Vesicular Transport Proteins / chemistry
  • Vesicular Transport Proteins / metabolism*

Substances

  • CCDC88A protein, human
  • Microfilament Proteins
  • Receptors, Cell Surface
  • Vesicular Transport Proteins
  • GTP-Binding Proteins