Interaction of elongation factor-1alpha and pleckstrin homology domain of phospholipase C-gamma 1 with activating its activity

J Biol Chem. 2002 May 31;277(22):19697-702. doi: 10.1074/jbc.M111206200. Epub 2002 Mar 8.

Abstract

The pleckstrin homology (PH) domain is a small motif for membrane targeting in the signaling molecules. Phospholipase C (PLC)-gamma1 has two putative PH domains, an NH(2)-terminal and a split PH domain. Here we report studies on the interaction of the PH domain of PLC-gamma1 with translational elongation factor (EF)-1alpha, which has been shown to be a phosphatidylinositol 4-kinase activator. By pull-down of cell extract with the glutathione S-transferase (GST) fusion proteins with various domains of PLC-gamma1 followed by peptide sequence analysis, we identified EF-1alpha as a binding partner of a split PH domain of PLC-gamma1. Analysis by site-directed mutagenesis of the PH domain revealed that the beta2-sheet of a split PH domain is critical for the interaction with EF-1alpha. Moreover, Dot-blot assay shows that a split PH domain specifically binds to phosphoinositides including phosphatidylinositol 4-phosphate and phosphatidylinositol 4, 5-bisphosphate (PIP(2)). So the PH domain of PLC-gamma1 binds to both EF-1alpha and PIP(2). The binding affinity of EF-1alpha to the GST.PH domain fusion protein increased in the presence of PIP(2), although PIP(2) does not bind to EF-1alpha directly. This suggests that EF-1alpha may control the binding affinity between the PH domain and PIP(2). PLC-gamma1 is substantially activated in the presence of EF-1alpha with a bell-shaped curve in relation to the molar ratio between them, whereas a double point mutant PLC-gamma1 (Y509A/F510A) that lost its binding affinity to EF-1alpha shows basal level activity. Taken together, our data show that EF-1alpha plays a direct role in phosphoinositide metabolism of cellular signaling by regulating PLC-gamma1 activity via a split PH domain.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 1-Phosphatidylinositol 4-Kinase / metabolism
  • 3T3 Cells
  • Amino Acid Sequence
  • Animals
  • Binding Sites
  • Blood Proteins / chemistry*
  • Blotting, Western
  • Glutathione Transferase / metabolism
  • Humans
  • Isoenzymes / metabolism*
  • Mice
  • Molecular Sequence Data
  • Mutagenesis, Site-Directed
  • Peptide Elongation Factor 1 / chemistry*
  • Peptide Elongation Factor 1 / metabolism*
  • Peptides / chemistry
  • Phospholipase C gamma
  • Phospholipids / chemistry
  • Phosphoproteins / chemistry*
  • Point Mutation
  • Protein Binding
  • Protein Biosynthesis
  • Protein Structure, Secondary
  • Protein Structure, Tertiary
  • Rats
  • Recombinant Fusion Proteins / metabolism
  • Sequence Homology, Amino Acid
  • Signal Transduction
  • Type C Phospholipases / metabolism*

Substances

  • Blood Proteins
  • Isoenzymes
  • Peptide Elongation Factor 1
  • Peptides
  • Phospholipids
  • Phosphoproteins
  • Recombinant Fusion Proteins
  • platelet protein P47
  • Glutathione Transferase
  • 1-Phosphatidylinositol 4-Kinase
  • Type C Phospholipases
  • Phospholipase C gamma