The SH2-SH2-SH3 domain of phospholipase C-gamma1 directly binds to translational elongation factor-1alpha

Mol Cells. 1999 Dec 31;9(6):631-7.

Abstract

Phospholipase C-gamma1 (PLC-gamma1) is a lipase that hydrolyzes PIP2 to generate two second messengers, IP3 and DAG. By using the yeast two-hybrid system, we identified the translational elongation factor-1alpha (EF-1alpha) as a binding protein of PLC-gamma1 from the human B-lymphocyte library. Direct interaction between EF-1alpha and PLC-gamma1 was confirmed by the in vitro binding experiment using purified PLC-gamma1. Furthermore, from the in vitro binding experiment, we could demonstrate that the carboxyl terminal region of EF-1alpha is involved in the interaction with PLC-gamma1, and that both SH2 and SH3 domains of PLC-gamma1 are required for the interaction with EF-1alpha. In vivo interaction between EF-1alpha and PLC-gamma1 was confirmed by the immunoprecipitation experiment using anti-EF-1alpha antibody. The interaction between EF-1alpha and PLC-gamma1 was enhanced by EGF-treatment. Taken together, we suggest that EF-1alpha might play a role in PLC-gamma1-mediated signal transduction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • COS Cells
  • Humans
  • Isoenzymes / metabolism*
  • Lymphocytes / metabolism
  • Peptide Elongation Factor 1 / metabolism*
  • Phospholipase C gamma
  • Precipitin Tests
  • Protein Binding
  • Signal Transduction
  • Transfection
  • Type C Phospholipases / metabolism*
  • Yeasts
  • src Homology Domains*

Substances

  • Isoenzymes
  • Peptide Elongation Factor 1
  • Type C Phospholipases
  • Phospholipase C gamma