Regulation of effectors by G-protein alpha- and beta gamma-subunits. Recent insights from studies of the phospholipase c-beta isoenzymes

Biochem Pharmacol. 1997 Aug 15;54(4):429-35. doi: 10.1016/s0006-2952(97)00032-4.

Abstract

Both the alpha- and beta gamma-subunits of heterotrimeric guanine nucleotide-dependent regulatory proteins (G-proteins) couple members of the heptahelical class of cell-surface receptors to a diverse range of signal-generating effectors including retinal cyclic GMP phosphodiesterase, ion channels, adenylylcyclases, phosphoinositide 3-kinase, and members of the beta-class of inositol lipid-specific phospholipases C. Although the molecular details of the G-protein-regulated phospholipase C system were elucidated comparatively recently, these enzymes have become an important model for investigations of the process of G-protein effector coupling. A combination of molecular biological, biochemical, and structural studies using the phospholipase C-beta enzymes has provided some important insights into the interplay between G-proteins and their effectors and promises to reveal the mechanisms by which G-protein alpha- and beta gamma-subunits selectively associate with and activate effectors.

Publication types

  • Review

MeSH terms

  • Animals
  • Enzyme Activation
  • GTP-Binding Proteins / physiology*
  • Humans
  • Isoenzymes / metabolism*
  • Type C Phospholipases / metabolism*

Substances

  • Isoenzymes
  • Type C Phospholipases
  • GTP-Binding Proteins