Phosphorylation of critical serine residues in Gem separates cytoskeletal reorganization from down-regulation of calcium channel activity

Mol Cell Biol. 2004 Jan;24(2):651-61. doi: 10.1128/MCB.24.2.651-661.2004.

Abstract

Gem is a small GTP-binding protein that has a ras-like core and extended chains at each terminus. The primary structure of Gem and other RGK family members (Rad, Rem, and Rem2) predicts a GTPase deficiency, leading to the question of how Gem functional activity is regulated. Two functions for Gem have been demonstrated, including inhibition of voltage-gated calcium channel activity and inhibition of Rho kinase-mediated cytoskeletal reorganization, such as stress fiber formation and neurite retraction. These functions for Gem have been ascribed to its interaction with the calcium channel beta subunit and Rho kinase beta, respectively. We show here that these functions are separable and regulated by distinct structural modifications to Gem. Phosphorylation of serines 261 and 289, located in the C-terminal extension, is required for Gem-mediated cytoskeletal reorganization, while GTP and possibly calmodulin binding are required for calcium channel inhibition. In addition to regulating cytoskeletal reorganization, phosphorylation of serine 289 in conjunction with serine 23 results in bidentate 14-3-3 binding, leading to increased Gem protein half-life. Evidence presented shows that phosphorylation of serine 261 is mediated via a cdc42/protein kinase Czeta-dependent pathway. These data demonstrate that phosphorylation of serines 261 and 289, outside the GTP-binding region of Gem, controls its inhibition of Rho kinase beta and associated changes in the cytoskeleton.

MeSH terms

  • 14-3-3 Proteins
  • Animals
  • Binding Sites / genetics
  • COS Cells
  • Calcium Channels / metabolism*
  • Cytoskeleton / metabolism
  • Down-Regulation
  • Half-Life
  • Humans
  • Immediate-Early Proteins / chemistry*
  • Immediate-Early Proteins / genetics
  • Immediate-Early Proteins / metabolism*
  • In Vitro Techniques
  • Mice
  • Monomeric GTP-Binding Proteins / chemistry*
  • Monomeric GTP-Binding Proteins / genetics
  • Monomeric GTP-Binding Proteins / metabolism*
  • Neurites / metabolism
  • Neurites / ultrastructure
  • Phosphorylation
  • Protein Kinase C / metabolism
  • Rats
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Serine / chemistry
  • Transfection
  • Two-Hybrid System Techniques
  • Tyrosine 3-Monooxygenase / metabolism

Substances

  • 14-3-3 Proteins
  • Calcium Channels
  • Immediate-Early Proteins
  • Recombinant Proteins
  • Serine
  • Tyrosine 3-Monooxygenase
  • protein kinase C zeta
  • Protein Kinase C
  • GEM protein, human
  • Gem protein, mouse
  • Monomeric GTP-Binding Proteins