Regulation of G-protein coupled receptor traffic by an evolutionary conserved hydrophobic signal

Traffic. 2010 Apr;11(4):560-78. doi: 10.1111/j.1600-0854.2010.01033.x. Epub 2010 Jan 6.

Abstract

Plasma membrane (PM) expression of G-protein coupled receptors (GPCRs) is required for activation by extracellular ligands; however, mechanisms that regulate PM expression of GPCRs are poorly understood. For some GPCRs, such as alpha2c-adrenergic receptors (alpha(2c)-ARs), heterologous expression in non-native cells results in limited PM expression and extensive endoplasmic reticulum (ER) retention. Recently, ER export/retentions signals have been proposed to regulate cellular trafficking of several GPCRs. By utilizing a chimeric alpha(2a)/alpha(2c)-AR strategy, we identified an evolutionary conserved hydrophobic sequence (ALAAALAAAAA) in the extracellular amino terminal region that is responsible in part for alpha(2c)-AR subtype-specific trafficking. To our knowledge, this is the first luminal ER retention signal reported for a GPCR. Removal or disruption of the ER retention signal dramatically increased PM expression and decreased ER retention. Conversely, transplantation of this hydrophobic sequence into alpha(2a)-ARs reduced their PM expression and increased ER retention. This evolutionary conserved hydrophobic trafficking signal within alpha(2c)-ARs serves as a regulator of GPCR trafficking.

Keywords: ER export; ER retention; GPCR trafficking; protein sorting; retention signal.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Conserved Sequence*
  • Endoplasmic Reticulum / metabolism
  • Evolution, Molecular
  • Hydrophobic and Hydrophilic Interactions
  • PC12 Cells
  • Protein Sorting Signals*
  • Protein Transport
  • Rats
  • Receptors, Adrenergic, alpha-2 / genetics
  • Receptors, Adrenergic, alpha-2 / metabolism
  • Receptors, G-Protein-Coupled / genetics
  • Receptors, G-Protein-Coupled / metabolism*
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • Signal Transduction / physiology

Substances

  • Protein Sorting Signals
  • Receptors, Adrenergic, alpha-2
  • Receptors, G-Protein-Coupled
  • Recombinant Fusion Proteins