The protein arginine methyltransferase PRMT5 promotes D2-like dopamine receptor signaling

Sci Signal. 2015 Nov 10;8(402):ra115. doi: 10.1126/scisignal.aad0872.

Abstract

Protein arginine methylation regulates diverse functions of eukaryotic cells, including gene expression, the DNA damage response, and circadian rhythms. We showed that arginine residues within the third intracellular loop of the human D2 dopamine receptor, which are conserved in the DOP-3 receptor in the nematode Caenorhabditis elegans, were methylated by protein arginine methyltransferase 5 (PRMT5). By mutating these arginine residues, we further showed that their methylation enhanced the D2 receptor-mediated inhibition of cyclic adenosine monophosphate (cAMP) signaling in cultured human embryonic kidney (HEK) 293T cells. Analysis of prmt-5-deficient worms indicated that methylation promoted the dopamine-mediated modulation of chemosensory and locomotory behaviors in C. elegans through the DOP-3 receptor. In addition to delineating a previously uncharacterized means of regulating GPCR (heterotrimeric guanine nucleotide-binding protein-coupled receptor) signaling, these findings may lead to the development of a new class of pharmacological therapies that modulate GPCR signaling by changing the methylation status of these key proteins.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Amino Acid Motifs
  • Amino Acid Sequence
  • Animals
  • Animals, Genetically Modified
  • Arginine / chemistry
  • Caenorhabditis elegans / drug effects
  • Caenorhabditis elegans / genetics
  • Caenorhabditis elegans / metabolism
  • Caenorhabditis elegans Proteins / chemistry
  • Caenorhabditis elegans Proteins / genetics
  • Caenorhabditis elegans Proteins / metabolism
  • Computational Biology
  • Conserved Sequence
  • Dopamine / metabolism
  • Dopamine / pharmacology
  • HEK293 Cells
  • Humans
  • Locomotion / drug effects
  • Locomotion / genetics
  • Locomotion / physiology
  • Methylation
  • Molecular Sequence Data
  • Octanols / pharmacology
  • Odorants
  • Protein-Arginine N-Methyltransferases / deficiency
  • Protein-Arginine N-Methyltransferases / genetics
  • Protein-Arginine N-Methyltransferases / metabolism*
  • Receptors, Dopamine D2 / chemistry
  • Receptors, Dopamine D2 / genetics
  • Receptors, Dopamine D2 / metabolism*
  • Receptors, G-Protein-Coupled / chemistry
  • Receptors, G-Protein-Coupled / genetics
  • Receptors, G-Protein-Coupled / metabolism
  • Sequence Homology, Amino Acid
  • Signal Transduction

Substances

  • Caenorhabditis elegans Proteins
  • DOP-3 protein, C elegans
  • DRD2 protein, human
  • Octanols
  • Receptors, Dopamine D2
  • Receptors, G-Protein-Coupled
  • Arginine
  • PRMT5 protein, human
  • Protein-Arginine N-Methyltransferases
  • prmt-5 protein, C elegans
  • Dopamine