Transgenic rescue for characterizing orphan receptors: a review of delta2 glutamate receptor

Transgenic Res. 2005 Apr;14(2):117-21. doi: 10.1007/s11248-005-2685-6.

Abstract

Even though the genomes of several major species have been sequenced, many orphan receptors with unknown ligands and mechanisms of action remain in the CNS. The delta2 glutamate receptor (GluRdelta2) is one of such receptors expressed predominantly in the cerebellar Purkinje cells. On the basis of amino acid similarity, it belongs to ionotropic glutamate receptor (iGluR) family, which mediates fast excitatory neurotransmission in the mammalian CNS. Although its null-mutant mice show prominent motor discoordination, the mechanisms by which GluRdelta2 participates in the cerebellar functions have been unclear. To gain insight into GluRdelta2's mechanisms, we recently generated mice that express either a wild-type or a mutant GIuRdelta2 transgene, in which the conserved arginine in GluRdelta2's N-terminal putative ligand-binding motif was disrupted. By breeding these transgenic mice onto a GluRdelta2 -/- background, we obtained two transgenic 'rescue' lines. Surprisingly, the mutant GluRdelta2 transgene was as effective as the wild-type GluRdelta2 in rescuing the GluRdelta2-null mice. As the disrupted arginine residue is highly conserved from ancestral bacterial periplasmic amino acid-binding proteins to mammalian iGluRs, we propose that GIuRdelta2 may not require glutamate-like amino acids and may function in an unconventional manner. This 'transgenic rescue' approach to investigating orphan receptors is a relatively easy but powerful method when a knockout mouse with a distinct phenotype is already available. The advantages and limitations of this approach, together with certain cautions in interpreting the resulting data, are discussed in this review.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Breeding
  • Cerebellum / physiology*
  • Female
  • Male
  • Mice
  • Mice, Knockout
  • Mutation
  • Phenotype
  • Receptors, Glutamate / genetics*
  • Receptors, Glutamate / physiology*
  • Transgenes*

Substances

  • Receptors, Glutamate
  • glutamate receptor delta 2