Serine racemase is associated with schizophrenia susceptibility in humans and in a mouse model

Hum Mol Genet. 2009 Sep 1;18(17):3227-43. doi: 10.1093/hmg/ddp261. Epub 2009 May 30.

Abstract

Abnormal N-methyl-d-aspartate receptor (NMDAR) function has been implicated in the pathophysiology of schizophrenia. d-serine is an important NMDAR modulator, and to elucidate the role of the d-serine synthesis enzyme serine racemase (Srr) in schizophrenia, we identified and characterized mice with an ENU-induced mutation that results in a complete loss of Srr activity and dramatically reduced d-serine levels. Mutant mice displayed behaviors relevant to schizophrenia, including impairments in prepulse inhibition, sociability and spatial discrimination. Behavioral deficits were exacerbated by an NMDAR antagonist and ameliorated by d-serine or the atypical antipsychotic clozapine. Expression profiling revealed that the Srr mutation influenced several genes that have been linked to schizophrenia and cognitive ability. Transcript levels altered by the Srr mutation were also normalized by d-serine or clozapine treatment. Furthermore, analysis of SRR genetic variants in humans identified a robust association with schizophrenia. This study demonstrates that aberrant Srr function and diminished d-serine may contribute to schizophrenia pathogenesis.

Publication types

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

MeSH terms

  • Animals
  • Case-Control Studies
  • Disease Models, Animal
  • Disease Susceptibility*
  • Female
  • Humans
  • Male
  • Mice
  • Mice, Inbred Strains
  • Mutation
  • Pedigree
  • Racemases and Epimerases / genetics
  • Racemases and Epimerases / metabolism*
  • Schizophrenia / enzymology*
  • Schizophrenia / genetics
  • Schizophrenia / physiopathology
  • Serine / metabolism

Substances

  • Serine
  • Racemases and Epimerases
  • serine racemase