Systematic screening for mutations in the glycine receptor alpha2 subunit gene (GLRA2) in patients with schizophrenia and other psychiatric diseases.

Abstract

The glycine receptor, which is a member of the ligand-gated ion channel superfamily, mediates synaptic inhibition in the spinal cord and other brain regions. This superfamily has been implicated in the pathogenesis of schizophrenia and other psychiatric diseases. The complete coding sequence and splice junctions of the GLRA2 gene were scanned by DOVAM-S, a form of SSCP analysis with sufficient redundancy to detect virtually all mutations. Those analyses were performed in 113 patients with schizophrenia, and in pilot studies of patients with bipolar illness, alcoholism, puerperal psychosis, autism, and attention-deficit hyperactivity disorder (533 kb total scanned sequences). We detected three sequence changes in the coding region, all resulting in silent mutations: C894T in exon 5, C1134T in exon 7, and C1476T in exon 9. These do not alter the structure or the expression of the protein. It is unlikely that mutations in the coding region and splice junction of GLRA2 gene are associated with schizophrenia and other psychiatric diseases.

• Authors: J Feng, N Craddock, I R Jones, E H Cook Jr, D Goldman, L L Heston, L Peltonen, L E DeLisi, S S Sommer
• Journal: Psychiatric genetics (Psychiatr Genet) Vol. 11 Issue 1 Pg. 45-8 (Mar 2001) ISSN: 0955-8829 [Print] England
• PMID: 11409700 (Publication Type: Journal Article)

Chemical References

• DNA Primers
• GLRA2 protein, human
• Protein Subunits
• Receptors, Glycine

Topics

• Alcoholism (genetics)
• Alternative Splicing (genetics)
• Attention Deficit Disorder with Hyperactivity (genetics)
• Base Sequence
• DNA Primers
• Exons
• Female
• Humans
• Mutation
• Pilot Projects
• Polymerase Chain Reaction
• Pregnancy
• Protein Subunits
• Psychotic Disorders (genetics)
• Puerperal Disorders (genetics)
• Receptors, Glycine (genetics)
• Schizophrenia (genetics)