Identification of a missense mutation and several polymorphisms in the proenkephalin A gene of schizophrenic patients

Am J Med Genet. 1996 Sep 20;67(5):459-67. doi: 10.1002/(SICI)1096-8628(19960920)67:5<459::AID-AJMG4>3.0.CO;2-F.

Abstract

Schizophrenia is a complex and severe disorder of unknown cause and pathophysiology. In this study, we examined the opioid hypothesis for schizophrenia at the molecular level, focusing on the dopamine-regulated proenkephalin A gene (chromosome 8q11.23-q12). We have screened 150 schizophrenic patients for sequence variations within the promoter region, entire coding sequence, and 3'-untranslated region. We find one sequence change in a conserved amino acid that may be of functional significance. This mutation was found in a single schizophrenia patient but not in controls. Although several new, race-specific polymorphisms were identified, all other sequence changes appeared to be common polymorphisms, unlikely to contribute to the etiology of schizophrenia.

Publication types

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

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • Chromosome Mapping
  • Chromosomes, Human, Pair 8*
  • Codon
  • Conserved Sequence
  • Enkephalins / genetics*
  • Exons
  • Genetic Variation
  • Humans
  • Point Mutation*
  • Polymorphism, Genetic*
  • Promoter Regions, Genetic
  • Protein Precursors / genetics*
  • Schizophrenia / genetics*

Substances

  • Codon
  • Enkephalins
  • Protein Precursors
  • proenkephalin