Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

Exclusion of close linkage between the synaptic vesicular monoamine transporter locus and schizophrenia spectrum disorders

Journal Article · · American Journal of Medical Genetics
;  [1];  [2]
  1. Johns Hopkins Univ. School of Medicine, Baltimore, MD (United States)
  2. Universitario Campus Bio-Medico, Rome (Italy); and others

The principal brain synaptic vesicular monoamine transporter (VMAT2) is responsible for the reuptake of serotonin, dopamine, norepinephrine, epinephrine, and histamine from the cytoplasm into synaptic vesicles, thus contributing to determination of the size of releasable neurotransmitter vesicular pools. Potential involvement of VMAT2 gene variants in the etiology of schizophrenia and related disorders was tested using polymorphic VMAT2 gene markers in 156 subjects from 16 multiplex pedigrees with schizophrenia, schizophreniform, schizoaffective, and schizotypal disorders and mood incongruent psychotic depression. Assuming genetic homogeneity, complete ({theta} = 0.0) linkage to the schizophrenia spectrum was excluded under both dominant and recessive models. Allelic variants at the VMAT2 locus do not appear to provide major genetic contributions to the etiology of schizophrenia spectrum disorders in these pedigrees. 16 refs.

Sponsoring Organization:
USDOE
OSTI ID:
254412
Journal Information:
American Journal of Medical Genetics, Journal Name: American Journal of Medical Genetics Journal Issue: 6 Vol. 60; ISSN 0148-7299; ISSN AJMGDA
Country of Publication:
United States
Language:
English

Similar Records

Further association study on dopamine D2 receptor variant S311C in Schizophrenia and affective disorders
Journal Article · Tue Apr 09 00:00:00 EDT 1996 · American Journal of Medical Genetics · OSTI ID:447655

Structural mechanisms for VMAT2 inhibition by tetrabenazine
Journal Article · Fri Mar 22 00:00:00 EDT 2024 · eLife · OSTI ID:2471655

Search for a schizophrenia susceptibility locus of human chromosome 22
Journal Article · Wed Jun 15 00:00:00 EDT 1994 · American Journal of Medical Genetics · OSTI ID:91089