Exclusion of close linkage of bipolar disorder to the dopamine D3 receptor gene in nine Australian pedigrees

Philip Mitchell*, Brent Waters, Christina Vivero, Fie Le, Jennifer Donald, Michele Tully, Karen Campedelli, Lars Lannfelt, Pierre Sokoloff, John Shine, Lisa Selbie

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

17 Citations (Scopus)

Abstract

The recently cloned dopamine D3 receptor (DRD3) gene is of potential relevance to the aetiology of bipolar disorder because of an almost exclusive expression in limbic tissue, the region of the brain putatively responsible for control of emotion. We therefore aimed to determine whether bipolar disorder in nine pedigrees (with 171 members) was linked to this receptor gene, which has been mapped to chromosomal region 3q 13.3. Linkage of bipolar disorder and recurrent depression to the DRD3 gene was tested using a series of autosomal dominant and recessive models with varying penetrance levels. Additionally, linkage was examined using a series of levels of definitions of affective illness (ranging from bipolar I alone to all affective disorders). Close linkage to the DRD3 gene was strongly excluded using each model and definition, and these conclusions persisted when a wide range of rates of 'sporadic' (non-genetic) presentations of illness were incorporated in the analysis.

Original languageEnglish
Pages (from-to)213-224
Number of pages12
JournalJournal of Affective Disorders
Volume27
Issue number4
DOIs
Publication statusPublished - 1993

Keywords

  • Bipolar disorder
  • Chromosome 3
  • Dopamine D receptor
  • Linkage

Fingerprint

Dive into the research topics of 'Exclusion of close linkage of bipolar disorder to the dopamine D<sub>3</sub> receptor gene in nine Australian pedigrees'. Together they form a unique fingerprint.

Cite this