Dopamine receptor D4

The dopamine receptor D4 is a dopamine D2-like G protein-coupled receptor encoded by the DRD4 gene on chromosome 11 at 11p15.5.[5]

DRD4
Identifiers
AliasesDRD4, D4DR, dopamine receptor D4
External IDsOMIM: 126452 MGI: 94926 HomoloGene: 20215 GeneCards: DRD4
Gene location (Human)
Chr.Chromosome 11 (human)[1]
Band11p15.5Start637,269 bp[1]
End640,706 bp[1]
RNA expression pattern
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez

1815

13491

Ensembl

ENSG00000069696
ENSG00000276825

ENSMUSG00000025496

UniProt

P21917

P51436

RefSeq (mRNA)

NM_000797

NM_007878

RefSeq (protein)

NP_000788

NP_031904

Location (UCSC)Chr 11: 0.64 – 0.64 MbChr 7: 141.29 – 141.3 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

The structure of DRD4 was recently reported in complex with the antipsychotic drug nemonapride.[6]

As with other dopamine receptor subtypes, the D4 receptor is activated by the neurotransmitter dopamine. It is linked to many neurological and psychiatric conditions[7] including schizophrenia and bipolar disorder,[8] ADHD,[9][10] addictive behaviors,[11] Parkinson's disease,[12] and eating disorders such as anorexia nervosa.[13] A weak association has been drawn between DRD4 and borderline personality disorder.

It is also a target for drugs which treat schizophrenia and Parkinson's disease.[14] The D4 receptor is considered to be D2-like in which the activated receptor inhibits the enzyme adenylate cyclase, thereby reducing the intracellular concentration of the second messenger cyclic AMP.[15]

Genetics

The human protein is coded by the DRD4 on chromosome 11 located in 11p15.5.[16]

There are slight variations (mutations/polymorphisms) in the human gene:

  • A 48-base pair VNTR in exon 3
  • C-521T in the promoter
  • 13-base pair deletion of bases 235 to 247 in exon 1
  • 12 base pair repeat in exon 1[17]
  • Val194Gly
  • A polymorphic tandem duplication of 48 bp[18]

Mutations in this gene have been associated with various behavioral phenotypes, including autonomic nervous system dysfunction, attention deficit/hyperactivity disorder,[19] schizophrenia[20] and the personality trait of novelty seeking.[21]

48-base pair VNTR

The 48-base pair variable number tandem repeat (VNTR) in exon 3 range from 2 to 11 repeats.[16] Dopamine is more potent at the D4 receptor with 2 allelic repeat or 7 allelic repeats than the variant with 4 allelic repeats.[22]

DRD4-7R, the 7-repeat (7R) variant of DRD4 (DRD4 7-repeat polymorphism), has been linked to a susceptibility for developing ADHD in several meta-analyses and other psychological traits and disorders.[23][24] Adults and children with the DRD4 7-repeat polymorphism show variations in auditory-evoked gamma oscillations, which may be related to attention processing.[25][26]

The frequency of the alleles varies greatly between populations, e.g., the 7-repeat version has high incidence in America and low in Asia.[27] "Long" versions of polymorphisms are the alleles with 6 to 10 repeats. 7R appears to react less strongly to dopamine molecules.[28]

The 48-base pair VNTR has been the subject of much speculation about its evolution and role in human behaviors cross-culturally. The 7R allele appears to have been selected for about 40,000 years ago.[27] In 1999 Chen and colleagues[29] observed that populations who migrated farther in the past 30,000 to 1,000 years ago had a higher frequency of 7R/long alleles. They also showed that nomadic populations had higher frequencies of 7R alleles than sedentary ones. More recently it was observed that the health status of nomadic Ariaal men was higher if they had 7R alleles. However, in recently sedentary (non-nomadic) Ariaal those with 7R alleles seemed to have slightly deteriorated health.[30]

Novelty seeking

Despite early findings of an association between the DRD4 48bp VNTR and novelty seeking (a normal characteristic of exploratory and excitable people),[31][32] a 2008 meta-analysis compared 36 published studies of novelty seeking and the polymorphism and found no effect. Results are consistent with novelty-seeking behavior being a complex trait associated with many genes, and the variance attributable to DRD4 by itself being very small. The meta-analysis of 11 studies did find that another polymorphism in the gene, the -521C/T, showed an association with novelty seeking.[21] While human results are not strong, research in animals has suggested stronger associations [33][34][35][36][37][38] and new evidence suggests that human encroachment may exert selection pressure in favor of DRD4 variants associated with novelty seeking.[39]

Cognition

Several studies have shown that agonists that activate the D4 receptor increase working memory performance and fear acquisition in monkeys and rodents according to a U-shaped dose response curve.[40][41][42] However, antagonists of the D4 receptor reverse stress-induced or drug-induced working memory deficits.[43][44] Gamma oscillations, which may be correlated with cognitive processing, can be increased by D4R agonists, but are not significantly reduced by D4R antagonists.[45][46][47]

Cognitive development

Several studies have suggested that parenting may affect the cognitive development of children with the 7-repeat allele of DRD4.[39] Parenting that has maternal sensitivity, mindfulness, and autonomy–support at 15 months was found to alter children's executive functions at 18 to 20 months.[39] Children with poorer quality parenting were more impulsive and sensation seeking than those with higher quality parenting.[39] Higher quality parenting was associated with better executive control in 4-year-olds.[39]

Ligands
Chemical structures of representative D4-preferring ligands.

Agonists
  • WAY-100635: potent full agonist, with 5-HT1A antagonistic component[48]
  • A-412,997: full agonist, > 100-fold selective over a panel of seventy different receptors and ion channels[49]
  • ABT-724 - developed for treatment of erectile dysfunction[50]
  • ABT-670 - better oral bioavailability than ABT-724[51]
  • FAUC 316: partial agonist, > 8600-fold selective over other dopamine receptor subtypes[52]
  • FAUC 299: partial agonist[52]
  • F-15063: antipsychotic with partial D4 agonism
  • (E)-1-aryl-3-(4-pyridinepiperazin-1-yl)propanone oximes[53]
  • PIP3EA: partial agonist[54]
  • Flibanserin - partial agonist
  • PD-168,077 - D4 selective but also binds to α1A, α2C and 5HT1A
  • CP-226,269 - D4 selective but also binds to D2, D3, α2A, α2C and 5HT1A
  • Ro10-5824 – partial agonist
  • Roxindole – D4 selective but also D2 and D3 autoreceptor agonist, 5HT1A receptor agonist, serotonin reuptake inhibitor)
  • Apomorphine – D4 selective but also D2 and D3 agonist, α-adrenergic and serotonergic weak antagonist

Antagonists

Inverse agonists
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See also
  • dopamine hypothesis of psychosis

References
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