The human serotonin receptor 2B: coding region polymorphisms and association with vulnerability to illegal drug abuse
Jazyk angličtina Země Anglie, Velká Británie Médium print
Typ dokumentu srovnávací studie, časopisecké články, Research Support, U.S. Gov't, P.H.S.
PubMed
15608559
DOI
10.1097/00008571-200412000-00003
PII: 00008571-200412000-00003
Knihovny.cz E-zdroje
- MeSH
- alely MeSH
- běloši genetika MeSH
- dospělí MeSH
- frekvence genu MeSH
- genetická variace MeSH
- genetické markery MeSH
- glycin metabolismus MeSH
- jednonukleotidový polymorfismus * MeSH
- kodon MeSH
- kohortové studie MeSH
- lidé MeSH
- mikrosatelitní repetice MeSH
- poruchy spojené s užíváním psychoaktivních látek genetika MeSH
- receptor serotoninový 5-HT2B genetika MeSH
- sekvenční analýza DNA MeSH
- substituce aminokyselin MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- Research Support, U.S. Gov't, P.H.S. MeSH
- srovnávací studie MeSH
- Názvy látek
- genetické markery MeSH
- glycin MeSH
- kodon MeSH
- receptor serotoninový 5-HT2B MeSH
OBJECTIVE AND METHODS: 5-Hydroxytryptamine (serotonin) receptor 2B (HTR2B) is involved in brain development. Although expressed in the human brain, HTR2B has not been investigated much for its role in higher brain functions. Here we describe a genome-scan with 391 simple sequence repeat markers in 300 Caucasians, identifying HTR2B gene as a candidate for drug abuse vulnerability. RESULTS: From DNA re-sequencing of 110 subjects, we discovered three novel single nucleotide polymorphisms (SNPs), two of which confer a double-mutant of the receptor protein in a drug-abusing population. Arg6, a conserved basic residue, and the conserved acidic Glu42 are mutated simultaneously into Gly, termed R6G/E42G. Furthermore, this double-mutant tends to associate with drug abuse (P = 0.08 by chi2 test). The third SNP that is a synonymous mutation in the codon of Gln11 showed significant association with drug abuse (P = 0.0335 by Fisher's exact test). CONCLUSION: Our data are the first suggesting that HTR2B contributes to brain architecture and pathways that are involved in illegal drug reward.
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