The human serotonin receptor 2B: coding region polymorphisms and association with vulnerability to illegal drug abuse
Language English Country Great Britain, England Media print
Document type Comparative Study, Journal Article, Research Support, U.S. Gov't, P.H.S.
PubMed
15608559
DOI
10.1097/00008571-200412000-00003
PII: 00008571-200412000-00003
Knihovny.cz E-resources
- MeSH
- Alleles MeSH
- White People genetics MeSH
- Adult MeSH
- Gene Frequency MeSH
- Genetic Variation MeSH
- Genetic Markers MeSH
- Glycine metabolism MeSH
- Polymorphism, Single Nucleotide * MeSH
- Codon MeSH
- Cohort Studies MeSH
- Humans MeSH
- Microsatellite Repeats MeSH
- Substance-Related Disorders genetics MeSH
- Receptor, Serotonin, 5-HT2B genetics MeSH
- Sequence Analysis, DNA MeSH
- Amino Acid Substitution MeSH
- Check Tag
- Adult MeSH
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, U.S. Gov't, P.H.S. MeSH
- Comparative Study MeSH
- Names of Substances
- Genetic Markers MeSH
- Glycine MeSH
- Codon MeSH
- Receptor, Serotonin, 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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