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Allele C-specific methylation of the 5-HT2A receptor gene: Evidence for correlation with its expression and expression of DNA methylaseDNMT1
- Source :
- Journal of Neuroscience Research. 83:362-373
- Publication Year :
- 2006
- Publisher :
- Wiley, 2006.
-
Abstract
- Differential DNA methylation has been suggested to contribute to differential activity of alleles C and T and thereby to genetic associations between the C/T(102) polymorphism in the 5-HT2A receptor gene (5HT2AR) and psychiatric disorders. We surveyed methylation in two CpG sites, which are specific to allele C. The majority of allele C-specific CpG sites were methylated in human temporal cortex and peripheral leukocytes and levels of methylation varied between individuals. Levels of methylation in the promoter correlated significantly with the expression of 5HT2AR. Methylation of allele C-specific CpG sites in the first exon correlated significantly with the expression of DNA methylase 1 (DNMT1) but not S-adenosylhomocysteine hydrolase (AHCY). These findings support the hypothesis that allele-specific DNA methylation is involved in regulation of 5HT2AR expression, influencing expression differences between alleles C and T.
- Subjects :
- Adult
DNA (Cytosine-5-)-Methyltransferase 1
Male
Time Factors
Statistics as Topic
Gene Expression
Biology
Cellular and Molecular Neuroscience
Humans
Receptor, Serotonin, 5-HT2A
DNA (Cytosine-5-)-Methyltransferases
RNA, Messenger
Epigenetics
Allele
Promoter Regions, Genetic
Gene
Alleles
Genetics
Temporal cortex
Analysis of Variance
Base Sequence
Reverse Transcriptase Polymerase Chain Reaction
Brain
Exons
Methylation
DNA Methylation
Middle Aged
Molecular biology
Differentially methylated regions
Gene Expression Regulation
CpG site
Postmortem Changes
DNA methylation
CpG Islands
Female
Subjects
Details
- ISSN :
- 10974547 and 03604012
- Volume :
- 83
- Database :
- OpenAIRE
- Journal :
- Journal of Neuroscience Research
- Accession number :
- edsair.doi.dedup.....052947853bbf4848d04d3acfb9f821ac
- Full Text :
- https://doi.org/10.1002/jnr.20732