Journal
EXPERIMENTAL BRAIN RESEARCH
Volume 238, Issue 2, Pages 477-486Publisher
SPRINGER
DOI: 10.1007/s00221-020-05730-0
Keywords
Catechol-O-methyltransferase; Dorsolateral prefrontal cortex; Gene expression; Human postmortem CNS
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Funding
- CRC for Mental Health [N/A] Funding Source: Medline
- National Health and Medical Research Council [566967] Funding Source: Medline
- Victorian State Government [N/A] Funding Source: Medline
- Department of Education, Australian Government (AU) [N/A] Funding Source: Medline
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Having reported associations between catechol-O-methyltransferase (COMT) genotypes at SNPs rs4818 and rs4680 with levels of soluble COMT (S-COMT) in human dorsolateral prefrontal cortex (DLPFC), we postulated that changes in the levels of cortical S-COMT could impact on behavioural abilities associated with COMT genotype through S-COMT-mediated changes in gene expression. To test this hypothesis, we have examined the relationships between COMT genotypes and gene expression measured using the Affymetrix (TM) Human Exon 1.0 ST Array in the DLPFC from 141 individuals, some of whom had had a psychiatric disorder. There were significant differences in levels of expression of 15 genes between individuals with a homozygous genotype at rs4818 (GG vs CC), compared to differences in levels of expression of 6 genes between homozygotes at rs4680 (GG vs AA); levels of expression of CEP128, EFCAB13, and FAM133A differed between homozygotes at both SNPs. Fourteen of the genes differentially expressed in the DLPFC according to COMT genotypes have oestrogen receptor elements and their expression could, therefore, be regulated by catecholestrogens, which are substrates for COMT that occupy and activate oestrogen receptors. In addition, the changes in gene expression between the homozygotes at rs4818 or rs4680 would be expected to impact on neuronal function, synaptic plasticity, cognition, and attention. These data would support a hypothesis that the mechanism underlying the association between COMT genotype and cognition involves differential changes in cortical gene expression.
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