Associations between catechol-O-methyltransferase (COMT) genotypes at rs4818 and rs4680 and gene expression in human dorsolateral prefrontal cortex

• Published in: Experimental brain research 2020-02, Vol.238 (2), p.477-486
• Main Authors: Dean, Brian, Parkin, Georgia M., Gibbons, Andrew S.
• Format: Article
• Language: English
• Subjects: Biomedical and Life Sciences; Biomedicine; Biotechnology industry; Catechin; Catechol; Catechol O-methyltransferase; Cognition; Estrogen; Gene expression; Genes; Genetic aspects; Genotype; Genotype & phenotype; Genotypes; Homozygotes; Hypotheses; Kinases; Mental illness; Methyltransferase; Neurology; Neurophysiology; Neurosciences; Prefrontal cortex; Research Article; Single nucleotide polymorphisms; Single-nucleotide polymorphism; Synaptic plasticity; Transferases
• ISSN: 0014-4819; 1432-1106
• DOI: 10.1007/s00221-020-05730-0

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™ 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.