Coexpression of gene transcripts with monoamine oxidase a quantified by human in vivo positron emission tomography

Abstract The monoamine oxidase A (MAO-A) is integral to monoamine metabolism and is thus relevant to the pathophysiology of various neuropsychiatric disorders; however, associated gene-enzyme relations are not well understood. This study aimed to unveil genes coexpressed with MAO-A. Therefore, 18 17...

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Veröffentlicht in:Cerebral cortex (New York, N.Y. 1991) N.Y. 1991), 2022-08, Vol.32 (16), p.3516-3524
Hauptverfasser: Godbersen, G M, Murgaš, M, Gryglewski, G, Klöbl, M, Unterholzner, J, Rischka, L, Spies, M, Baldinger-Melich, P, Winkler, D, Lanzenberger, R
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Sprache:eng
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Zusammenfassung:Abstract The monoamine oxidase A (MAO-A) is integral to monoamine metabolism and is thus relevant to the pathophysiology of various neuropsychiatric disorders; however, associated gene-enzyme relations are not well understood. This study aimed to unveil genes coexpressed with MAO-A. Therefore, 18 179 mRNA expression maps (based on the Allen Human Brain Atlas) were correlated with the cerebral distribution volume (VT) of MAO-A assessed in 36 healthy subjects (mean age ± standard deviation: 32.9 ± 8.8 years, 18 female) using [11C]harmine positron emission tomography scans. Coexpression analysis was based on Spearman’s ρ, over-representation tests on Fisher’s exact test with false discovery rate (FDR) correction. The analysis revealed 35 genes in cortex (including B-cell translocation gene family, member 3, implicated in neuroinflammation) and 247 genes in subcortex (including kallikrein-related peptidase 10, implicated in Alzheimer’s disease). Significantly over-represented Gene Ontology terms included “neuron development”, “neuron differentiation”, and “cell-cell signaling” as well as “axon” and “neuron projection”. In vivo MAO-A enzyme distribution and MAOA expression did not correlate in cortical areas (ρ = 0.08) while correlation was found in subcortical areas (ρ = 0.52), suggesting influences of region-specific post-transcriptional and -translational modifications. The herein reported information could contribute to guide future genetic studies, deepen the understanding of associated pathomechanisms and assist in the pursuit of novel therapeutic targets.
ISSN:1047-3211
1460-2199
1460-2199
DOI:10.1093/cercor/bhab430