Coexpression of Gene Transcripts with Monoamine Oxidase A Quantified by Human In Vivo Positron Emission Tomography

Cereb Cortex. 2022 Aug 3;32(16):3516-3524. doi: 10.1093/cercor/bhab430.

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.

Keywords: Allen Human Brain Atlas; MAO-A; antidepressant; molecular neuroimaging; transcriptomics.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Brain* / diagnostic imaging
  • Brain* / metabolism
  • Carbon Radioisotopes
  • Female
  • Harmine / metabolism
  • Humans
  • Monoamine Oxidase* / genetics
  • Monoamine Oxidase* / metabolism
  • Positron-Emission Tomography* / methods

Substances

  • Carbon Radioisotopes
  • Harmine
  • Monoamine Oxidase
  • monoamine oxidase A, human