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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container_title | Cerebral cortex (New York, N.Y. 1991) |
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creator | Godbersen, G M Murgaš, M Gryglewski, G Klöbl, M Unterholzner, J Rischka, L Spies, M Baldinger-Melich, P Winkler, D Lanzenberger, R |
description | 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. |
doi_str_mv | 10.1093/cercor/bhab430 |
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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.</description><identifier>ISSN: 1047-3211</identifier><identifier>ISSN: 1460-2199</identifier><identifier>EISSN: 1460-2199</identifier><identifier>DOI: 10.1093/cercor/bhab430</identifier><identifier>PMID: 34952543</identifier><language>eng</language><publisher>United States: Oxford University Press</publisher><subject>Adult ; Brain - diagnostic imaging ; Brain - metabolism ; Carbon Radioisotopes ; Female ; Harmine - metabolism ; Humans ; Monoamine Oxidase - genetics ; Monoamine Oxidase - metabolism ; Positron-Emission Tomography - methods</subject><ispartof>Cerebral cortex (New York, N.Y. 1991), 2022-08, Vol.32 (16), p.3516-3524</ispartof><rights>The Author(s) 2021. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com 2021</rights><rights>The Author(s) 2021. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c329t-530de5c44e090f0f2c15e9d2bf5edacc3abfc118d7c8be1c771f566e866f1da23</citedby><cites>FETCH-LOGICAL-c329t-530de5c44e090f0f2c15e9d2bf5edacc3abfc118d7c8be1c771f566e866f1da23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,1584,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34952543$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Godbersen, G M</creatorcontrib><creatorcontrib>Murgaš, M</creatorcontrib><creatorcontrib>Gryglewski, G</creatorcontrib><creatorcontrib>Klöbl, M</creatorcontrib><creatorcontrib>Unterholzner, J</creatorcontrib><creatorcontrib>Rischka, L</creatorcontrib><creatorcontrib>Spies, M</creatorcontrib><creatorcontrib>Baldinger-Melich, P</creatorcontrib><creatorcontrib>Winkler, D</creatorcontrib><creatorcontrib>Lanzenberger, R</creatorcontrib><title>Coexpression of gene transcripts with monoamine oxidase a quantified by human in vivo positron emission tomography</title><title>Cerebral cortex (New York, N.Y. 1991)</title><addtitle>Cereb Cortex</addtitle><description>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.</description><subject>Adult</subject><subject>Brain - diagnostic imaging</subject><subject>Brain - metabolism</subject><subject>Carbon Radioisotopes</subject><subject>Female</subject><subject>Harmine - metabolism</subject><subject>Humans</subject><subject>Monoamine Oxidase - genetics</subject><subject>Monoamine Oxidase - metabolism</subject><subject>Positron-Emission Tomography - methods</subject><issn>1047-3211</issn><issn>1460-2199</issn><issn>1460-2199</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkD1PwzAQQC0EoqWwMiKPMIT6I06aEVV8SZVYYI4c-9wYNXZqJ6X99wSlsDL5JL97Oj2Erim5p6TgcwVB-TCvalmlnJygKU0zkjBaFKfDTNI84YzSCbqI8ZMQmjPBztGEp4VgIuVTFJYe9m2AGK132Bu8Bge4C9JFFWzbRfxluxo33nnZ2OHL762WEbDE2166zhoLGlcHXPeNdNg6vLM7j1sfbRcGIzR2VHe-8esg2_pwic6M3ES4Or4z9PH0-L58SVZvz6_Lh1WiOCu6RHCiQag0BVIQQwxTVEChWWUEaKkUl5VRlC50rhYVUJXn1Igsg0WWGaol4zN0O3rb4Lc9xK4cblGw2UgHvo8ly2jKOGe8GND7EVXBxxjAlG2wjQyHkpLyp3M5di6PnYeFm6O7rxrQf_hv2AG4GwHft__JvgEqIY0_</recordid><startdate>20220803</startdate><enddate>20220803</enddate><creator>Godbersen, G M</creator><creator>Murgaš, M</creator><creator>Gryglewski, G</creator><creator>Klöbl, M</creator><creator>Unterholzner, J</creator><creator>Rischka, L</creator><creator>Spies, M</creator><creator>Baldinger-Melich, P</creator><creator>Winkler, D</creator><creator>Lanzenberger, R</creator><general>Oxford University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20220803</creationdate><title>Coexpression of gene transcripts with monoamine oxidase a quantified by human in vivo positron emission tomography</title><author>Godbersen, G M ; Murgaš, M ; Gryglewski, G ; Klöbl, M ; Unterholzner, J ; Rischka, L ; Spies, M ; Baldinger-Melich, P ; Winkler, D ; Lanzenberger, R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c329t-530de5c44e090f0f2c15e9d2bf5edacc3abfc118d7c8be1c771f566e866f1da23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Adult</topic><topic>Brain - diagnostic imaging</topic><topic>Brain - metabolism</topic><topic>Carbon Radioisotopes</topic><topic>Female</topic><topic>Harmine - metabolism</topic><topic>Humans</topic><topic>Monoamine Oxidase - genetics</topic><topic>Monoamine Oxidase - metabolism</topic><topic>Positron-Emission Tomography - methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Godbersen, G M</creatorcontrib><creatorcontrib>Murgaš, M</creatorcontrib><creatorcontrib>Gryglewski, G</creatorcontrib><creatorcontrib>Klöbl, M</creatorcontrib><creatorcontrib>Unterholzner, J</creatorcontrib><creatorcontrib>Rischka, L</creatorcontrib><creatorcontrib>Spies, M</creatorcontrib><creatorcontrib>Baldinger-Melich, P</creatorcontrib><creatorcontrib>Winkler, D</creatorcontrib><creatorcontrib>Lanzenberger, R</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Cerebral cortex (New York, N.Y. 1991)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Godbersen, G M</au><au>Murgaš, M</au><au>Gryglewski, G</au><au>Klöbl, M</au><au>Unterholzner, J</au><au>Rischka, L</au><au>Spies, M</au><au>Baldinger-Melich, P</au><au>Winkler, D</au><au>Lanzenberger, R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Coexpression of gene transcripts with monoamine oxidase a quantified by human in vivo positron emission tomography</atitle><jtitle>Cerebral cortex (New York, N.Y. 1991)</jtitle><addtitle>Cereb Cortex</addtitle><date>2022-08-03</date><risdate>2022</risdate><volume>32</volume><issue>16</issue><spage>3516</spage><epage>3524</epage><pages>3516-3524</pages><issn>1047-3211</issn><issn>1460-2199</issn><eissn>1460-2199</eissn><abstract>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.</abstract><cop>United States</cop><pub>Oxford University Press</pub><pmid>34952543</pmid><doi>10.1093/cercor/bhab430</doi><tpages>9</tpages></addata></record> |
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subjects | Adult Brain - diagnostic imaging Brain - metabolism Carbon Radioisotopes Female Harmine - metabolism Humans Monoamine Oxidase - genetics Monoamine Oxidase - metabolism Positron-Emission Tomography - methods |
title | Coexpression of gene transcripts with monoamine oxidase a quantified by human in vivo positron emission tomography |
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