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Haploinsufficiency of the Attention-Deficit/Hyperactivity Disorder Risk Gene St3gal3 in Mice Causes Alterations in Cognition and Expression of Genes Involved in Myelination and Sialylation

Zitieren Sie bitte immer diese URN: urn:nbn:de:bvb:20-opus-246855
  • Genome wide association meta-analysis identified ST3GAL3, a gene encoding the beta-galactosidase-alpha-2,3-sialyltransferase-III, as a risk gene for attention-deficit/hyperactivity disorder (ADHD). Although loss-of-function mutations in ST3GAL3 are implicated in non-syndromic autosomal recessive intellectual disability (NSARID) and West syndrome, the impact of ST3GAL3 haploinsufficiency on brain function and the pathophysiology of neurodevelopmental disorders (NDDs), such as ADHD, is unknown. Since St3gal3 null mutant mice display severeGenome wide association meta-analysis identified ST3GAL3, a gene encoding the beta-galactosidase-alpha-2,3-sialyltransferase-III, as a risk gene for attention-deficit/hyperactivity disorder (ADHD). Although loss-of-function mutations in ST3GAL3 are implicated in non-syndromic autosomal recessive intellectual disability (NSARID) and West syndrome, the impact of ST3GAL3 haploinsufficiency on brain function and the pathophysiology of neurodevelopmental disorders (NDDs), such as ADHD, is unknown. Since St3gal3 null mutant mice display severe developmental delay and neurological deficits, we investigated the effects of partial inactivation of St3gal3 in heterozygous (HET) knockout (St3gal3±) mice on behavior as well as expression of markers linked to myelination processes and sialylation pathways. Our results reveal that male St3gal3 HET mice display cognitive deficits, while female HET animals show increased activity, as well as increased cognitive control, compared to their wildtype littermates. In addition, we observed subtle alterations in the expression of several markers implicated in oligodendrogenesis, myelin formation, and protein sialylation as well as cell adhesion/synaptic target glycoproteins of ST3GAL3 in a brain region- and/or sex-specific manner. Taken together, our findings indicate that haploinsufficiency of ST3GAL3 results in a sex-dependent alteration of cognition, behavior and markers of brain plasticity.zeige mehrzeige weniger

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Autor(en): Olga Rivero, Judit Alhama-Riba, Hsing-Ping Ku, Matthias Fischer, Gabriela Ortega, Péter Álmos, David Diouf, Daniel van den Hove, Klaus-Peter Lesch
URN:urn:nbn:de:bvb:20-opus-246855
Dokumentart:Artikel / Aufsatz in einer Zeitschrift
Institute der Universität:Medizinische Fakultät / Klinik und Poliklinik für Psychiatrie, Psychosomatik und Psychotherapie
Medizinische Fakultät / Lehrstuhl für Molekulare Psychiatrie
Sprache der Veröffentlichung:Englisch
Titel des übergeordneten Werkes / der Zeitschrift (Englisch):Frontiers in Genetics
ISSN:1664-8021
Erscheinungsjahr:2021
Band / Jahrgang:12
Aufsatznummer:688488
Originalveröffentlichung / Quelle:Frontiers in Genetics (2021) 12:688488. doi: 10.3389/fgene.2021.688488
DOI:https://doi.org/10.3389/fgene.2021.688488
Allgemeine fachliche Zuordnung (DDC-Klassifikation):6 Technik, Medizin, angewandte Wissenschaften / 61 Medizin und Gesundheit / 610 Medizin und Gesundheit
Freie Schlagwort(e):attention-deficit/hyperactivity disorder (ADHD); hippocampus; mouse model; prefrontal cortex; psychiatric disorders; sialic acid; sialyltransferase
Datum der Freischaltung:10.02.2022
Datum der Erstveröffentlichung:28.09.2021
EU-Projektnummer / Contract (GA) number:953327
EU-Projektnummer / Contract (GA) number:728018
EU-Projektnummer / Contract (GA) number:FKZ01EW1902
OpenAIRE:OpenAIRE
Open-Access-Publikationsfonds / Förderzeitraum 2021
Lizenz (Deutsch):License LogoCC BY: Creative-Commons-Lizenz: Namensnennung 4.0 International