PuSH - Publication Server of Helmholtz Zentrum München

Schob, C.* ; Morellini, F.* ; Ohana, O.* ; Bakota, L.* ; Hrynchak, M.V.* ; Brandt, R.* ; Brockmann, M.D.* ; Cichon, N.* ; Hartung, H.* ; Hanganu-Opatz, I.L.* ; Kraus, V.* ; Scharf, S.* ; Herrmans-Borgmeyer, I.* ; Schweizer, M.* ; Kuhl, D.* ; Wöhr, M.* ; Vörckel, K.J.* ; Calzada-Wack, J. ; Fuchs, H. ; Gailus-Durner, V. ; Hrabě de Angelis, M. ; Garner, C.C.* ; Kreienkamp, H.J.* ; Kindler, S.*

Cognitive impairment and autistic-like behaviour in SAPAP4-deficient mice.

Transl. Psychiatry 9:7 (2019)
Publ. Version/Full Text DOI PMC
Open Access Gold
Creative Commons Lizenzvertrag
In humans, genetic variants of DLGAP1-4 have been linked with neuropsychiatric conditions, including autism spectrum disorder (ASD). While these findings implicate the encoded postsynaptic proteins, SAPAP1-4, in the etiology of neuropsychiatric conditions, underlying neurobiological mechanisms are unknown. To assess the contribution of SAPAP4 to these disorders, we characterized SAPAP4-deficient mice. Our study reveals that the loss of SAPAP4 triggers profound behavioural abnormalities, including cognitive deficits combined with impaired vocal communication and social interaction, phenotypes reminiscent of ASD in humans. These behavioural alterations of SAPAP4-deficient mice are associated with dramatic changes in synapse morphology, function and plasticity, indicating that SAPAP4 is critical for the development of functional neuronal networks and that mutations in the corresponding human gene, DLGAP4, may cause deficits in social and cognitive functioning relevant to ASD-like neurodevelopmental disorders.
Altmetric
Additional Metrics?
Edit extra informations Login
Publication type Article: Journal article
Document type Scientific Article
Corresponding Author
Keywords Obsessive-compulsive Disorder; Knockout Mouse Model; Synaptic Plasticity; Hippocampal; Proteins; Communication; Mutations; Deletion; Variants; Localization
ISSN (print) / ISBN 2158-3188
e-ISSN 2158-3188
Quellenangaben Volume: 9, Issue: 1, Pages: , Article Number: 7 Supplement: ,
Publisher Nature Publishing Group
Publishing Place Macmillan Building, 4 Crinan St, London N1 9xw, England
Non-patent literature Publications
Reviewing status Peer reviewed