Translational PsychiatryNeurosciencePeer-reviewed journal article
Structural and Functional Brain-wide Alterations in A350V IQSEC2 Mutant Mice Displaying Autistic-like Behavior
Daniela LichtmaniD, Eyal BergmanniD, Alexandra KavushanskyiD, Nadav CoheniD, Nina S. Levy, Andrew P. LevyiD, Itamar KahniD
Abstract
IQSEC2 is an X-linked gene which is associated with autism spectrum disorder (ASD), intellectual disability and epilepsy. IQSEC2 is a postsynaptic density protein, localized on excitatory synapses as part of the NMDA receptor complex and is suggested to play a role in AMPA receptor trafficking and mediation of long-term depression. Here, we present brain-wide structural volumetric and functional connectivity characterization in a novel mouse model with a missense mutation in the IQ domain of IQSEC2 (A350V). Using high-resolution structural and functional MRI, we show that animals with the A350V mutation display increased whole-brain volume which was further found to be specific to the cortex and hippocampus. Moreover, using a data-driven approach we demonstrate that A350V mice present alterations in structure-function relations of the frontal, auditory, and visual networks. Examination of these alterations revealed an increase in functional connectivity between the anterior cingulate cortex and the dorsomedial striatum. We also show that corticostriatal functional connectivity is correlated with individual variability in social behavior only in A350V mice, as assessed using the three-chamber social preference test. Our results at the systems-level bridge the impact of previously reported changes in AMPA receptor trafficking to network-level disruption and impaired social behavior. Further, the A350V mouse model recapitulates similarly reported brain-wide changes in other ASD mouse models, with substantially different cellular-level pathologies that nonetheless result in similar brain-wide alterations, suggesting that novel therapeutic approaches in ASD that result in systems-level rescue will be relevant to IQSEC2 mutations. Significance StatementSeveral recent studies have characterized the changes in the organization of brain networks in animal models of autism spectrum disorders (ASD). Here we assessed the effect of an A350V missense mutation in the IQSEC2 gene, which is associated with ASD, on brain-wide functional connectivity and its relation to social behavior deficits in A350V mice relative to controls. We found that the A350V IQSEC2 model results in disrupted functional connectivity of the anterior cingulate cortex and the dorsomedial striatum. Critically, disrupted increased corticostriatal functional connectivity is predictive of individual variability in social interaction only in A350V mice implicating this pathway in the pathophysiology of the A350V IQSEC2 mutation.
- organism: mouse
- assay: imaging
- research focus: cell-cell communication
- research focus: spatial domain detection
- approach: experimental assay
- Citations
- 13
- FWCI
- 1.05
- Field percentile
- top 28%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Precision medicine for the rescue of specific impairments in social behavior associated with the A350V Iqsec2 mutation
Renad Jabarin, Nina S. Levy, … Shlomo Wagner·bioRxiv·Nov 4, 2020
- Autism-associated SCN2A deficiency disrupts cortico-striatal circuitry in human brain assembloids
Xiaoling Chen, Jingliang Zhang, … Yang Yang·NeuronPeer-reviewed·Sep 1, 2026
- A cross-species link between mTOR-related synaptic pathology and functional hyperconnectivityin autism
Marco Pagani, Noemi Barsotti, … Alessandro Gozzi·Nature CommunicationsPeer-reviewed·Oct 19, 2021
- Selective Shank3 Deletion in Glutamatergic Neurons of the Anterior Insular Cortex Induces Autism-Related Behavior and Circuit Dysfunction
Paula Mut-Arbona, Guilherme Horta, … Elena Martín‐García·bioRxiv·Apr 1, 2026
- AUTS2 gene dosage affects synaptic AMPA receptors via a local dendritic spine AUTS2-TTC3-AKT-mTORC1 signaling dysfunction
Aude-Marie Lepagnol-Bestel, Arnaud Duchon, … Michel Simonneau·bioRxiv·Dec 1, 2022
- Homozygous loss of autism-risk gene CNTNAP2 results in reduced local and long-range prefrontal functional connectivity
Adam Liska, Alice Bertero, … Alessandro Gozzi·Cerebral CortexPeer-reviewed·Jan 30, 2017