Abstract

BackgroundThe genetics of autism spectrum disorder (hereafter referred to as “autism”) are rapidly unfolding, with a significant increase in the identification of genes implicated in the disorder. Many of these genes are part of a complex landscape of genetic variants that are thought to act together to cause the behavioral phenotype associated with autism. One of the few single-locus causes of autism involves a mutation in the SH3 and multiple ankyrin repeat domains 3 (SHANK3) gene. Previous electrophysiological studies in mice with Shank3 mutations demonstrated impairment in synaptic long-term potentiation, suggesting a potential disruption at the synapse.MethodsTo understand how variants in SHANK3 would lead to such impairments and manifest in the brain of patients with autism, we assessed the presence of synaptic pathology in Shank3-deficient mice at 5 weeks and 3 months of age, focusing on the stratum radiatum of the CA1 field. This study analyzed both Shank3 heterozygous and homozygous mice using an electron microscopy approach to determine whether there is a morphological correlate to the synaptic functional impairment.ResultsAs both synaptic strength and plasticity are affected in Shank3-deficient mice, we hypothesized that there would be a reduction in synapse density, postsynaptic density length, and perforated synapse density. No differences were found in most parameters assessed. However, Shank3 heterozygotes had significantly higher numbers of perforated synapses at 5 weeks compared to 3 months of age and significantly higher numbers of perforated synapses compared to 5-week-old wildtype and Shank3 homozygous mice.ConclusionsAlthough this finding represents preliminary evidence for ultrastructural alterations, it suggests that while major structural changes seem to be compensated for in Shank3-deficient mice, more subtle morphological alterations, affecting synaptic structure, may take place in an age-dependent manner.

Highlights

  • IntroductionThe genetics of autism spectrum disorder (hereafter referred to as “autism”) are rapidly unfolding, with a significant increase in the identification of genes implicated in the disorder

  • The genetics of autism spectrum disorder are rapidly unfolding, with a significant increase in the identification of genes implicated in the disorder

  • No difference was found in synapse density between Shank3 heterozygous, Shank3 homozygous, and wildtype 5-week-old mice (F(2,12) = 1.915, p = 0.19; Fig. 2a)

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Summary

Introduction

The genetics of autism spectrum disorder (hereafter referred to as “autism”) are rapidly unfolding, with a significant increase in the identification of genes implicated in the disorder. Many of these genes are part of a complex landscape of genetic variants that are thought to act together to cause the behavioral phenotype associated with autism. Patients with 22q13 deletions have varying deletion sizes, SHANK3 is a gene that has been consistently implicated [12] and was later found to be exclusively affected through point mutations in some individuals with PMS [10, 13,14,15], leading to the conclusion that this gene is likely a strong candidate gene for autism as well. Given its crucial role in the etiology of PMS and autism, studying the impact of a loss of SHANK3 will allow for a detailed assessment of cellular and molecular mechanisms that underlie pathology

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