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Molecular and Cellular Mechanisms on Autism Spectrum Disorder

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Molecular Neurobiology".

Deadline for manuscript submissions: 30 June 2024 | Viewed by 2353

Special Issue Editor


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Guest Editor
Division of Child and Adolescent Neuropsychiatry, University Hospital of Siena, 53100 Siena, Italy
Interests: autism spectrum disorders; genetics and psychopharmacology

Special Issue Information

Dear Colleagues,

Autism spectrum disorder (ASD) is a group of neurodevelopmental disorders characterized by social and communication abnormalities. Synaptic abnormalities have been observed in preclinical ASD models. They are thought to play a major role in ASD and might be modified by targeted interventions. An imbalance in excitatory to inhibitory neurotransmission (E/I imbalance), through altered glutamatergic and GABAergic neurotransmission, respectively, is thought to be implicated in the pathogenesis of ASD. Molecular abnormalities in synaptic structures and functions in ASD involve neuroligins and neurexins, proteins that are crucial for aligning and activating synapses along with the SHANK3 scaffolding protein. Multiple genes can contribute to the disruption of GABAergic interneuron development and therefore are involved in ASD. Mutations in GABAA receptor subunit genes have also been described. The genes coding for the three GABAA receptor subunits α5, β3, and γ3 (GABRA5, GABRB3, and GABRG3, respectively) are located on the 15q11chromosome, and single-nucleotide polymorphisms (SNPs) in these genes have been associated with ASD. Neurexins (NRXNs) are presynaptic proteins that bind their postsynaptic counterparts, the neuroligins (NLGNs). NRXN–NLGN signaling is consistently involved in postsynaptic differentiation, and it controls the balance of inhibitory GABAergic and excitatory glutamatergic signaling. Mutations and chromosomal rearrangements in NRXN have been associated with ASD. Mutations in NLGN1, -3, and -4X genes have been identified in ASD as well. The aim of this topic is to contribute to disentangling the complex synaptic and molecular abnormalities of ASD and related new experimental treatments.

Dr. Roberto Canitano
Guest Editor

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Keywords

  • autism spectrum disorders
  • synaptic abnormalities
  • glutamatergic and GABA-targeted treatments

Published Papers (1 paper)

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Research

34 pages, 6625 KiB  
Article
Epigenetic Gene-Regulatory Loci in Alu Elements Associated with Autism Susceptibility in the Prefrontal Cortex of ASD
by Thanit Saeliw, Songphon Kanlayaprasit, Surangrat Thongkorn, Kwanjira Songsritaya, Bumpenporn Sanannam, Chanachai Sae-Lee, Depicha Jindatip, Valerie W. Hu and Tewarit Sarachana
Int. J. Mol. Sci. 2023, 24(8), 7518; https://doi.org/10.3390/ijms24087518 - 19 Apr 2023
Cited by 1 | Viewed by 1873
Abstract
Alu elements are transposable elements that can influence gene regulation through several mechanisms; nevertheless, it remains unclear whether dysregulation of Alu elements contributes to the neuropathology of autism spectrum disorder (ASD). In this study, we characterized transposable element expression profiles and their sequence [...] Read more.
Alu elements are transposable elements that can influence gene regulation through several mechanisms; nevertheless, it remains unclear whether dysregulation of Alu elements contributes to the neuropathology of autism spectrum disorder (ASD). In this study, we characterized transposable element expression profiles and their sequence characteristics in the prefrontal cortex tissues of ASD and unaffected individuals using RNA-sequencing data. Our results showed that most of the differentially expressed transposable elements belong to the Alu family, with 659 loci of Alu elements corresponding to 456 differentially expressed genes in the prefrontal cortex of ASD individuals. We predicted cis- and trans-regulation of Alu elements to host/distant genes by conducting correlation analyses. The expression level of Alu elements correlated significantly with 133 host genes (cis-regulation, adjusted p < 0.05) associated with ASD as well as the cell survival and cell death of neuronal cells. Transcription factor binding sites in the promoter regions of differentially expressed Alu elements are conserved and associated with autism candidate genes, including RORA. COBRA analyses of postmortem brain tissues showed significant hypomethylation in global methylation analyses of Alu elements in ASD subphenotypes as well as DNA methylation of Alu elements located near the RNF-135 gene (p < 0.05). In addition, we found that neuronal cell density, which was significantly increased (p = 0.042), correlated with the expression of genes associated with Alu elements in the prefrontal cortex of ASD. Finally, we determined a relationship between these findings and the ASD severity (i.e., ADI-R scores) of individuals with ASD. Our findings provide a better understanding of the impact of Alu elements on gene regulation and molecular neuropathology in the brain tissues of ASD individuals, which deserves further investigation. Full article
(This article belongs to the Special Issue Molecular and Cellular Mechanisms on Autism Spectrum Disorder)
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