Alteration of Trim33 Expression at Transcriptional and Translational Levels Is Correlated With Autism Symptoms Publisher Pubmed



Norouzi Ofogh S¹ ; Rasoolijazi H^{1, 2, 3} ; Shahsavand Ananloo E^{4, 5} ; Shahrivar Z⁶ ; Joghataei MT^{2, 3, 7} ; Sadeghi B⁸ ; Bozorgmehr A⁹ ; Alizadeh F⁴ Show Affiliations
Source: Journal of Molecular Neuroscience Published:2021

Abstract

As a complex neurodevelopmental disorder, autism affects children in three major cognitive domains including social interactions, language learning and repetitive stereotyped behaviors. Abnormal regulation of cell proliferation in the brain during the embryonic period via the TGF-β signaling pathway and TRIM33 gene that encodes a protein with a corepressor and regulatory role in this pathway has been considered as an etiology for autism. Here, we investigated the association of a variation of TRIM33 with autism symptoms at levels of mRNA and protein expression. We used Autism Diagnostic Interview-Revised (ADI-R) and Childhood Autism Rating Scale (CARS) as behavioral diagnostic tools. Normal and autistic children were genotyped for a TRIM33 polymorphism (rs11102807), and then expression was assessed at transcriptional and translational levels. Results demonstrated that the frequency of the homozygous A allele (AA genotype of rs11102807) was significantly higher in children with autism (P < 0.001), whereas carriers of the G allele were mostly among healthy individuals. Children homozygous for the rs11102807 A allele were associated with an increase in CARS and ADI-R scores, indicating a significant correlation with autism symptoms. TRIM33 gene expression at both mRNA (P < 0.01) and protein (P < 0.001) levels was significantly higher in controls compared to autistic children. A remarkable association between higher TRIM33 gene expression at the transcriptional level and lower scores for both CARS and ADI-R was observed in non-autistic children. It seems that rs11102807 modulates the function and expression of the TRIM33 gene, implying that the A allele may increase the risk of autism in children by reducing gene expression and altering the TGF-β signaling pathway. © 2021, The Author(s), under exclusive licence to Springer Science+Business Media, LLC part of Springer Nature.