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• W2905504964 abstract "Transcriptomic analyses of postmortem brains have begun to elucidate molecular abnormalities in autism spectrum disorder (ASD). However, a crucial pathway involved in synaptic development, RNA editing, has not yet been studied on a genome-wide scale. Here we profiled global patterns of adenosine-to-inosine (A-to-I) editing in a large cohort of postmortem brains of people with ASD. We observed a global bias for hypoediting in ASD brains, which was shared across brain regions and involved many synaptic genes. We show that the Fragile X proteins FMRP and FXR1P interact with RNA-editing enzymes (ADAR proteins) and modulate A-to-I editing. Furthermore, we observed convergent patterns of RNA-editing alterations in ASD and Fragile X syndrome, establishing this as a molecular link between these related diseases. Our findings, which are corroborated across multiple data sets, including dup15q (genomic duplication of 15q11.2-13.1) cases associated with intellectual disability, highlight RNA-editing dysregulation in ASD and reveal new mechanisms underlying this disorder. An overall downregulation of RNA editing was observed in postmortem brains from people with autism, which was consistent across brain regions and genetic disorder subtypes. These changes were regulated by the RNA-binding proteins FMRP and FXR1P." @default.
• W2905504964 created "2018-12-22" @default.
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• W2905504964 date "2018-12-17" @default.
• W2905504964 modified "2023-10-16" @default.
• W2905504964 title "Widespread RNA editing dysregulation in brains from autistic individuals" @default.
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• W2905504964 doi "https://doi.org/10.1038/s41593-018-0287-x" @default.
• W2905504964 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6375307" @default.
• W2905504964 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/30559470" @default.
• W2905504964 hasPublicationYear "2018" @default.
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