Abstract summary 

Epigenetics makes substantial contribution to the aetiology of autism spectrum disorder (ASD) and may harbour a unique opportunity to prevent the development of ASD. We aimed to identify novel epigenetic genes involved in ASD aetiology.Trio-based whole exome sequencing was conducted on ASD families. Genome editing technique was used to knock out the candidate causal gene in a relevant cell line. ATAC-seq, ChIP-seq and RNA-seq were performed to investigate the functional impact of knockout (KO) or mutation in the candidate gene.We identified a novel candidate gene (nuclear autoantigenic sperm protein) for epigenetic dysregulation in ASD in a Chinese nuclear family including one proband with autism and comorbid atopic disease. The de novo likely gene disruptive variant t(Q289X) subjects the expression of t to nonsense-mediated decay. t KO increases chromatin accessibility, promotes the active promoter state of genes enriched in synaptic signalling and leads to upregulated expression of genes in the neural signalling and immune signalling pathways. Compared with wild-type t, t(Q289X) enhances chromatin accessibility of the genes with enriched expression in the brain. RNA-seq revealed that genes involved in neural and immune signalling are affected by the t mutation, consistent with the phenotypic impact and molecular effects of nasp-1 mutations in . Two additional patients with ASD were found carrying deletion or deleterious mutation in the gene.We identified novel epigenetic mechanisms mediated by t which may contribute to the pathogenesis of ASD and its immune comorbidity.

Authors & Co-authors:  Zhang Yang Ji Meng Zhu Zheng Glessner Qu Cui Liu Wang Li Zhang Xiu Sun Sun Li Hakonarson Li Xia

Study Outcome 

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