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Do Autism Spectrum and Autoimmune Disorders Share Predisposition Gene Signature Due to mTOR Signaling Pathway Controlling Expression?

机译:自闭症频谱和自身免疫紊乱是否由于MTOR信号通路控制表达式而共享易感基因签名?

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摘要

Autism spectrum disorder (ASD) is characterized by uncommon genetic heterogeneity and a high heritability concurrently. Most autoimmune disorders (AID), similarly to ASD, are characterized by impressive genetic heterogeneity and heritability. We conducted gene-set analyses and revealed that 584 out of 992 genes (59%) included in a new release of the SFARI Gene database and 439 out of 871 AID-associated genes (50%) could be attributed to one of four groups: 1. FMRP (fragile X mental retardation protein) target genes, 2. mTOR signaling network genes, 3. mTOR-modulated genes, and 4. vitamin D3-sensitive genes. With the exception of FMRP targets, which are obviously associated with the direct involvement of local translation disturbance in the pathological mechanisms of ASD, the remaining categories are represented among AID genes in a very similar percentage as among ASD predisposition genes. Thus, mTOR signaling pathway genes make up 4% of ASD and 3% of AID genes, mTOR-modulated genes—31% of both ASD and AID genes, and vitamin D-sensitive genes—20% of ASD and 23% of AID genes. The network analysis revealed 3124 interactions between 528 out of 729 AID genes for the 0.7 cutoff, so the great majority (up to 67%) of AID genes are related to the mTOR signaling pathway directly or indirectly. Our present research and available published data allow us to hypothesize that both a certain part of ASD and AID comprise a connected set of disorders sharing a common aberrant pathway (mTOR signaling) rather than a vast set of different disorders. Furthermore, an immune subtype of the autism spectrum might be a specific type of autoimmune disorder with an early manifestation of a unique set of predominantly behavioral symptoms.
机译:自闭症谱系障碍(ASD)的特征在于罕见的遗传异质性和高遗传性。与ASD类似的自身免疫紊乱(AID)的特征在于令人印象深刻的遗传异质性和遗传性。我们进行了基因集分析,并显示出992个基因(59%)中的584个含量,包括在SFARI基因数据库的新释放中,871个援助相关基因中的439个(50%)可归因于四组中的一个: 1. FMRP(易碎X精神迟发蛋白)靶基因,2. MTOR信号传导网络基因,3. MTOR调制基因和4.维生素D3敏感基因。除FMRP目标外,显然与当地翻译干扰的直接涉及ASD的病理机制,剩余类别在援助基因中以非常相似的百分比表示,如ASD易感性基因。因此,MTOR信号传导途径基因占ASD的4%和3%的辅助基因,MTOR调制基因-31%的ASD和辅助基因的31%,维生素D敏感基因-20%的ASD和23%的援助基因。网络分析显示为0.7截止的729个援助基因中的528个相互作用,因此大多数(高达67%)的助剂直接或间接地与MTOR信号通路有关。我们目前的研究和可用的已发布数据允许我们假设ASD和AID的某一部分包括共享常见的异常途径(MTOR信令)而不是一组不同的不同障碍的一组连接的障碍。此外,自闭症谱的免疫亚型可能是一种特异性自身免疫疾病,具有初始表现的独特行为症状。

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