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Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders

机译:在两个独立的基于家庭的样本中的基因本体论富集分析突出了自闭症谱系障碍的生物学上合理的过程

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摘要

Recent genome-wide association studies (GWAS) have implicated a range of genes from discrete biological pathways in the aetiology of autism. However, despite the strong influence of genetic factors, association studies have yet to identify statistically robust, replicated major effect genes or SNPs. We apply the principle of the SNP ratio test methodology described by O'Dushlaine et al to over 2100 families from the Autism Genome Project (AGP). Using a two-stage design we examine association enrichment in 5955 unique gene-ontology classifications across four groupings based on two phenotypic and two ancestral classifications. Based on estimates from simulation we identify excess of association enrichment across all analyses. We observe enrichment in association for sets of genes involved in diverse biological processes, including pyruvate metabolism, transcription factor activation, cell-signalling and cell-cycle regulation. Both genes and processes that show enrichment have previously been examined in autistic disorders and offer biologically plausibility to these findings.
机译:最近的全基因组关联研究(GWAS)牵涉到自闭症病因的离散生物学途径中的一系列基因。但是,尽管遗传因素的影响很大,但关联研究尚未确定统计学上可靠的,复制的主要效应基因或SNP。我们将O'Dushlaine等人描述的SNP比率测试方法的原理应用于自闭症基因组计划(AGP)的2100多个家庭。使用两阶段设计,我们基于两个表型和两个祖先分类,在四个分组中检查了5955个独特的基因本体论分类中的关联富集。基于模拟的估计,我们在所有分析中都发现过多的关联富集。我们观察到涉及各种生物过程的基因集的富集,包括丙酮酸代谢,转录因子激活,细胞信号传导和细胞周期调控。以前已经在自闭症中检查了显示富集的基因和过程,并为这些发现提供了生物学上的合理性。

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