剪接特异性全转录组关联发现精神分裂症的遗传机制。

IF 8.1 1区 生物学 Q1 GENETICS & HEREDITY
American journal of human genetics Pub Date : 2024-08-08 Epub Date: 2024-06-25 DOI:10.1016/j.ajhg.2024.06.001
Jonatan L Hervoso, Kofi Amoah, Jack Dodson, Mudra Choudhury, Arjun Bhattacharya, Giovanni Quinones-Valdez, Bogdan Pasaniuc, Xinshu Xiao
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引用次数: 0

摘要

最近的研究强调了 RNA 剪接这一替代 RNA 处理的关键机制在建立遗传变异与疾病之间的联系中的重要作用。影响 RNA 剪接变异的基因位点对复杂性状的影响相当大,可能超过了影响总基因表达的位点。RNA 剪接失调已成为神经和精神疾病的一个主要潜在诱因,这可能是由于人脑中的交替剪接基因异常普遍。然而,在基因改变的剪接和复杂性状之间建立直接联系仍然是一个持久的挑战。我们引入了剪接-转录组全关联(SpliTWAS),将替代剪接信息与全基因组关联研究结合起来,通过外显子剪接事件确定与性状相关的基因。我们将 SpliTWAS 应用于两个精神分裂症(SCZ)RNA 序列数据集 BrainGVEX 和 CommonMind,分别发现了 137 和 88 个性状相关外显子(分别位于 84 和 67 个基因中)。相关基因集中丰富的生物功能集中在神经元功能和发育、免疫细胞激活和细胞转运上,这些功能与 SCZ 高度相关。SpliTWAS 变异影响了 RNA 结合蛋白结合位点,揭示了影响剪接的 RNA 蛋白相互作用的潜在破坏。我们将概率精细映射方法FOCUS扩展到了外显子水平,确定了36个基因和48个外显子可能与SCZ有因果关系。我们特别强调了VPS45和APOPT1,在这两个基因中,特定外显子的剪接与疾病风险有关,而传统的基因表达分析无法检测到。总之,这项研究证实了替代剪接在形成 SCZ 遗传基础中的重要作用,为这一领域未来的研究提供了宝贵的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Splicing-specific transcriptome-wide association uncovers genetic mechanisms for schizophrenia.

Recent studies have highlighted the essential role of RNA splicing, a key mechanism of alternative RNA processing, in establishing connections between genetic variations and disease. Genetic loci influencing RNA splicing variations show considerable influence on complex traits, possibly surpassing those affecting total gene expression. Dysregulated RNA splicing has emerged as a major potential contributor to neurological and psychiatric disorders, likely due to the exceptionally high prevalence of alternatively spliced genes in the human brain. Nevertheless, establishing direct associations between genetically altered splicing and complex traits has remained an enduring challenge. We introduce Spliced-Transcriptome-Wide Associations (SpliTWAS) to integrate alternative splicing information with genome-wide association studies to pinpoint genes linked to traits through exon splicing events. We applied SpliTWAS to two schizophrenia (SCZ) RNA-sequencing datasets, BrainGVEX and CommonMind, revealing 137 and 88 trait-associated exons (in 84 and 67 genes), respectively. Enriched biological functions in the associated gene sets converged on neuronal function and development, immune cell activation, and cellular transport, which are highly relevant to SCZ. SpliTWAS variants impacted RNA-binding protein binding sites, revealing potential disruption of RNA-protein interactions affecting splicing. We extended the probabilistic fine-mapping method FOCUS to the exon level, identifying 36 genes and 48 exons as putatively causal for SCZ. We highlight VPS45 and APOPT1, where splicing of specific exons was associated with disease risk, eluding detection by conventional gene expression analysis. Collectively, this study supports the substantial role of alternative splicing in shaping the genetic basis of SCZ, providing a valuable approach for future investigations in this area.

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来源期刊
CiteScore
14.70
自引率
4.10%
发文量
185
审稿时长
1 months
期刊介绍: The American Journal of Human Genetics (AJHG) is a monthly journal published by Cell Press, chosen by The American Society of Human Genetics (ASHG) as its premier publication starting from January 2008. AJHG represents Cell Press's first society-owned journal, and both ASHG and Cell Press anticipate significant synergies between AJHG content and that of other Cell Press titles.
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