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UTMOST,一项单组织和跨组织的 TWAS(转录组广泛关联研究),揭示了新的与 ASD(自闭症谱系障碍)相关的基因。

UTMOST, a single and cross-tissue TWAS (Transcriptome Wide Association Study), reveals new ASD (Autism Spectrum Disorder) associated genes.

机构信息

Grupo de Medicina Xenómica, Center for Research in Molecular Medicine and Chronic Diseases (CiMUS), Universidad de Santiago de Compostela, Santiago de Compostela, Spain.

Fundación Pública Galega de Medicina Xenómica (FPGMX), Centro de Investigación Biomédica en Red, Enfermedades Raras (CIBERER), Universidad de Santiago de Compostela, Santiago de Compostela, Spain.

出版信息

Transl Psychiatry. 2021 Apr 30;11(1):256. doi: 10.1038/s41398-021-01378-8.

Abstract

Autism spectrum disorders (ASD) is a complex neurodevelopmental disorder that may significantly impact on the affected individual's life. Common variation (SNPs) could explain about 50% of ASD heritability. Despite this fact and the large size of the last GWAS meta-analysis, it is believed that hundreds of risk genes in ASD have yet to be discovered. New tools, such as TWAS (Transcriptome Wide Association Studies) which integrate tissue expression and genetic data, are a great approach to identify new ASD susceptibility genes. The main goal of this study is to use UTMOST with the publicly available summary statistics from the largest ASD GWAS meta-analysis as genetic input. In addition, an in silico biological characterization for the novel associated loci was performed. Our results have shown the association of 4 genes at the brain level (CIPC, PINX1, NKX2-2, and PTPRE) and have highlighted the association of NKX2-2, MANBA, ERI1, and MITF at the gastrointestinal level. The gastrointestinal associations are quite relevant given the well-established but unexplored relationship between ASD and gastrointestinal symptoms. Cross-tissue analysis has shown the association of NKX2-2 and BLK. UTMOST-associated genes together with their in silico biological characterization seems to point to different biological mechanisms underlying ASD etiology. Thus, it would not be restricted to brain tissue and it will involve the participation of other body tissues such as the gastrointestinal.

摘要

自闭症谱系障碍(ASD)是一种复杂的神经发育障碍,可能会对患者的生活产生重大影响。常见变异(SNP)可以解释大约 50%的 ASD 遗传率。尽管如此,而且之前的 GWAS 荟萃分析规模庞大,但人们相信,还有数百个 ASD 的风险基因尚未被发现。TWAS(转录组广泛关联研究)等新工具,将组织表达和遗传数据相结合,是识别新的 ASD 易感基因的绝佳方法。本研究的主要目标是使用 UTMOST 以及最大的 ASD GWAS 荟萃分析的公开汇总统计数据作为遗传输入。此外,还对新关联的基因座进行了计算机生物学特征分析。我们的研究结果表明,在大脑水平上有 4 个基因(CIPC、PINX1、NKX2-2 和 PTPRE)与 ASD 相关,在胃肠道水平上有 NKX2-2、MANBA、ERI1 和 MITF 与 ASD 相关。鉴于 ASD 与胃肠道症状之间已经建立但尚未得到探索的关系,胃肠道相关性非常重要。跨组织分析表明,NKX2-2 与 BLK 相关。UTMOST 相关基因及其计算机生物学特征分析似乎表明,ASD 病因的生物学机制不同。因此,它不仅局限于脑组织,还将涉及其他身体组织的参与,如胃肠道。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e0d7/8087708/40af0254fa79/41398_2021_1378_Fig1_HTML.jpg

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