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通过将转录因子相关的易位变异整合到全转录组关联分析中来增强疾病风险基因的发现。

Enhancing Disease Risk Gene Discovery by Integrating Transcription Factor-Linked Trans-located Variants into Transcriptome-Wide Association Analyses.

作者信息

He Jingni, Perera Deshan, Wen Wanqing, Ping Jie, Li Qing, Lyu Linshuoshuo, Chen Zhishan, Shu Xiang, Long Jirong, Cai Qiuyin, Shu Xiao-Ou, Zheng Wei, Long Quan, Guo Xingyi

出版信息

medRxiv. 2024 Jul 7:2023.10.10.23295443. doi: 10.1101/2023.10.10.23295443.

Abstract

Transcriptome-wide association studies (TWAS) have been successful in identifying disease susceptibility genes by integrating cis-variants predicted gene expression with genome-wide association studies (GWAS) data. However, trans-located variants for predicting gene expression remain largely unexplored. Here, we introduce transTF-TWAS, which incorporates transcription factor (TF)-linked trans-located variants to enhance model building. Using data from the Genotype-Tissue Expression project, we predict gene expression and alternative splicing and applied these models to large GWAS datasets for breast, prostate, and lung cancers. We demonstrate that transTF-TWAS outperforms other existing TWAS approaches in both constructing gene prediction models and identifying disease-associated genes, as evidenced by simulations and real data analysis. Our transTF-TWAS approach significantly contributes to the discovery of disease risk genes. Findings from this study have shed new light on several genetically driven key regulators and their associated regulatory networks underlying disease susceptibility.

摘要

全转录组关联研究(TWAS)通过将预测基因表达的顺式变异与全基因组关联研究(GWAS)数据相结合,成功地鉴定出了疾病易感基因。然而,用于预测基因表达的反式定位变异在很大程度上仍未得到充分探索。在此,我们介绍了transTF-TWAS,它整合了与转录因子(TF)相关的反式定位变异以增强模型构建。利用基因型-组织表达项目的数据,我们预测基因表达和可变剪接,并将这些模型应用于乳腺癌、前列腺癌和肺癌的大型GWAS数据集。我们证明,无论是在构建基因预测模型还是在识别疾病相关基因方面,transTF-TWAS都优于其他现有的TWAS方法,模拟和实际数据分析均证明了这一点。我们的transTF-TWAS方法对疾病风险基因的发现做出了重大贡献。这项研究的结果为疾病易感性背后的几个由基因驱动的关键调节因子及其相关调控网络提供了新的线索。

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