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Multimodal Analysis of RNA Sequencing Data Powers Discovery of Complex Trait Genetics

NATURE COMMUNICATIONS(2024)

Univ Calif San Diego | Scripps Res | Seattle Childrens Res Inst | Dana Farber Canc Inst

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Abstract
RNA sequencing has the potential to reveal many modalities of transcriptional regulation, such as various splicing phenotypes, but studies on gene regulation are often limited to gene expression due to the complexity of extracting and analyzing multiple RNA phenotypes. Here, we present Pantry, a framework to efficiently generate diverse RNA phenotypes from RNA sequencing data and perform downstream integrative analyses with genetic data. Pantry generates phenotypes from six modalities of transcriptional regulation (gene expression, isoform ratios, splice junction usage, alternative TSS/polyA usage, and RNA stability) and integrates them with genetic data via QTL mapping, TWAS, and colocalization testing. We apply Pantry to Geuvadis and GTEx data, finding that 4768 of the genes with no identified eQTL in Geuvadis have QTL in at least one other transcriptional modality, resulting in a 66% increase in genes over eQTL mapping. We further found that the QTL exhibit modality-specific functional properties that are further reinforced by joint analysis of different RNA modalities. We also show that generalizing TWAS to multiple RNA modalities approximately doubles the discovery of unique gene-trait associations, and enhances identification of regulatory mechanisms underlying GWAS signal in 42% of previously associated gene-trait pairs. Here, the authors present the Pantry framework, which extracts features from RNA sequencing data and performs multimodal genetic analyses. This type of analysis can increase gene-trait associations identified compared to using only expression levels.
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要点】:本文提出了Pantry框架,通过从RNA测序数据中提取多种转录调控模态的特征,并与遗传数据整合,增强了复杂性状遗传关联的研究,提高了基因-性状关联的发现数量。

方法】:Pantry框架从六种转录调控模态(基因表达、转录变体比例、剪接位点使用、选择性启动子/多腺苷酸使用和RNA稳定性)生成表型,并通过QTL映射、TWAS和共定位测试与遗传数据整合。

实验】:作者将Pantry应用于Geuvadis和GTEx数据,发现Geuvadis中未识别的eQTL基因中有4768个至少在其他一种转录调控模态中存在QTL,使基因数量增加了66%,并展示了通过多种RNA模态的联合分析可以增强QTL的功能特性识别,以及将TWAS推广到多种RNA模态几乎翻倍地发现了独特的基因-性状关联。