Marginal interaction test for detecting interactions between genetic marker sets and environment in genome-wide studies.

IF 2.1 3区 生物学 Q3 GENETICS & HEREDITY G3: Genes|Genomes|Genetics Pub Date : 2024-11-14 DOI:10.1093/g3journal/jkae263
Linchuan Shen, Amei Amei, Bowen Liu, Gang Xu, Yunqing Liu, Edwin C Oh, Xin Zhou, Zuoheng Wang
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Abstract

As human complex diseases are influenced by the interaction between genetics and the environment, identifying gene-environment interactions (G × E) is crucial for understanding disease mechanisms and predicting risk. Developing robust quantitative tools for G × E analysis can enhance the study of complex diseases. However, many existing methods that explore G × E focus on the interplay between an environmental factor and genetic variants, exclusively for common or rare variants. In this study, we developed MAGEIT_RAN and MAGEIT_FIX to identify interactions between an environmental factor and a set of genetic markers, including both rare and common variants, based on the MinQue for Summary statistics. The genetic main effects in MAGEIT_RAN and MAGEIT_FIX are modeled as random and fixed effects, respectively. Simulation studies showed that both tests had type I error under control, with MAGEIT_RAN being the most powerful test. Applying MAGEIT to a genome-wide analysis of gene-alcohol interactions on hypertension and seated systolic blood pressure in the Multi-Ethnic Study of Atherosclerosis revealed genes like EIF2AK2, CCNDBP1 and EPB42 influencing blood pressure through alcohol interaction. Pathway analysis identified one apoptosis and survival pathway involving PKR and two signal transduction pathways associated with hypertension and alcohol intake, demonstrating MAGEIT_RAN's ability to detect biologically relevant gene-environment interactions.

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边际交互检验,用于检测全基因组研究中遗传标记集与环境之间的交互作用。
由于人类复杂疾病受遗传和环境之间相互作用的影响,识别基因与环境之间的相互作用(G × E)对于了解疾病机制和预测风险至关重要。为 G × E 分析开发强大的定量工具可以加强对复杂疾病的研究。然而,现有的许多探索 G × E 的方法都侧重于环境因素与遗传变异之间的相互作用,只针对常见或罕见变异。在本研究中,我们开发了 MAGEIT_RAN 和 MAGEIT_FIX,以识别环境因素与一组遗传标记(包括罕见变异和常见变异)之间的相互作用。MAGEIT_RAN 和 MAGEIT_FIX 中的遗传主效应分别建模为随机效应和固定效应。模拟研究表明,这两种检验的 I 型误差都在可控范围内,其中 MAGEIT_RAN 是最强大的检验。应用 MAGEIT 对动脉粥样硬化多种族研究中高血压和坐位收缩压的基因-酒精交互作用进行全基因组分析,发现 EIF2AK2、CCNDBP1 和 EPB42 等基因通过酒精交互作用影响血压。通路分析发现了一条涉及 PKR 的凋亡和存活通路,以及两条与高血压和酒精摄入相关的信号转导通路,证明了 MAGEIT_RAN 检测生物相关基因-环境相互作用的能力。
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来源期刊
G3: Genes|Genomes|Genetics
G3: Genes|Genomes|Genetics GENETICS & HEREDITY-
CiteScore
5.10
自引率
3.80%
发文量
305
审稿时长
3-8 weeks
期刊介绍: G3: Genes, Genomes, Genetics provides a forum for the publication of high‐quality foundational research, particularly research that generates useful genetic and genomic information such as genome maps, single gene studies, genome‐wide association and QTL studies, as well as genome reports, mutant screens, and advances in methods and technology. The Editorial Board of G3 believes that rapid dissemination of these data is the necessary foundation for analysis that leads to mechanistic insights. G3, published by the Genetics Society of America, meets the critical and growing need of the genetics community for rapid review and publication of important results in all areas of genetics. G3 offers the opportunity to publish the puzzling finding or to present unpublished results that may not have been submitted for review and publication due to a perceived lack of a potential high-impact finding. G3 has earned the DOAJ Seal, which is a mark of certification for open access journals, awarded by DOAJ to journals that achieve a high level of openness, adhere to Best Practice and high publishing standards.
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