生物
多效性
基因
遗传学
全基因组关联研究
遗传关联
遗传建筑学
基因调控网络
计算生物学
候选基因
表型
基因组
疾病
单核苷酸多态性
基因表达
基因型
医学
病理
作者
Inigo Barrio-Hernandez,Jeremy Schwartzentruber,Anjali Shrivastava,Noemi Del-Toro,Asier Gonzalez,Qian Zhang,Edward Mountjoy,Daniel Suveges,David Ochoa,Maya Ghoussaini,Glyn Bradley,Henning Hermjakob,Sandra Orchard,Ian Dunham,Carl A Anderson,Pablo Porras,Pedro Beltrao
出处
期刊:Nature Genetics
[Nature Portfolio]
日期:2023-02-23
卷期号:55 (3): 389-398
被引量:4
标识
DOI:10.1038/s41588-023-01327-9
摘要
Interacting proteins tend to have similar functions, influencing the same organismal traits. Interaction networks can be used to expand the list of candidate trait-associated genes from genome-wide association studies. Here, we performed network-based expansion of trait-associated genes for 1,002 human traits showing that this recovers known disease genes or drug targets. The similarity of network expansion scores identifies groups of traits likely to share an underlying genetic and biological process. We identified 73 pleiotropic gene modules linked to multiple traits, enriched in genes involved in processes such as protein ubiquitination and RNA processing. In contrast to gene deletion studies, pleiotropy as defined here captures specifically multicellular-related processes. We show examples of modules linked to human diseases enriched in genes with known pathogenic variants that can be used to map targets of approved drugs for repurposing. Finally, we illustrate the use of network expansion scores to study genes at inflammatory bowel disease genome-wide association study loci, and implicate inflammatory bowel disease-relevant genes with strong functional and genetic support.
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