Are trait‐associated genes clustered together in a gene network?

Abstract

AbstractGenome‐wide association studies (GWAS) have provided an abundance of information about the genetic variants and their loci that are associated to complex traits and diseases. However, due to linkage disequilibrium (LD) and noncoding regions of loci, it remains a challenge to pinpoint the causal genes. Gene network‐based approaches, paired with network diffusion methods, have been proposed to prioritize causal genes and to boost statistical power in GWAS based on the assumption that trait‐associated genes are clustered in a gene network. Due to the difficulty in mapping trait‐associated variants to genes in GWAS, this assumption has never been directly or rigorously tested empirically. On the other hand, whole exome sequencing (WES) data focuses on the protein‐coding regions, directly identifying trait‐associated genes. In this study, we tested the assumption by leveraging the recently available exome‐based association statistics from the UK Biobank WES data along with two types of networks. We found that almost all trait‐associated genes were significantly more proximal to each other than randomly selected genes within both networks. These results support the assumption that trait‐associated genes are clustered in gene networks, which can be further leveraged to boost the power of GWAS such as by introducing less stringent p value thresholds.