Abstract

Expression quantitative trait loci (eQTL) studies have generated large amounts of data in different organisms. The analyses of these data have led to many novel findings and biological insights on expression regulations. However, the role of epistasis in the joint regulation of multiple genes has not been explored. This is largely due to the computational complexity involved when multiple traits are simultaneously considered against multiple markers if an exhaustive search strategy is adopted. In this article, we propose a computationally feasible approach to identify pairs of chromosomal regions that interact to regulate co-expression patterns of pairs of genes. Our approach is built on a bivariate model whose covariance matrix depends on the joint genotypes at the candidate loci. We also propose a filtering process to reduce the computational burden. When we applied our method to a yeast eQTL dataset profiled under both the glucose and ethanol conditions, we identified a total of 225 and 224 modules, with each module consisting of two genes and two eQTLs where the two eQTLs epistatically regulate the co-expression patterns of the two genes. We found that many of these modules have biological interpretations. Under the glucose condition, ribosome biogenesis was co-regulated with the signaling and carbohydrate catabolic processes, whereas silencing and aging related genes were co-regulated under the ethanol condition with the eQTLs containing genes involved in oxidative stress response process.

Highlights

  • EQTL studies aim to uncover the genetic architecture underlying expression regulation

  • To understand how environmental conditions modulate the effects of genetic variants on phenotypic traits, we investigated whether the gene pairs in the inferred Epistasis-2D modules are enriched for certain biological processes

  • We have developed a novel statistical approach to identifying gene pairs whose co-expression patterns are jointly regulated by interacting loci through the analysis of Expression quantitative trait loci (eQTL) data

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Summary

Introduction

EQTL studies aim to uncover the genetic architecture underlying expression regulation. Storey et al [8] developed a stepwise regression method to detect epistasis on the genome-wide scale This method is computationally feasible but may miss epistatic effects involving markers having weak marginal effects. To reduce the model search space and increase statistical power, Lee et al adopted genetic interaction networks identified by large-scale synthetic genetic array (SGA) analysis as prior for detecting epistasis in yeast [11]. Since they only consider interacting SNPs that have already been identified, its application is limited to those organisms where comprehensive prior knowledge is available, which is rare in practice

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