Statistical Epistasis Is a Generic Feature of Gene Regulatory Networks

Arne B. Gjuvsland, Ben J. Hayes, Stig W. Omholt, Örjan Carlborg

Genetics · 2006 · 114 citations · 41 references

DOIFull text

Open access

Concepts

TL;DR

Functional dependencies between genes define gene networks underlying quantitative traits, yet the proportion of genetic variation attributable to statistical epistasis varies widely across studies. The study aims to determine whether distinct functional dependency patterns among polymorphic genes produce different statistical interaction patterns, and to show how combining statistical genetics with nonlinear dynamics can uncover biological insights. We combine a quantitative genetic model with genotype‑phenotype models that translate allelic variation and regulatory principles into gene‑expression phenotypes, integrating statistical genetics with nonlinear system dynamics. Gene regulatory networks with or without feedback motifs can produce diverse statistical genetic architectures, with positive feedback generating higher amounts and more types of epistasis; these findings suggest that including interaction terms in genetic models increases the detection of additional QTL and functional dependencies across regulatory regimes.

Abstract

Functional dependencies between genes are a defining characteristic of gene networks underlying quantitative traits. However, recent studies show that the proportion of the genetic variation that can be attributed to statistical epistasis varies from almost zero to very high. It is thus of fundamental as well as instrumental importance to better understand whether different functional dependency patterns among polymorphic genes give rise to distinct statistical interaction patterns or not. Here we address this issue by combining a quantitative genetic model approach with genotype-phenotype models capable of translating allelic variation and regulatory principles into phenotypic variation at the level of gene expression. We show that gene regulatory networks with and without feedback motifs can exhibit a wide range of possible statistical genetic architectures with regard to both type of effect explaining phenotypic variance and number of apparent loci underlying the observed phenotypic effect. Although all motifs are capable of harboring significant interactions, positive feedback gives rise to higher amounts and more types of statistical epistasis. The results also suggest that the inclusion of statistical interaction terms in genetic models will increase the chance to detect additional QTL as well as functional dependencies between genetic loci over a broad range of regulatory regimes. This article illustrates how statistical genetic methods can fruitfully be combined with nonlinear systems dynamics to elucidate biological issues beyond reach of each methodology in isolation.

References

41