Abstract

BackgroundResearchers often measure changes in gene expression across conditions to better understand the shared functional roles and regulatory mechanisms of different genes. Analogous to this is comparing gene expression across species, which can improve our understanding of the evolutionary processes shaping the evolution of both individual genes and functional pathways. One area of interest is determining genes showing signals of coevolution, which can also indicate potential functional similarity, analogous to co-expression analysis often performed across conditions for a single species. However, as with any trait, comparing gene expression across species can be confounded by the non-independence of species due to shared ancestry, making standard hypothesis testing inappropriate.ResultsWe compared RNA-Seq data across 18 fungal species using a multivariate Brownian Motion phylogenetic comparative method (PCM), which allowed us to quantify coevolution between protein pairs while directly accounting for the shared ancestry of the species. Our work indicates proteins which physically-interact show stronger signals of coevolution than randomly-generated pairs. Interactions with stronger empirical and computational evidence also showing stronger signals of coevolution. We examined the effects of number of protein interactions and gene expression levels on coevolution, finding both factors are overall poor predictors of the strength of coevolution between a protein pair. Simulations further demonstrate the potential issues of analyzing gene expression coevolution without accounting for shared ancestry in a standard hypothesis testing framework. Furthermore, our simulations indicate the use of a randomly-generated null distribution as a means of determining statistical significance for detecting coevolving genes with phylogenetically-uncorrected correlations, as has previously been done, is less accurate than PCMs, although is a significant improvement over standard hypothesis testing. These methods are further improved by using a phylogenetically-corrected correlation metric.ConclusionsOur work highlights potential benefits of using PCMs to detect gene expression coevolution from high-throughput omics scale data. This framework can be built upon to investigate other evolutionary hypotheses, such as changes in transcription regulatory mechanisms across species.

Highlights

  • Researchers often measure changes in gene expression across conditions to better understand the shared functional roles and regulatory mechanisms of different genes

  • The Candida species appear to be exceptions, but these yeast demonstrate pathogenic traits, which could partially explain some of these differences, as well as why two of these species (C. glabrata and C. parapsilosis) appear to be better correlated with the pathogenic Aspergillus species

  • After filtering proteins based on missing data or violation of the Brownian Motion assumption, our binding and control datasets contained 3,091 and 13,936 protein pairs respectively, consisting of 648 unique proteins

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Summary

Introduction

Researchers often measure changes in gene expression across conditions to better understand the shared functional roles and regulatory mechanisms of different genes. Analogous to this is comparing gene expression across species, which can improve our understanding of the evolutionary processes shaping the evolution of both individual genes and functional pathways. In S. cerevisiae, there is significant overlap between the proteins which physically interact and the proteins which are co-expressed [6] Such observations have naturally led researchers to ask if functionally-related genes show coordinated changes in expression across conditions, do they show coordinated changes, or coevolve, across species. Fraser et al [8] proposed gene expression coevolution could be a useful method for predicting proteins which are functionally-related

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