Abstract

MotivationHistone proteins are subject to various posttranslational modifications (PTMs). Elucidating their functional relationships is crucial toward understanding many biological processes. Bayesian network (BN)-based approaches have shown the advantage of revealing causal relationships, rather than simple cooccurrences, of PTMs. Previous works employing BNs to infer causal relationships of PTMs require that all confounders should be included. This assumption, however, is unavoidably violated given the fact that several modifications are often regulated by a common but unobserved factor. An existing non-parametric method can be applied to tackle the problem but the complexity and inflexibility make it impractical.ResultsWe propose a novel BN-based method to infer causal relationships of histone modifications. First, from the evidence that nucleosome organization in vivo significantly affects the activities of PTM regulators working on chromatin substrate, hidden confounders of PTMs are selectively introduced by an information-theoretic criterion. Causal relationships are then inferred from a network model of both PTMs and the derived confounders. Application on human epigenomic data shows the advantage of the proposed method, in terms of computational performance and support from literature. Requiring less strict data assumptions also makes it more practical. Interestingly, analysis of the most significant relationships suggests that the proposed method can recover biologically relevant causal effects between histone modifications, which should be important for future investigation of histone crosstalk.

Highlights

  • Genomes of higher organisms are organized into chromatin, a condensed structure of nucleosome units

  • From the evidence that nucleosome organization in vivo significantly affects the activities of posttranslational modifications (PTMs) regulators working on chromatin substrate, hidden confounders of PTMs are selectively introduced by an information-theoretic criterion

  • PTM profiles were permuted 1000 times and the distributions of the new Mutual information (MI) and Mutual Information Gain (MIG) values for all pair of PTMs were computed for each permutation

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Summary

Introduction

Genomes of higher organisms are organized into chromatin, a condensed structure of nucleosome units. Advances in profiling techniques, such as ChIP-Chip and ChIP-Seq, have enabled the availability of genomescale PTM data [8,9], providing an unprecedented opportunity to decipher histone codes and their associated cis-regulatory elements. It poses a great requirement for methods to understand such data. BN-based approaches may help discover the cooccurrence and the causal relationships of histone modifications [15] This is especially important to understand histone crosstalk, a phenomenon that often occurs among different PTM events [16,17,18]

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