Abstract

The inference of gene regulatory networks (GRNs) from expression data is a challenging problem in systems biology. The stochasticity or fluctuations in the biochemical processes that regulate the transcription process poses as one of the major challenges. In this paper, we propose a novel GRN inference approach, named the Probabilistic Extended Petri Net for Gene Regulatory Network (PEPN-GRN), for the inference of gene regulatory networks from noisy expression data. The proposed inference approach makes use of transition of discrete gene expression levels across adjacent time points as different evidence types that relate to the production or decay of genes. The paper examines three variants of the PEPN-GRN method, which mainly differ by the way the scores of network edges are computed using evidence types. The proposed method is evaluated on the benchmark DREAM4 in silico data sets and a real time series data set of E. coli from the DREAM5 challenge. The PEPN-GRN_v3 variant (the third variant of the PEPN-GRN approach) sought to learn the weights of evidence types in accordance with their contribution to the activation and inhibition gene regulation process. The learned weights help understand the time-shifted and inverted time-shifted relationship between regulator and target gene. Thus, PEPN-GRN_v3, along with the inference of network edges, also provides a functional understanding of the gene regulation process.

Highlights

  • There are different kinds of processes in the cell that work together to perform different activities

  • We proposed a probabilistic inference approach, PEPN-GRN for gene regulatory networks from noisy expression data sets

  • The paper presents three variants of the proposed PEPN-GRN inference approach which differ mainly by the way the different evidence probabilities for an inferred edge are aggregated for score computation

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Summary

Introduction

There are different kinds of processes in the cell that work together to perform different activities. Depending upon the components and their interaction types, at large, we have three kinds of biochemical networks at the sub-cellular level: metabolic networks, signal transduction networks, and gene regulatory networks. A gene regulatory network (GRN) is a network of genegene interactions that govern their expression. Regulation of gene expression is important as it regulates the amount of protein production in the cell. Inference of gene regulatory networks is considered as one of the key problems in Systems Biology [1, 2]. There has been an exponential growth of reverse engineering methods for network reconstruction over the last two decades [3,4,5,6,7].

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