Abstract

It is widely accepted that cellular requirements and environmental conditions dictate the architecture of genetic regulatory networks. Nonetheless, the status quo in regulatory network modeling and analysis assumes an invariant network topology over time. In this paper, we refocus on a dynamic perspective of genetic networks, one that can uncover substantial topological changes in network structure during biological processes such as developmental growth. We propose a novel outlook on the inference of time-varying genetic networks, from a limited number of noisy observations, by formulating the network estimation as a target tracking problem. We overcome the limited number of observations (small n large p problem) by performing tracking in a compressed domain. Assuming linear dynamics, we derive the LASSO-Kalman smoother, which recursively computes the minimum mean-square sparse estimate of the network connectivity at each time point. The LASSO operator, motivated by the sparsity of the genetic regulatory networks, allows simultaneous signal recovery and compression, thereby reducing the amount of required observations. The smoothing improves the estimation by incorporating all observations. We track the time-varying networks during the life cycle of the Drosophila melanogaster. The recovered networks show that few genes are permanent, whereas most are transient, acting only during specific developmental phases of the organism.

Highlights

  • 1.1 Motivation A major challenge in systems biology today is to understand the behaviors of living cells from the dynamics of complex genomic regulatory networks

  • Assuming linear dynamics of gene expressions, we further show that the model can be decomposed into p independent linear models, p being the number of genes

  • The dynamic view of genetic regulatory networks reveals the temporal information about the onset and duration of genetic interactions, in particular showing that few genes are permanent players in the cellular function while others act transiently during certain phases or ‘regimes’ of the biological process

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Summary

Introduction

1.1 Motivation A major challenge in systems biology today is to understand the behaviors of living cells from the dynamics of complex genomic regulatory networks. The main problem with the segmentation approach for estimating time-varying gene networks is the limited number of time points available in each stationary segment, which is a subset of the already limited data. Full resolution techniques, which allow a time-specific network topology to be inferred from samples measured over the entire time series, rely on model-based approaches [26,27] These methods learn the structure (or skeleton) of the network, but not the detailed strength of the interactions between the nodes. 1.3 Proposed work and contributions In this paper, we propose a novel formulation of the inference of time-varying genomic regulatory networks as a tracking problem, where the target is a set of incoming edges for a given gene. Genomic regulatory networks are known to be sparse: each gene is governed by only a small number of the genes in the network [11]

The LASSO-Kalman smoother
Results and discussion
Time-varying gene networks in Drosophila melanogaster
Conclusions
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