Abstract

Gene interactions in cells can be represented by gene regulatory networks. A Boolean network models gene interactions according to rules where gene expression is represented by binary values (on / off or {1, 0}). In reality, however, the gene’s state can have multiple values due to biological properties. Furthermore, the noisy nature of the experimental design results in uncertainty about a state of the gene. Here we present a new Boolean network paradigm to allow intermediate values on the interval [0, 1]. As in the Boolean network, fixed points or attractors of such a model correspond to biological phenotypes or states. We use our new extension of the Boolean network paradigm to model gene expression in first and second heart field lineages which are cardiac progenitor cell populations involved in early vertebrate heart development. By this we are able to predict additional biological phenotypes that the Boolean model alone is not able to identify without utilizing additional biological knowledge. The additional phenotypes predicted by the model were confirmed by published biological experiments. Furthermore, the new method predicts gene expression propensities for modelled but yet to be analyzed genes.

Highlights

  • Specialization of cells during development and differentiation is driven by transcription or growth factors

  • The gene expression values corresponding to these two fixed points are similar to the gene expression in the FHF and second heart field (SHF) that was extracted from literature

  • In 49% of the initial values, the network converges to attractors corresponding to the FHF (49% of cases) and in 50% to the SHF

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Summary

Introduction

Specialization of cells during development and differentiation is driven by transcription or growth factors. These are interconnected in gene regulatory networks. The temporary regulated interaction of these factors are resulting in terminally differentiated, specialized cells which are characterized by the expression of a certain set of genes. Development and function of a certain cell type is largely reflected by the expression of selected genes in a cell. Gene regulatory networks describe the interactions between those genes in the cell [1,2,3] During embryonic development, these gene regulatory networks evolve over time towards a stable state, reflecting the terminally differentiated cell [1], i.e., biological phenotypes

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