Abstract

BackgroundIn aerobically grown cells, iron homeostasis and oxidative stress are tightly linked processes implicated in a growing number of diseases. The deregulation of iron homeostasis due to gene defects or environmental stresses leads to a wide range of diseases with consequences for cellular metabolism that remain poorly understood. The modelling of iron homeostasis in relation to the main features of metabolism, energy production and oxidative stress may provide new clues to the ways in which changes in biological processes in a normal cell lead to disease.ResultsUsing a methodology based on probabilistic Boolean modelling, we constructed the first model of yeast iron homeostasis including oxygen-related reactions in the frame of central metabolism. The resulting model of 642 elements and 1007 reactions was validated by comparing simulations with a large body of experimental results (147 phenotypes and 11 metabolic flux experiments). We removed every gene, thus generating in silico mutants. The simulations of the different mutants gave rise to a remarkably accurate qualitative description of most of the experimental phenotype (overall consistency > 91.5%). A second validation involved analysing the anaerobiosis to aerobiosis transition. Therefore, we compared the simulations of our model with different levels of oxygen to experimental metabolic flux data. The simulations reproducted accurately ten out of the eleven metabolic fluxes. We show here that our probabilistic Boolean modelling strategy provides a useful description of the dynamics of a complex biological system. A clustering analysis of the simulations of all in silico mutations led to the identification of clear phenotypic profiles, thus providing new insights into some metabolic response to stress conditions. Finally, the model was also used to explore several new hypothesis in order to better understand some unexpected phenotypes in given mutants.ConclusionsAll these results show that this model, and the underlying modelling strategy, are powerful tools for improving our understanding of complex biological problems.

Highlights

  • In aerobically grown cells, iron homeostasis and oxidative stress are tightly linked processes implicated in a growing number of diseases

  • We focused on iron homeostasis and oxidative stress

  • Any model developed to analyse the relationship between iron homeostasis and oxidative stress damage must be able to deal with several different levels of knowledge about a large number of elements and reactions

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Summary

Introduction

Iron homeostasis and oxidative stress are tightly linked processes implicated in a growing number of diseases. The deregulation of iron homeostasis due to gene defects or environmental stresses leads to a wide range of diseases with consequences for cellular metabolism that remain poorly understood. Due to its unique redox properties and chemical reactivity, iron appears to be a key player in abnormal ROS generation, principally as a catalyst of the Fenton and Haber-Weiss reactions [12] This essential micronutrient is the redox component of the haem and iron-sulphur cluster [FeS] cofactors of many important proteins or enzymes. The deregulation of iron homeostasis due to gene defects or environmental stresses leads to a wide range of diseases, from anaemia (iron deficiency) to haemochromatosis (iron overload) [13,14,15] with consequences for cellular metabolism that remain poorly understood. The modelling of iron homeostasis in relation to the main features of metabolism, energy production and oxidative stress may provide new clues to the ways in which changes in biological processes in a normal cell lead to disease

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