Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2816745 | Gene | 2014 | 6 Pages |
•Computational modeling is needed to understand complex molecular networks.•We provide guidelines for experimental design and model construction.•The process of modeling can be used to generate new hypotheses.•We studied gene expression and signal transduction in human articular chondrocytes.•WNT and IL-1B pathways seem to display crosstalk at the signal transduction level.
Computational modeling of biological networks permits the comprehensive analysis of cells and tissues to define molecular phenotypes and novel hypotheses. Although a large number of software tools have been developed, the versatility of these tools is limited by mathematical complexities that prevent their broad adoption and effective use by molecular biologists. This study clarifies the basic aspects of molecular modeling, how to convert data into useful input, as well as the number of time points and molecular parameters that should be considered for molecular regulatory models with both explanatory and predictive potential. We illustrate the necessary experimental preconditions for converting data into a computational model of network dynamics. This model requires neither a thorough background in mathematics nor precise data on intracellular concentrations, binding affinities or reaction kinetics. Finally, we show how an interactive model of crosstalk between signal transduction pathways in primary human articular chondrocytes allows insight into processes that regulate gene expression.
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