A model of gene expression based on random dynamical systems reveals modularity properties of gene regulatory networks.

Math Biosci

Departamento de Microbiologia, Imunologia e Parasitologia, Escola Paulista de Medicina (EPM), Universidade Federal de São Paulo (UNIFESP), SP, Brasil; Laboratório de Genômica Evolutiva e Biocomplexidade, EPM, UNIFESP, Ed. Pesquisas II, Rua Pedro de Toledo 669, CEP 04039-032, São Paulo, Brasil.

Published: June 2016

AI Article Synopsis

  • This text proposes a new method for modeling gene expression using random dynamical systems (RDS), highlighting its ability to couple regulatory network nodes while maintaining modularity.
  • The approach allows for large-scale networks through simple components, utilizes general assumptions about stochastic processes, and employs a well-established mathematical framework to analyze system dynamics without solving equations directly.
  • Additionally, it emphasizes that coupling RDS is complex and provides assurances that their coupling method produces valid regulatory networks, with classical rate equations serving as a reliable foundation for validation and prediction.

Article Abstract

Here we propose a new approach to modeling gene expression based on the theory of random dynamical systems (RDS) that provides a general coupling prescription between the nodes of any given regulatory network given the dynamics of each node is modeled by a RDS. The main virtues of this approach are the following: (i) it provides a natural way to obtain arbitrarily large networks by coupling together simple basic pieces, thus revealing the modularity of regulatory networks; (ii) the assumptions about the stochastic processes used in the modeling are fairly general, in the sense that the only requirement is stationarity; (iii) there is a well developed mathematical theory, which is a blend of smooth dynamical systems theory, ergodic theory and stochastic analysis that allows one to extract relevant dynamical and statistical information without solving the system; (iv) one may obtain the classical rate equations form the corresponding stochastic version by averaging the dynamic random variables (small noise limit). It is important to emphasize that unlike the deterministic case, where coupling two equations is a trivial matter, coupling two RDS is non-trivial, specially in our case, where the coupling is performed between a state variable of one gene and the switching stochastic process of another gene and, hence, it is not a priori true that the resulting coupled system will satisfy the definition of a random dynamical system. We shall provide the necessary arguments that ensure that our coupling prescription does indeed furnish a coupled regulatory network of random dynamical systems. Finally, the fact that classical rate equations are the small noise limit of our stochastic model ensures that any validation or prediction made on the basis of the classical theory is also a validation or prediction of our model. We illustrate our framework with some simple examples of single-gene system and network motifs.

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http://dx.doi.org/10.1016/j.mbs.2016.03.008DOI Listing

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