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      A framework for evolutionary systems biology

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      1 ,
      BMC Systems Biology
      BioMed Central

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          Abstract

          Background

          Many difficult problems in evolutionary genomics are related to mutations that have weak effects on fitness, as the consequences of mutations with large effects are often simple to predict. Current systems biology has accumulated much data on mutations with large effects and can predict the properties of knockout mutants in some systems. However experimental methods are too insensitive to observe small effects.

          Results

          Here I propose a novel framework that brings together evolutionary theory and current systems biology approaches in order to quantify small effects of mutations and their epistatic interactions in silico. Central to this approach is the definition of fitness correlates that can be computed in some current systems biology models employing the rigorous algorithms that are at the core of much work in computational systems biology. The framework exploits synergies between the realism of such models and the need to understand real systems in evolutionary theory. This framework can address many longstanding topics in evolutionary biology by defining various 'levels' of the adaptive landscape. Addressed topics include the distribution of mutational effects on fitness, as well as the nature of advantageous mutations, epistasis and robustness. Combining corresponding parameter estimates with population genetics models raises the possibility of testing evolutionary hypotheses at a new level of realism.

          Conclusion

          EvoSysBio is expected to lead to a more detailed understanding of the fundamental principles of life by combining knowledge about well-known biological systems from several disciplines. This will benefit both evolutionary theory and current systems biology. Understanding robustness by analysing distributions of mutational effects and epistasis is pivotal for drug design, cancer research, responsible genetic engineering in synthetic biology and many other practical applications.

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          Most cited references295

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          Stochastic simulation of chemical kinetics.

          Stochastic chemical kinetics describes the time evolution of a well-stirred chemically reacting system in a way that takes into account the fact that molecules come in whole numbers and exhibit some degree of randomness in their dynamical behavior. Researchers are increasingly using this approach to chemical kinetics in the analysis of cellular systems in biology, where the small molecular populations of only a few reactant species can lead to deviations from the predictions of the deterministic differential equations of classical chemical kinetics. After reviewing the supporting theory of stochastic chemical kinetics, I discuss some recent advances in methods for using that theory to make numerical simulations. These include improvements to the exact stochastic simulation algorithm (SSA) and the approximate explicit tau-leaping procedure, as well as the development of two approximate strategies for simulating systems that are dynamically stiff: implicit tau-leaping and the slow-scale SSA.
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            Nothing in Biology Makes Sense except in the Light of Evolution

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              Morphology, Performance and Fitness

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                Author and article information

                Journal
                BMC Syst Biol
                BMC Systems Biology
                BioMed Central
                1752-0509
                2009
                24 February 2009
                : 3
                : 27
                Affiliations
                [1 ]Centre for Systems Biology at Edinburgh, The University of Edinburgh, Darwin building, Kings Buildings, Mayfield Road, Edinburgh, Scotland, EH9 3JU, UK
                Article
                1752-0509-3-27
                10.1186/1752-0509-3-27
                2663779
                19239699
                6f167758-1422-48a1-af0c-f079003f844a
                Copyright © 2009 Loewe; licensee BioMed Central Ltd.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 1 July 2008
                : 24 February 2009
                Categories
                Correspondence

                Quantitative & Systems biology
                Quantitative & Systems biology

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