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Computational modeling of anthocyanin pathway evolution: Biases, hotspots, and trade-offs

View ORCID ProfileLucas C. Wheeler, Stacey D. Smith
doi: https://doi.org/10.1101/511089
Lucas C. Wheeler
1Department of Ecology and Evolutionary Biology, University of Colorado, Boulder, CO, USA
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Stacey D. Smith
1Department of Ecology and Evolutionary Biology, University of Colorado, Boulder, CO, USA
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Abstract

Alteration of metabolic pathways is a common mechanism underlying the evolution of new phenotypes. Flower color is a striking example of the importance of metabolic evolution in a complex phenotype, wherein shifts in the activity of the underlying pathway lead to a wide range of pigments. Although experimental work has identified common classes of mutations responsible for transitions among colors, we lack a unifying model that relates pathway function and activity to the evolution of distinct pigment phenotypes. One challenge in creating such a model is the branching structure of pigment pathways, which may lead to evolutionary trade-offs due to competition for shared substrates. In order to predict the effects of shifts in enzyme function and activity on pigment production, we created a simple kinetic model of a major plant pigmentation pathway: the anthocyanin pathway. This model describes the production of the three classes of blue, purple and red anthocyanin pigments, and accordingly, includes multiple branches and substrate competition. We first studied the general behavior of this model using a realistic, functional set of parameters. We then stochastically evolved the pathway toward a defined optimum and analyzed the patterns of fixed mutations. This approach allowed us to quantify the probability density of trajectories through pathway state space and identify the types and number of changes. Finally, we examined whether the observed trajectories and constraints align with experimental observations, i.e., the predominance of mutations which change color by altering the function of branching genes in the pathway. These analyses provide a theoretical framework that can be used to predict the consequences of new mutations in terms of both pigment phenotypes and pleiotropic effects.

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Posted January 31, 2019.
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Computational modeling of anthocyanin pathway evolution: Biases, hotspots, and trade-offs
Lucas C. Wheeler, Stacey D. Smith
bioRxiv 511089; doi: https://doi.org/10.1101/511089
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Computational modeling of anthocyanin pathway evolution: Biases, hotspots, and trade-offs
Lucas C. Wheeler, Stacey D. Smith
bioRxiv 511089; doi: https://doi.org/10.1101/511089

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