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Updated: May 24, 2026

In Vivo Modeling of the Morbid Human Genome using Danio rerio
Published on: August 24, 2013
A simple model captures key characteristics of biological non-deterministic genotype-phenotype maps
1CRG (Barcelona Collaboratorium for Modelling and Predictive Biology), Barcelona, Spain.
None:
By connecting genotypic mutations to the higher-level phenotypes relevant for selection, genotype-phenotype (GP) maps play a key role in evolution. GP maps are typically investigated using computational models of biophysical phenotypes (for example, RNA secondary structures and simplified models of protein tertiary and quaternary structures), but GP map concepts are relevant beyond these specific models. While there has been significant progress in quantifying GP map properties and their evolutionary implications, this is largely limited to the simplest case, where each genotype corresponds to a single, categorical phenotype. Here, I turn to a more realistic, but also more complex, non-deterministic (ND) treatment, meaning that each genotype generates an ensemble of phenotypes. To provide a tool for tackling the additional complexity of ND GP maps, this paper identifies a tuneable synthetic model that produces an ND GP map reproducing central features of biophysical ND GP maps: phenotypic bias, genetic correlations, a tradeoff between genotypic robustness and evolvability and a non-negative trend between phenotypic robustness and evolvability. These features are reproduced for several alternative models combining additive genotype dependencies with non-linearities, suggesting that few ingredients are needed for these shared features to appear. Moreover, the synthetic ND GP map may be useful as a conceptually and computationally simpler model for addressing open questions about ND GP maps: for simulations linking GP map properties to evolutionary implications, for the development of sampling methods for ND GP maps and for extrapolations.
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