See MMathPhys oral presentation
–The structure of the genotype–phenotype map strongly constrains the evolution of non-coding RNA. See notes
Probabilistic bias in genotype-phenotype maps. See more here: http://dingleresearch.weebly.com/publications.html
Self-assembling polyominoes model: A tractable genotype–phenotype map modelling the self-assembly of protein quaternary structure
More.... Modeling the evolution of molecular systems from a mechanistic perspective Adaptive dynamics under development-based genotype–phenotype maps Why self-incompatibility in the Brassicaceae is totally cool
3. The organization of biological sequences into constrained and unconstrained parts determines fundamental properties of genotype–phenotype maps. Features observed in several GP maps (including the simple Fibonacci GP map they use as a model):
random null model: that maintains the number of genotypes mapping to each phenotype, but assigns genotypes randomly
Genetic correlations
neutral correlations can be quantified by the robustness to mutations, which can be many orders of magnitude larger than that of the null model, and crucially, above the critical threshold for the formation of large neutral networks of mutationally connected genotypes which enhance the capacity for the exploration of phenotypic novelty. Thus neutral correlations increase evolvability.
non-neutral correlations: Compared to the null model:
Non-neutral correlations of type i) and ii) reduce the rate at which new phenotypes can be found by neutral exploration, and so may diminish evolvability, while non-neutral correlations of type iii) may instead facilitate evolutionary exploration and so increase evolvability.
suggesting that some of the results discussed in this paper for RNA may hold more widely in biology
See also Evolving automata
Paper with several examples of GP maps, including cellular automata map: An investigation of redundant genotype-phenotype mappings and their role in evolutionary search