Fig. 4From: An interplay of resource availability, population size and mutation rate potentiates the evolution of metabolic signalinga Schematic depiction of key genomic elements from the ancestral organism (top) and representative organisms from H0–H3 peaks obtained from simulations at the high mutation rate (see Fig. 1b). The copy-loop is the first point of difference between these sequences. H0 genotypes have a copy-loop devoid of the ancestral copying functionality. Some of the sample sequences from each of these peaks are given in Additional file 1: Fig. S14. The fitness ranges used to isolate these peaks are given in Additional file 1: Table S2. b Box plots depicting merits (speed of the organism’s virtual CPU, a proxy for metabolic activity of the genotype) of 100 genotypes sampled from each of H0–H3 on the fitness distribution of simulations performed at a high mutation rate (statistical significance measured using the non-parametric Wilcoxon test). c Task complexities for genomes (estimated roughly by the number of “NAND” instructions required to perform a task, increases from left to right) from H0–H3 on the fitness distribution obtained from simulations at high mutation rate. The Y axis represents the number of times that a genotype belonging to these peaks performs a task over a single execution of the genome. Note that peak H3 does not perform any of the metabolic tasks but instead relies on a vastly improved replicative machinery (four h-copy per cycle) to acquire a very high fitness. The data for this figure is also given in Additional file 1: Table S3Back to article page