The origin of a primordial genome through spontaneous symmetry breaking

• Published in: Nature communications 2017-08, Vol.8 (1), p.250-11, Article 250
• Main Authors: Takeuchi, Nobuto, Hogeweg, Paulien, Kaneko, Kunihiko
• Format: Article
• Language: English
• Subjects: 631/114/2397; 631/181/2468; 631/181/904; Artificial Cells - chemistry; Asymmetry; Broken symmetry; Catalysis; Catalysts; Copy number; Differentiation; Enzymes; Evolution, Molecular; Genetic Drift; Genome; Genomes; Humanities and Social Sciences; Models, Genetic; multidisciplinary; Replication; Science; Science (multidisciplinary); Strands; Symmetry
• ISSN: 2041-1723; 2041-1723
• DOI: 10.1038/s41467-017-00243-x

The heredity of a cell is provided by a small number of non-catalytic templates—the genome. How did genomes originate? Here, we demonstrate the possibility that genome-like molecules arise from symmetry breaking between complementary strands of self-replicating molecules. Our model assumes a population of protocells, each containing a population of self-replicating catalytic molecules. The protocells evolve towards maximising the catalytic activities of the molecules to increase their growth rates. Conversely, the molecules evolve towards minimising their catalytic activities to increase their intracellular relative fitness. These conflicting tendencies induce the symmetry breaking, whereby one strand of the molecules remains catalytic and increases its copy number (enzyme-like molecules), whereas the other becomes non-catalytic and decreases its copy number (genome-like molecules). This asymmetry increases the equilibrium cellular fitness by decreasing mutation pressure and increasing intracellular genetic drift. These results implicate conflicting multilevel evolution as a key cause of the origin of genetic complexity. Early molecules of life likely served both as templates and catalysts, raising the question of how functionally distinct genomes and enzymes arose. Here, the authors show that conflict between evolution at the molecular and cellular levels can drive functional differentiation of the two strands of self-replicating molecules and lead to copy number differences between the two.