Cooperative ligation breaks sequence symmetry and stabilizes early molecular replication

TL;DR

This study demonstrates that cooperative templated ligation can break sequence symmetry and promote early molecular replication, potentially explaining how life’s first sequences emerged and evolved from prebiotic chemistry.

Contribution

The paper introduces experimental and theoretical evidence that cooperative ligation enables self-selection and nonlinear replication, bridging polymerization and Darwinian evolution in origin-of-life scenarios.

Findings

Cooperative ligation leads to nonlinear sequence amplification.

Thermal cycling facilitates strand reshuffling and replication.

Mechanism may serve as a bridge from prebiotic polymerization to life.

Abstract

Each living species carries a complex DNA sequence that determines their unique features and functionalities. It is generally assumed that life started from a random pool of oligonucleotides sequences, generated by a prebiotic polymerization of nucleotides. The mechanism that initially facilitated the emergence of sequences that code for the function of the first species from such a random pool of sequences remains unknown. It is a central problem of the origin of life. An interesting option would be a self-selection mechanism by spontaneous symmetry breaking. Initial concentration fluctuations of specific sequence motifs would have been amplified and outcompeted less abundant sequences, enhancing the signal to noise to replicate and select functional sequences. Here, we demonstrate with experimental and theoretical findings that templated ligation would provide such a self-selection. In templated ligation, two adjacent single sequences strands are chemically joined when a third complementary strand sequence brought them in close proximity. This simple mechanism was a likely side-product of a prebiotic polymerization chemistry once the strands reach the length to form double stranded species. As shown here, the ligation gave rise to a nonlinear replication process by the cooperative ligation of matching sequences which self-promoted their own elongation. This led to a cascade of enhanced template binding and faster ligation reactions. A requirement was the reshuffling of the strands by thermal cycling, enabled for example by microscale convection. Assuming that templated ligation was driven by the same chemical mechanism that generated prebiotic polymerization of oligonucleotides, the mechanism could function as a missing link between polymerization and the self-stabilized replication, offering a pathway to the autonomous emergence of Darwinian evolution for the origin of life.