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Early life replicators likely emerged through self-priming amplification. This study shows how specific sequences, particularly those favoring purine insertion, dominated in early replication competition, outcompeting less efficient variants.

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Area of Science:

  • Origin of life studies
  • Molecular evolution
  • Biochemistry

Background:

  • Oligonucleotide amplification can occur via self-priming and concatemerization.
  • Phosphorothioate linkages facilitate these processes.
  • Understanding early replicator competition is key to origin of life research.

Purpose of the Study:

  • To investigate the competitive dynamics of early replicators.
  • To identify sequence features that confer a selective advantage during replication.
  • To model potential mechanisms for the emergence of life.

Main Methods:

  • Selection experiments using a library of phosphorothiolated hairpins with random sequences (N10).
  • Inclusion of deoxynucleoside triphosphates and polymerase for amplification.
  • Serial transfer of amplified products to enrich for dominant sequences.

Main Results:

  • Rapid formation of concatemers was observed.
  • Sequences templating purine insertion, especially during initiation, predominated.
  • Specific sequences accumulated over serial transfers, demonstrating competitive advantage.

Conclusions:

  • Self-priming amplification is a viable mechanism for early replicator accumulation.
  • Sequence-dependent templating, particularly purine preference, drove early replicator competition.
  • This mechanism provides insight into how specific replicators may have emerged and persisted near the origin of life.