Before protein enzymes existed, an early genetic polymer would have needed some way to make copies without the sophisticated replication machinery used by modern cells.
Can RNA sequences be copied with sufficient length, speed, and accuracy without modern biological enzymes?
Heredity requires information to be copied. Modern cells accomplish this using highly specialized enzymes and elaborate supporting machinery.
An early RNA-based system could not initially have depended upon those systems because they themselves are products of biological evolution.
Researchers therefore study template-directed nonenzymatic RNA copying. Activated nucleotides can align with complementary bases on an RNA template and under suitable conditions become joined into a new strand.
Without some form of copying, useful molecular sequences disappear when their individual molecules degrade.
Replication makes heredity and cumulative Darwinian evolution possible.
Significant progress has been made in nonenzymatic template-directed RNA copying. Researchers have identified activation chemistries and reaction conditions that improve copying substantially.
Models propose that early RNA replication emerged gradually through chemically driven template copying, perhaps aided by environmental cycles, compartments, catalysts, or subsequently evolved ribozymes.
Challenges include copying long templates, achieving adequate fidelity, copying difficult sequences, separating complementary strands, supplying activated monomers, and repeating the replication cycle.
Replication must preserve enough sequence information for heredity while still allowing variation upon which selection can act.
This is one of the most important experimental tests of natural origin-of-life scenarios.
Intelligent Design should acknowledge genuine progress while asking whether the entire replication cycle can arise and operate under realistically compatible prebiotic conditions.
Important steps in nonenzymatic RNA copying have been demonstrated experimentally. A complete autonomous prebiotic RNA replication system remains an active research goal.