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Non-Enzymatic Assembly of a Minimized RNA Polymerase Ribozyme
Falk Wachowius1, Philipp Holliger1
1Medical Research Council Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge, CB2 0QH (UK).
Chemsystemschem
|November 2, 2019
Summary
This study shows how complex RNA molecules, essential for the origin of life, can rapidly assemble from simpler activated RNA fragments. This supports a pathway from chemical RNA replication to enzymatic RNA replication.
Area of Science:
- Origin of Life Studies
- Biochemistry
- Molecular Evolution
Background:
- The "RNA world" hypothesis posits RNA catalysts preceded DNA and proteins.
- RNA replicase ribozymes are complex; simpler non-enzymatic RNA replication likely came first.
- Templated polymerization of activated ribonucleotides offers a route to RNA pools for replicase emergence.
Purpose of the Study:
- To demonstrate the rapid assembly of complex ribozymes from activated RNA fragment pools.
- To investigate the transition from non-enzymatic to enzymatic RNA replication.
- To support the RNA world hypothesis by showing feasible RNA self-assembly.
Main Methods:
- Selection and characterization of a minimal RNA polymerase ribozyme variant (150 nucleotides).
- RNA-templated ligation of 5 egular-2-methylimidazole-activated RNA oligomers (less than 30 nucleotides).
- Utilizing phosphorimidazolide (Imp)-activated ribonucleotides for polymerization and replication.
Main Results:
- Successful rapid assembly of complex ribozymes from Imp-activated RNA fragment pools.
- Demonstrated RNA-templated ligation of short activated RNA oligomers to form a functional ribozyme.
- Generated short RNA oligomer pools capable of replication.
Conclusions:
- Complex RNA structures can emerge from pools of activated RNA oligomers.
- Provides a plausible pathway from non-enzymatic/chemical to enzymatic RNA replication.
- Supports the feasibility of RNA self-assembly in early life scenarios.
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