Origin & Evolution of Life

RNA World: Overcoming Nucleotide Bias In The Nonenzymatic Copying Of RNA Templates

By Keith Cowing
Status Report
biorxiv.org
September 6, 2024
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RNA World: Overcoming Nucleotide Bias In The Nonenzymatic Copying Of RNA Templates
A hairpin loop from a pre-mRNA. Highlighted are the nucleobases (green) and the ribose-phosphate backbone (blue). — Wikipedia

The RNA World hypothesis posits that RNA was the molecule of both heredity and function during the emergence of life.

This hypothesis implies that RNA templates can be copied, and ultimately replicated, without the catalytic aid of evolved enzymes.

A major problem with nonenzymatic templated polymerization has been the very poor copying of sequences containing rA and rU.

Here we overcome that problem by using a prebiotically plausible mixture of RNA mononucleotides and random-sequence oligonucleotides, all activated by methyl isocyanide chemistry, that direct the uniform copying of arbitrary-sequence templates, including those harboring rA and rU.

We further show that the use of this mixture in copying reactions suppresses copying errors while also generating a more uniform distribution of mismatches than observed for simpler systems.

We find that oligonucleotide competition for template binding sites, oligonucleotide ligation, and the template binding properties of reactant intermediates work together to reduce product sequence bias and errors.

Finally, we show that iterative cycling of the activation chemistry and templated polymerization improves the yield of random-sequence products. These results for random-sequence template copying are a significant advance in the pursuit of nonenzymatic RNA replication.

Templated nonenzymatic polymerization, activation chemistry, and sequencing of products. A. Mechanism of templated polymerization by imidazole-activated 5′-5′ bridged dinucleotide that can bind a primer-template junction. B. Direct extension via the activated mononucleotide. C. A downstream oligonucleotide can sandwich any reactive species against the primer. D. A mononucleotide can form a 5′-5′ bridged species with an oligonucleotide. E. Direct ligation of an activated oligonucleotide, analogous to mechanism (B). F. Ligation via a sterically displaced 5′ bridged mononucleotide. G. Many species compete for binding sites in a heterogeneous reaction. H. A mixture of mono- and oligonucleotides can be activated in situ by MeNC-mediated chemistry. I. (Adapted from 1.) — biorxiv.org

Daniel Duzdevich, Christopher E. Carr, Benjamin Colville, Harry R.M. Aitken,Jack W. Szostak

Overcoming nucleotide bias in the nonenzymatic copying of RNA templates, biorxiv.org

astrobiology

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