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Template‐Directed Copying of RNA by Non‐enzymatic Ligation

The non‐enzymatic replication of the primordial genetic material is thought to have enabled the evolution of early forms of RNA‐based life. However, the replication of oligonucleotides long enough to encode catalytic functions is problematic due to the low efficiency of template copying with mononuc...

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Detalles Bibliográficos
Autores principales: Zhou, Lijun, O'Flaherty, Derek K., Szostak, Jack W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496532/
https://www.ncbi.nlm.nih.gov/pubmed/32558121
http://dx.doi.org/10.1002/anie.202004934
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author Zhou, Lijun
O'Flaherty, Derek K.
Szostak, Jack W.
author_facet Zhou, Lijun
O'Flaherty, Derek K.
Szostak, Jack W.
author_sort Zhou, Lijun
collection PubMed
description The non‐enzymatic replication of the primordial genetic material is thought to have enabled the evolution of early forms of RNA‐based life. However, the replication of oligonucleotides long enough to encode catalytic functions is problematic due to the low efficiency of template copying with mononucleotides. We show that template‐directed ligation can assemble long RNAs from shorter oligonucleotides, which would be easier to replicate. The rate of ligation can be greatly enhanced by employing a 3′‐amino group at the 3′‐end of each oligonucleotide, in combination with an N‐alkyl imidazole organocatalyst. These modifications enable the copying of RNA templates by the multistep ligation of tetranucleotide building blocks, as well as the assembly of long oligonucleotides using short splint oligonucleotides. We also demonstrate the formation of long oligonucleotides inside model prebiotic vesicles, which suggests a potential route to the assembly of artificial cells capable of evolution.
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spelling pubmed-74965322020-09-25 Template‐Directed Copying of RNA by Non‐enzymatic Ligation Zhou, Lijun O'Flaherty, Derek K. Szostak, Jack W. Angew Chem Int Ed Engl Research Articles The non‐enzymatic replication of the primordial genetic material is thought to have enabled the evolution of early forms of RNA‐based life. However, the replication of oligonucleotides long enough to encode catalytic functions is problematic due to the low efficiency of template copying with mononucleotides. We show that template‐directed ligation can assemble long RNAs from shorter oligonucleotides, which would be easier to replicate. The rate of ligation can be greatly enhanced by employing a 3′‐amino group at the 3′‐end of each oligonucleotide, in combination with an N‐alkyl imidazole organocatalyst. These modifications enable the copying of RNA templates by the multistep ligation of tetranucleotide building blocks, as well as the assembly of long oligonucleotides using short splint oligonucleotides. We also demonstrate the formation of long oligonucleotides inside model prebiotic vesicles, which suggests a potential route to the assembly of artificial cells capable of evolution. John Wiley and Sons Inc. 2020-08-13 2020-09-01 /pmc/articles/PMC7496532/ /pubmed/32558121 http://dx.doi.org/10.1002/anie.202004934 Text en © 2020 The Authors. Published by Wiley-VCH GmbH This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Zhou, Lijun
O'Flaherty, Derek K.
Szostak, Jack W.
Template‐Directed Copying of RNA by Non‐enzymatic Ligation
title Template‐Directed Copying of RNA by Non‐enzymatic Ligation
title_full Template‐Directed Copying of RNA by Non‐enzymatic Ligation
title_fullStr Template‐Directed Copying of RNA by Non‐enzymatic Ligation
title_full_unstemmed Template‐Directed Copying of RNA by Non‐enzymatic Ligation
title_short Template‐Directed Copying of RNA by Non‐enzymatic Ligation
title_sort template‐directed copying of rna by non‐enzymatic ligation
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496532/
https://www.ncbi.nlm.nih.gov/pubmed/32558121
http://dx.doi.org/10.1002/anie.202004934
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