A ribozyme that triphosphorylates RNA 5′-hydroxyl groups

The RNA world hypothesis describes a stage in the early evolution of life in which RNA served as genome and as the only genome-encoded catalyst. To test whether RNA world organisms could have used cyclic trimetaphosphate as an energy source, we developed an in vitro selection strategy for isolating...

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Main Authors: Moretti, Janina E., Müller, Ulrich F.
Format: Online
Language:English
Published: Oxford University Press 2014
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3985629/
id pubmed-3985629
recordtype oai_dc
spelling pubmed-39856292014-04-18 A ribozyme that triphosphorylates RNA 5′-hydroxyl groups Moretti, Janina E. Müller, Ulrich F. Synthetic Biology and Chemistry The RNA world hypothesis describes a stage in the early evolution of life in which RNA served as genome and as the only genome-encoded catalyst. To test whether RNA world organisms could have used cyclic trimetaphosphate as an energy source, we developed an in vitro selection strategy for isolating ribozymes that catalyze the triphosphorylation of RNA 5′-hydroxyl groups with trimetaphosphate. Several active sequences were isolated, and one ribozyme was analyzed in more detail. The ribozyme was truncated to 96 nt, while retaining full activity. It was converted to a trans-format and reacted with rates of 0.16 min−1 under optimal conditions. The secondary structure appears to contain a four-helical junction motif. This study showed that ribozymes can use trimetaphosphate to triphosphorylate RNA 5′-hydroxyl groups and suggested that RNA world organisms could have used trimetaphosphate as their energy source. Oxford University Press 2014-04 2014-01-21 /pmc/articles/PMC3985629/ /pubmed/24452796 http://dx.doi.org/10.1093/nar/gkt1405 Text en © The Author(s) 2014. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Moretti, Janina E.
Müller, Ulrich F.
spellingShingle Moretti, Janina E.
Müller, Ulrich F.
A ribozyme that triphosphorylates RNA 5′-hydroxyl groups
author_facet Moretti, Janina E.
Müller, Ulrich F.
author_sort Moretti, Janina E.
title A ribozyme that triphosphorylates RNA 5′-hydroxyl groups
title_short A ribozyme that triphosphorylates RNA 5′-hydroxyl groups
title_full A ribozyme that triphosphorylates RNA 5′-hydroxyl groups
title_fullStr A ribozyme that triphosphorylates RNA 5′-hydroxyl groups
title_full_unstemmed A ribozyme that triphosphorylates RNA 5′-hydroxyl groups
title_sort ribozyme that triphosphorylates rna 5′-hydroxyl groups
description The RNA world hypothesis describes a stage in the early evolution of life in which RNA served as genome and as the only genome-encoded catalyst. To test whether RNA world organisms could have used cyclic trimetaphosphate as an energy source, we developed an in vitro selection strategy for isolating ribozymes that catalyze the triphosphorylation of RNA 5′-hydroxyl groups with trimetaphosphate. Several active sequences were isolated, and one ribozyme was analyzed in more detail. The ribozyme was truncated to 96 nt, while retaining full activity. It was converted to a trans-format and reacted with rates of 0.16 min−1 under optimal conditions. The secondary structure appears to contain a four-helical junction motif. This study showed that ribozymes can use trimetaphosphate to triphosphorylate RNA 5′-hydroxyl groups and suggested that RNA world organisms could have used trimetaphosphate as their energy source.
publisher Oxford University Press
publishDate 2014
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3985629/
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