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An expanded class of histidine-accepting viral tRNA-like structures
Structured RNA elements are common in the genomes of RNA viruses, often playing critical roles during viral infection. Some viral RNA elements use forms of tRNA mimicry, but the diverse ways this mimicry can be achieved are poorly understood. Histidine-accepting tRNA-like structures (TLS(His)) are e...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8127992/ https://www.ncbi.nlm.nih.gov/pubmed/33811147 http://dx.doi.org/10.1261/rna.078550.120 |
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author | Langeberg, Conner J. Sherlock, Madeline E. MacFadden, Andrea Kieft, Jeffrey S. |
author_facet | Langeberg, Conner J. Sherlock, Madeline E. MacFadden, Andrea Kieft, Jeffrey S. |
author_sort | Langeberg, Conner J. |
collection | PubMed |
description | Structured RNA elements are common in the genomes of RNA viruses, often playing critical roles during viral infection. Some viral RNA elements use forms of tRNA mimicry, but the diverse ways this mimicry can be achieved are poorly understood. Histidine-accepting tRNA-like structures (TLS(His)) are examples found at the 3′ termini of some positive-sense single-stranded RNA (+ssRNA) viruses where they interact with several host proteins, induce histidylation of the RNA genome, and facilitate processes important for infection, to include genome replication. As only five TLS(His) examples had been reported, we explored the possible larger phylogenetic distribution and diversity of this TLS class using bioinformatic approaches. We identified many new examples of TLS(His), yielding a rigorous consensus sequence and secondary structure model that we validated by chemical probing of representative TLS(His) RNAs. We confirmed new examples as authentic TLS(His) by demonstrating their ability to be histidylated in vitro, then used mutational analyses to imply a tertiary interaction that is likely analogous to the D- and T-loop interaction found in canonical tRNAs. These results expand our understanding of how diverse RNA sequences achieve tRNA-like structure and function in the context of viral RNA genomes and lay the groundwork for high-resolution structural studies of tRNA mimicry by histidine-accepting TLSs. |
format | Online Article Text |
id | pubmed-8127992 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cold Spring Harbor Laboratory Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-81279922022-06-01 An expanded class of histidine-accepting viral tRNA-like structures Langeberg, Conner J. Sherlock, Madeline E. MacFadden, Andrea Kieft, Jeffrey S. RNA Report Structured RNA elements are common in the genomes of RNA viruses, often playing critical roles during viral infection. Some viral RNA elements use forms of tRNA mimicry, but the diverse ways this mimicry can be achieved are poorly understood. Histidine-accepting tRNA-like structures (TLS(His)) are examples found at the 3′ termini of some positive-sense single-stranded RNA (+ssRNA) viruses where they interact with several host proteins, induce histidylation of the RNA genome, and facilitate processes important for infection, to include genome replication. As only five TLS(His) examples had been reported, we explored the possible larger phylogenetic distribution and diversity of this TLS class using bioinformatic approaches. We identified many new examples of TLS(His), yielding a rigorous consensus sequence and secondary structure model that we validated by chemical probing of representative TLS(His) RNAs. We confirmed new examples as authentic TLS(His) by demonstrating their ability to be histidylated in vitro, then used mutational analyses to imply a tertiary interaction that is likely analogous to the D- and T-loop interaction found in canonical tRNAs. These results expand our understanding of how diverse RNA sequences achieve tRNA-like structure and function in the context of viral RNA genomes and lay the groundwork for high-resolution structural studies of tRNA mimicry by histidine-accepting TLSs. Cold Spring Harbor Laboratory Press 2021-06 /pmc/articles/PMC8127992/ /pubmed/33811147 http://dx.doi.org/10.1261/rna.078550.120 Text en © 2021 Langeberg et al.; Published by Cold Spring Harbor Laboratory Press for the RNA Society https://creativecommons.org/licenses/by-nc/4.0/This article is distributed exclusively by the RNA Society for the first 12 months after the full-issue publication date (see http://rnajournal.cshlp.org/site/misc/terms.xhtml). After 12 months, it is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) . |
spellingShingle | Report Langeberg, Conner J. Sherlock, Madeline E. MacFadden, Andrea Kieft, Jeffrey S. An expanded class of histidine-accepting viral tRNA-like structures |
title | An expanded class of histidine-accepting viral tRNA-like structures |
title_full | An expanded class of histidine-accepting viral tRNA-like structures |
title_fullStr | An expanded class of histidine-accepting viral tRNA-like structures |
title_full_unstemmed | An expanded class of histidine-accepting viral tRNA-like structures |
title_short | An expanded class of histidine-accepting viral tRNA-like structures |
title_sort | expanded class of histidine-accepting viral trna-like structures |
topic | Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8127992/ https://www.ncbi.nlm.nih.gov/pubmed/33811147 http://dx.doi.org/10.1261/rna.078550.120 |
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