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Exploiting tRNAs to Boost Virulence
Transfer RNAs (tRNAs) are powerful small RNA entities that are used to translate nucleotide language of genes into the amino acid language of proteins. Their near-uniform length and tertiary structure as well as their high nucleotide similarity and post-transcriptional modifications have made it dif...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4810235/ https://www.ncbi.nlm.nih.gov/pubmed/26797637 http://dx.doi.org/10.3390/life6010004 |
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author | Albers, Suki Czech, Andreas |
author_facet | Albers, Suki Czech, Andreas |
author_sort | Albers, Suki |
collection | PubMed |
description | Transfer RNAs (tRNAs) are powerful small RNA entities that are used to translate nucleotide language of genes into the amino acid language of proteins. Their near-uniform length and tertiary structure as well as their high nucleotide similarity and post-transcriptional modifications have made it difficult to characterize individual species quantitatively. However, due to the central role of the tRNA pool in protein biosynthesis as well as newly emerging roles played by tRNAs, their quantitative assessment yields important information, particularly relevant for virus research. Viruses which depend on the host protein expression machinery have evolved various strategies to optimize tRNA usage—either by adapting to the host codon usage or encoding their own tRNAs. Additionally, several viruses bear tRNA-like elements (TLE) in the 5′- and 3′-UTR of their mRNAs. There are different hypotheses concerning the manner in which such structures boost viral protein expression. Furthermore, retroviruses use special tRNAs for packaging and initiating reverse transcription of their genetic material. Since there is a strong specificity of different viruses towards certain tRNAs, different strategies for recruitment are employed. Interestingly, modifications on tRNAs strongly impact their functionality in viruses. Here, we review those intersection points between virus and tRNA research and describe methods for assessing the tRNA pool in terms of concentration, aminoacylation and modification. |
format | Online Article Text |
id | pubmed-4810235 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-48102352016-04-04 Exploiting tRNAs to Boost Virulence Albers, Suki Czech, Andreas Life (Basel) Review Transfer RNAs (tRNAs) are powerful small RNA entities that are used to translate nucleotide language of genes into the amino acid language of proteins. Their near-uniform length and tertiary structure as well as their high nucleotide similarity and post-transcriptional modifications have made it difficult to characterize individual species quantitatively. However, due to the central role of the tRNA pool in protein biosynthesis as well as newly emerging roles played by tRNAs, their quantitative assessment yields important information, particularly relevant for virus research. Viruses which depend on the host protein expression machinery have evolved various strategies to optimize tRNA usage—either by adapting to the host codon usage or encoding their own tRNAs. Additionally, several viruses bear tRNA-like elements (TLE) in the 5′- and 3′-UTR of their mRNAs. There are different hypotheses concerning the manner in which such structures boost viral protein expression. Furthermore, retroviruses use special tRNAs for packaging and initiating reverse transcription of their genetic material. Since there is a strong specificity of different viruses towards certain tRNAs, different strategies for recruitment are employed. Interestingly, modifications on tRNAs strongly impact their functionality in viruses. Here, we review those intersection points between virus and tRNA research and describe methods for assessing the tRNA pool in terms of concentration, aminoacylation and modification. MDPI 2016-01-19 /pmc/articles/PMC4810235/ /pubmed/26797637 http://dx.doi.org/10.3390/life6010004 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons by Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Albers, Suki Czech, Andreas Exploiting tRNAs to Boost Virulence |
title | Exploiting tRNAs to Boost Virulence |
title_full | Exploiting tRNAs to Boost Virulence |
title_fullStr | Exploiting tRNAs to Boost Virulence |
title_full_unstemmed | Exploiting tRNAs to Boost Virulence |
title_short | Exploiting tRNAs to Boost Virulence |
title_sort | exploiting trnas to boost virulence |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4810235/ https://www.ncbi.nlm.nih.gov/pubmed/26797637 http://dx.doi.org/10.3390/life6010004 |
work_keys_str_mv | AT alberssuki exploitingtrnastoboostvirulence AT czechandreas exploitingtrnastoboostvirulence |