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Deep sequencing of virus-infected cells reveals HIV-encoded small RNAs
Small virus-derived interfering RNAs (viRNAs) play an important role in antiviral defence in plants, insects and nematodes by triggering the RNA interference (RNAi) pathway. The role of RNAi as an antiviral defence mechanism in mammalian cells has been obscure due to the lack of viRNA detection. Alt...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3245934/ https://www.ncbi.nlm.nih.gov/pubmed/21911362 http://dx.doi.org/10.1093/nar/gkr719 |
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author | Schopman, Nick C.T. Willemsen, Marcel Liu, Ying Poi Bradley, Ted van Kampen, Antoine Baas, Frank Berkhout, Ben Haasnoot, Joost |
author_facet | Schopman, Nick C.T. Willemsen, Marcel Liu, Ying Poi Bradley, Ted van Kampen, Antoine Baas, Frank Berkhout, Ben Haasnoot, Joost |
author_sort | Schopman, Nick C.T. |
collection | PubMed |
description | Small virus-derived interfering RNAs (viRNAs) play an important role in antiviral defence in plants, insects and nematodes by triggering the RNA interference (RNAi) pathway. The role of RNAi as an antiviral defence mechanism in mammalian cells has been obscure due to the lack of viRNA detection. Although viRNAs from different mammalian viruses have recently been identified, their functions and possible impact on viral replication remain unknown. To identify viRNAs derived from HIV-1, we used the extremely sensitive SOLiD(TM) 3 Plus System to analyse viRNA accumulation in HIV-1-infected T lymphocytes. We detected numerous small RNAs that correspond to the HIV-1 RNA genome. The majority of these sequences have a positive polarity (98.1%) and could be derived from miRNAs encoded by structured segments of the HIV-1 RNA genome (vmiRNAs). A small portion of the viRNAs is of negative polarity and most of them are encoded within the 3′-UTR, which may represent viral siRNAs (vsiRNAs). The identified vsiRNAs can potently repress HIV-1 production, whereas suppression of the vsiRNAs by antagomirs stimulate virus production. These results suggest that HIV-1 triggers the production of vsiRNAs and vmiRNAs to modulate cellular and/or viral gene expression. |
format | Online Article Text |
id | pubmed-3245934 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-32459342012-01-03 Deep sequencing of virus-infected cells reveals HIV-encoded small RNAs Schopman, Nick C.T. Willemsen, Marcel Liu, Ying Poi Bradley, Ted van Kampen, Antoine Baas, Frank Berkhout, Ben Haasnoot, Joost Nucleic Acids Res RNA Small virus-derived interfering RNAs (viRNAs) play an important role in antiviral defence in plants, insects and nematodes by triggering the RNA interference (RNAi) pathway. The role of RNAi as an antiviral defence mechanism in mammalian cells has been obscure due to the lack of viRNA detection. Although viRNAs from different mammalian viruses have recently been identified, their functions and possible impact on viral replication remain unknown. To identify viRNAs derived from HIV-1, we used the extremely sensitive SOLiD(TM) 3 Plus System to analyse viRNA accumulation in HIV-1-infected T lymphocytes. We detected numerous small RNAs that correspond to the HIV-1 RNA genome. The majority of these sequences have a positive polarity (98.1%) and could be derived from miRNAs encoded by structured segments of the HIV-1 RNA genome (vmiRNAs). A small portion of the viRNAs is of negative polarity and most of them are encoded within the 3′-UTR, which may represent viral siRNAs (vsiRNAs). The identified vsiRNAs can potently repress HIV-1 production, whereas suppression of the vsiRNAs by antagomirs stimulate virus production. These results suggest that HIV-1 triggers the production of vsiRNAs and vmiRNAs to modulate cellular and/or viral gene expression. Oxford University Press 2012-01 2011-09-10 /pmc/articles/PMC3245934/ /pubmed/21911362 http://dx.doi.org/10.1093/nar/gkr719 Text en © The Author(s) 2011. 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 unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | RNA Schopman, Nick C.T. Willemsen, Marcel Liu, Ying Poi Bradley, Ted van Kampen, Antoine Baas, Frank Berkhout, Ben Haasnoot, Joost Deep sequencing of virus-infected cells reveals HIV-encoded small RNAs |
title | Deep sequencing of virus-infected cells reveals HIV-encoded small RNAs |
title_full | Deep sequencing of virus-infected cells reveals HIV-encoded small RNAs |
title_fullStr | Deep sequencing of virus-infected cells reveals HIV-encoded small RNAs |
title_full_unstemmed | Deep sequencing of virus-infected cells reveals HIV-encoded small RNAs |
title_short | Deep sequencing of virus-infected cells reveals HIV-encoded small RNAs |
title_sort | deep sequencing of virus-infected cells reveals hiv-encoded small rnas |
topic | RNA |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3245934/ https://www.ncbi.nlm.nih.gov/pubmed/21911362 http://dx.doi.org/10.1093/nar/gkr719 |
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