Cargando…
Pyrosequencing of small non-coding RNAs in HIV-1 infected cells: evidence for the processing of a viral-cellular double-stranded RNA hybrid
Small non-coding RNAs of 18–25 nt in length can regulate gene expression through the RNA interference (RNAi) pathway. To characterize small RNAs in HIV-1-infected cells, we performed linker-ligated cloning followed by high-throughput pyrosequencing. Here, we report the composition of small RNAs in H...
Autores principales: | , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2009
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2770672/ https://www.ncbi.nlm.nih.gov/pubmed/19729508 http://dx.doi.org/10.1093/nar/gkp707 |
_version_ | 1782173698208301056 |
---|---|
author | Yeung, Man Lung Bennasser, Yamina Watashi, Koichi Le, Shu-Yun Houzet, Laurent Jeang, Kuan-Teh |
author_facet | Yeung, Man Lung Bennasser, Yamina Watashi, Koichi Le, Shu-Yun Houzet, Laurent Jeang, Kuan-Teh |
author_sort | Yeung, Man Lung |
collection | PubMed |
description | Small non-coding RNAs of 18–25 nt in length can regulate gene expression through the RNA interference (RNAi) pathway. To characterize small RNAs in HIV-1-infected cells, we performed linker-ligated cloning followed by high-throughput pyrosequencing. Here, we report the composition of small RNAs in HIV-1 productively infected MT4 T-cells. We identified several HIV-1 small RNA clones and a highly abundant small 18-nt RNA that is antisense to the HIV-1 primer-binding site (PBS). This 18-nt RNA apparently originated from the dsRNA hybrid formed by the HIV-1 PBS and the 3′ end of the human cellular tRNAlys3. It was found to associate with the Ago2 protein, suggesting its possible function in the cellular RNAi machinery for targeting HIV-1. |
format | Text |
id | pubmed-2770672 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-27706722009-10-30 Pyrosequencing of small non-coding RNAs in HIV-1 infected cells: evidence for the processing of a viral-cellular double-stranded RNA hybrid Yeung, Man Lung Bennasser, Yamina Watashi, Koichi Le, Shu-Yun Houzet, Laurent Jeang, Kuan-Teh Nucleic Acids Res RNA Small non-coding RNAs of 18–25 nt in length can regulate gene expression through the RNA interference (RNAi) pathway. To characterize small RNAs in HIV-1-infected cells, we performed linker-ligated cloning followed by high-throughput pyrosequencing. Here, we report the composition of small RNAs in HIV-1 productively infected MT4 T-cells. We identified several HIV-1 small RNA clones and a highly abundant small 18-nt RNA that is antisense to the HIV-1 primer-binding site (PBS). This 18-nt RNA apparently originated from the dsRNA hybrid formed by the HIV-1 PBS and the 3′ end of the human cellular tRNAlys3. It was found to associate with the Ago2 protein, suggesting its possible function in the cellular RNAi machinery for targeting HIV-1. Oxford University Press 2009-10 2009-09-03 /pmc/articles/PMC2770672/ /pubmed/19729508 http://dx.doi.org/10.1093/nar/gkp707 Text en © The Author(s) 2009. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.5/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | RNA Yeung, Man Lung Bennasser, Yamina Watashi, Koichi Le, Shu-Yun Houzet, Laurent Jeang, Kuan-Teh Pyrosequencing of small non-coding RNAs in HIV-1 infected cells: evidence for the processing of a viral-cellular double-stranded RNA hybrid |
title | Pyrosequencing of small non-coding RNAs in HIV-1 infected cells: evidence for the processing of a viral-cellular double-stranded RNA hybrid |
title_full | Pyrosequencing of small non-coding RNAs in HIV-1 infected cells: evidence for the processing of a viral-cellular double-stranded RNA hybrid |
title_fullStr | Pyrosequencing of small non-coding RNAs in HIV-1 infected cells: evidence for the processing of a viral-cellular double-stranded RNA hybrid |
title_full_unstemmed | Pyrosequencing of small non-coding RNAs in HIV-1 infected cells: evidence for the processing of a viral-cellular double-stranded RNA hybrid |
title_short | Pyrosequencing of small non-coding RNAs in HIV-1 infected cells: evidence for the processing of a viral-cellular double-stranded RNA hybrid |
title_sort | pyrosequencing of small non-coding rnas in hiv-1 infected cells: evidence for the processing of a viral-cellular double-stranded rna hybrid |
topic | RNA |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2770672/ https://www.ncbi.nlm.nih.gov/pubmed/19729508 http://dx.doi.org/10.1093/nar/gkp707 |
work_keys_str_mv | AT yeungmanlung pyrosequencingofsmallnoncodingrnasinhiv1infectedcellsevidencefortheprocessingofaviralcellulardoublestrandedrnahybrid AT bennasseryamina pyrosequencingofsmallnoncodingrnasinhiv1infectedcellsevidencefortheprocessingofaviralcellulardoublestrandedrnahybrid AT watashikoichi pyrosequencingofsmallnoncodingrnasinhiv1infectedcellsevidencefortheprocessingofaviralcellulardoublestrandedrnahybrid AT leshuyun pyrosequencingofsmallnoncodingrnasinhiv1infectedcellsevidencefortheprocessingofaviralcellulardoublestrandedrnahybrid AT houzetlaurent pyrosequencingofsmallnoncodingrnasinhiv1infectedcellsevidencefortheprocessingofaviralcellulardoublestrandedrnahybrid AT jeangkuanteh pyrosequencingofsmallnoncodingrnasinhiv1infectedcellsevidencefortheprocessingofaviralcellulardoublestrandedrnahybrid |