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Identification and Validation of Human Papillomavirus Encoded microRNAs
We report here identification and validation of the first papillomavirus encoded microRNAs expressed in human cervical lesions and cell lines. We established small RNA libraries from ten human papillomavirus associated cervical lesions including cancer and two human papillomavirus harboring cell lin...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3728184/ https://www.ncbi.nlm.nih.gov/pubmed/23936163 http://dx.doi.org/10.1371/journal.pone.0070202 |
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author | Qian, Kui Pietilä, Tuuli Rönty, Mikko Michon, Frederic Frilander, Mikko J. Ritari, Jarmo Tarkkanen, Jussi Paulín, Lars Auvinen, Petri Auvinen, Eeva |
author_facet | Qian, Kui Pietilä, Tuuli Rönty, Mikko Michon, Frederic Frilander, Mikko J. Ritari, Jarmo Tarkkanen, Jussi Paulín, Lars Auvinen, Petri Auvinen, Eeva |
author_sort | Qian, Kui |
collection | PubMed |
description | We report here identification and validation of the first papillomavirus encoded microRNAs expressed in human cervical lesions and cell lines. We established small RNA libraries from ten human papillomavirus associated cervical lesions including cancer and two human papillomavirus harboring cell lines. These libraries were sequenced using SOLiD 4 technology. We used the sequencing data to predict putative viral microRNAs and discovered nine putative papillomavirus encoded microRNAs. Validation was performed for five candidates, four of which were successfully validated by qPCR from cervical tissue samples and cell lines: two were encoded by HPV 16, one by HPV 38 and one by HPV 68. The expression of HPV 16 microRNAs was further confirmed by in situ hybridization, and colocalization with p16INK4A was established. Prediction of cellular target genes of HPV 16 encoded microRNAs suggests that they may play a role in cell cycle, immune functions, cell adhesion and migration, development, and cancer. Two putative viral target sites for the two validated HPV 16 miRNAs were mapped to the E5 gene, one in the E1 gene, two in the L1 gene and one in the LCR region. This is the first report to show that papillomaviruses encode their own microRNA species. Importantly, microRNAs were found in libraries established from human cervical disease and carcinoma cell lines, and their expression was confirmed in additional tissue samples. To our knowledge, this is also the first paper to use in situ hybridization to show the expression of a viral microRNA in human tissue. |
format | Online Article Text |
id | pubmed-3728184 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37281842013-08-09 Identification and Validation of Human Papillomavirus Encoded microRNAs Qian, Kui Pietilä, Tuuli Rönty, Mikko Michon, Frederic Frilander, Mikko J. Ritari, Jarmo Tarkkanen, Jussi Paulín, Lars Auvinen, Petri Auvinen, Eeva PLoS One Research Article We report here identification and validation of the first papillomavirus encoded microRNAs expressed in human cervical lesions and cell lines. We established small RNA libraries from ten human papillomavirus associated cervical lesions including cancer and two human papillomavirus harboring cell lines. These libraries were sequenced using SOLiD 4 technology. We used the sequencing data to predict putative viral microRNAs and discovered nine putative papillomavirus encoded microRNAs. Validation was performed for five candidates, four of which were successfully validated by qPCR from cervical tissue samples and cell lines: two were encoded by HPV 16, one by HPV 38 and one by HPV 68. The expression of HPV 16 microRNAs was further confirmed by in situ hybridization, and colocalization with p16INK4A was established. Prediction of cellular target genes of HPV 16 encoded microRNAs suggests that they may play a role in cell cycle, immune functions, cell adhesion and migration, development, and cancer. Two putative viral target sites for the two validated HPV 16 miRNAs were mapped to the E5 gene, one in the E1 gene, two in the L1 gene and one in the LCR region. This is the first report to show that papillomaviruses encode their own microRNA species. Importantly, microRNAs were found in libraries established from human cervical disease and carcinoma cell lines, and their expression was confirmed in additional tissue samples. To our knowledge, this is also the first paper to use in situ hybridization to show the expression of a viral microRNA in human tissue. Public Library of Science 2013-07-30 /pmc/articles/PMC3728184/ /pubmed/23936163 http://dx.doi.org/10.1371/journal.pone.0070202 Text en © 2013 Qian et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Qian, Kui Pietilä, Tuuli Rönty, Mikko Michon, Frederic Frilander, Mikko J. Ritari, Jarmo Tarkkanen, Jussi Paulín, Lars Auvinen, Petri Auvinen, Eeva Identification and Validation of Human Papillomavirus Encoded microRNAs |
title | Identification and Validation of Human Papillomavirus Encoded microRNAs |
title_full | Identification and Validation of Human Papillomavirus Encoded microRNAs |
title_fullStr | Identification and Validation of Human Papillomavirus Encoded microRNAs |
title_full_unstemmed | Identification and Validation of Human Papillomavirus Encoded microRNAs |
title_short | Identification and Validation of Human Papillomavirus Encoded microRNAs |
title_sort | identification and validation of human papillomavirus encoded micrornas |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3728184/ https://www.ncbi.nlm.nih.gov/pubmed/23936163 http://dx.doi.org/10.1371/journal.pone.0070202 |
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