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Third-generation Sequencing Reveals Extensive Polycistronism and Transcriptional Overlapping in a Baculovirus
The Autographa californica multiple nucleopolyhedrovirus (AcMNPV) is an insect-pathogen baculovirus. In this study, we applied the Oxford Nanopore Technologies platform for the analysis of the polyadenylated fraction of the viral transcriptome using both cDNA and direct RNA sequencing methods. We id...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5988703/ https://www.ncbi.nlm.nih.gov/pubmed/29872099 http://dx.doi.org/10.1038/s41598-018-26955-8 |
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author | Moldován, Norbert Tombácz, Dóra Szűcs, Attila Csabai, Zsolt Balázs, Zsolt Kis, Emese Molnár, Judit Boldogkői, Zsolt |
author_facet | Moldován, Norbert Tombácz, Dóra Szűcs, Attila Csabai, Zsolt Balázs, Zsolt Kis, Emese Molnár, Judit Boldogkői, Zsolt |
author_sort | Moldován, Norbert |
collection | PubMed |
description | The Autographa californica multiple nucleopolyhedrovirus (AcMNPV) is an insect-pathogen baculovirus. In this study, we applied the Oxford Nanopore Technologies platform for the analysis of the polyadenylated fraction of the viral transcriptome using both cDNA and direct RNA sequencing methods. We identified and annotated altogether 132 novel transcripts and transcript isoforms, including 4 coding and 4 non-coding RNA molecules, 47 length variants, 5 splice isoforms, as well as 23 polycistronic and 49 complex transcripts. All of the identified novel protein-coding genes were 5′-truncated forms of longer host genes. In this work, we demonstrated that in the case of transcript start site isoforms, the promoters and the initiator sequence of the longer and shorter variants belong to the same kinetic class. Long-read sequencing also revealed a complex meshwork of transcriptional overlaps, the function of which needs to be clarified. Additionally, we developed bioinformatics methods to improve the transcript annotation and to eliminate the non-specific transcription reads generated by template switching and false priming. |
format | Online Article Text |
id | pubmed-5988703 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59887032018-06-20 Third-generation Sequencing Reveals Extensive Polycistronism and Transcriptional Overlapping in a Baculovirus Moldován, Norbert Tombácz, Dóra Szűcs, Attila Csabai, Zsolt Balázs, Zsolt Kis, Emese Molnár, Judit Boldogkői, Zsolt Sci Rep Article The Autographa californica multiple nucleopolyhedrovirus (AcMNPV) is an insect-pathogen baculovirus. In this study, we applied the Oxford Nanopore Technologies platform for the analysis of the polyadenylated fraction of the viral transcriptome using both cDNA and direct RNA sequencing methods. We identified and annotated altogether 132 novel transcripts and transcript isoforms, including 4 coding and 4 non-coding RNA molecules, 47 length variants, 5 splice isoforms, as well as 23 polycistronic and 49 complex transcripts. All of the identified novel protein-coding genes were 5′-truncated forms of longer host genes. In this work, we demonstrated that in the case of transcript start site isoforms, the promoters and the initiator sequence of the longer and shorter variants belong to the same kinetic class. Long-read sequencing also revealed a complex meshwork of transcriptional overlaps, the function of which needs to be clarified. Additionally, we developed bioinformatics methods to improve the transcript annotation and to eliminate the non-specific transcription reads generated by template switching and false priming. Nature Publishing Group UK 2018-06-05 /pmc/articles/PMC5988703/ /pubmed/29872099 http://dx.doi.org/10.1038/s41598-018-26955-8 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Moldován, Norbert Tombácz, Dóra Szűcs, Attila Csabai, Zsolt Balázs, Zsolt Kis, Emese Molnár, Judit Boldogkői, Zsolt Third-generation Sequencing Reveals Extensive Polycistronism and Transcriptional Overlapping in a Baculovirus |
title | Third-generation Sequencing Reveals Extensive Polycistronism and Transcriptional Overlapping in a Baculovirus |
title_full | Third-generation Sequencing Reveals Extensive Polycistronism and Transcriptional Overlapping in a Baculovirus |
title_fullStr | Third-generation Sequencing Reveals Extensive Polycistronism and Transcriptional Overlapping in a Baculovirus |
title_full_unstemmed | Third-generation Sequencing Reveals Extensive Polycistronism and Transcriptional Overlapping in a Baculovirus |
title_short | Third-generation Sequencing Reveals Extensive Polycistronism and Transcriptional Overlapping in a Baculovirus |
title_sort | third-generation sequencing reveals extensive polycistronism and transcriptional overlapping in a baculovirus |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5988703/ https://www.ncbi.nlm.nih.gov/pubmed/29872099 http://dx.doi.org/10.1038/s41598-018-26955-8 |
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