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The Architecture of SARS-CoV-2 Transcriptome
SARS-CoV-2 is a betacoronavirus responsible for the COVID-19 pandemic. Although the SARS-CoV-2 genome was reported recently, its transcriptomic architecture is unknown. Utilizing two complementary sequencing techniques, we present a high-resolution map of the SARS-CoV-2 transcriptome and epitranscri...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7179501/ https://www.ncbi.nlm.nih.gov/pubmed/32330414 http://dx.doi.org/10.1016/j.cell.2020.04.011 |
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author | Kim, Dongwan Lee, Joo-Yeon Yang, Jeong-Sun Kim, Jun Won Kim, V. Narry Chang, Hyeshik |
author_facet | Kim, Dongwan Lee, Joo-Yeon Yang, Jeong-Sun Kim, Jun Won Kim, V. Narry Chang, Hyeshik |
author_sort | Kim, Dongwan |
collection | PubMed |
description | SARS-CoV-2 is a betacoronavirus responsible for the COVID-19 pandemic. Although the SARS-CoV-2 genome was reported recently, its transcriptomic architecture is unknown. Utilizing two complementary sequencing techniques, we present a high-resolution map of the SARS-CoV-2 transcriptome and epitranscriptome. DNA nanoball sequencing shows that the transcriptome is highly complex owing to numerous discontinuous transcription events. In addition to the canonical genomic and 9 subgenomic RNAs, SARS-CoV-2 produces transcripts encoding unknown ORFs with fusion, deletion, and/or frameshift. Using nanopore direct RNA sequencing, we further find at least 41 RNA modification sites on viral transcripts, with the most frequent motif, AAGAA. Modified RNAs have shorter poly(A) tails than unmodified RNAs, suggesting a link between the modification and the 3′ tail. Functional investigation of the unknown transcripts and RNA modifications discovered in this study will open new directions to our understanding of the life cycle and pathogenicity of SARS-CoV-2. |
format | Online Article Text |
id | pubmed-7179501 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71795012020-04-24 The Architecture of SARS-CoV-2 Transcriptome Kim, Dongwan Lee, Joo-Yeon Yang, Jeong-Sun Kim, Jun Won Kim, V. Narry Chang, Hyeshik Cell Resource SARS-CoV-2 is a betacoronavirus responsible for the COVID-19 pandemic. Although the SARS-CoV-2 genome was reported recently, its transcriptomic architecture is unknown. Utilizing two complementary sequencing techniques, we present a high-resolution map of the SARS-CoV-2 transcriptome and epitranscriptome. DNA nanoball sequencing shows that the transcriptome is highly complex owing to numerous discontinuous transcription events. In addition to the canonical genomic and 9 subgenomic RNAs, SARS-CoV-2 produces transcripts encoding unknown ORFs with fusion, deletion, and/or frameshift. Using nanopore direct RNA sequencing, we further find at least 41 RNA modification sites on viral transcripts, with the most frequent motif, AAGAA. Modified RNAs have shorter poly(A) tails than unmodified RNAs, suggesting a link between the modification and the 3′ tail. Functional investigation of the unknown transcripts and RNA modifications discovered in this study will open new directions to our understanding of the life cycle and pathogenicity of SARS-CoV-2. Elsevier Inc. 2020-05-14 2020-04-23 /pmc/articles/PMC7179501/ /pubmed/32330414 http://dx.doi.org/10.1016/j.cell.2020.04.011 Text en © 2020 Elsevier Inc. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Resource Kim, Dongwan Lee, Joo-Yeon Yang, Jeong-Sun Kim, Jun Won Kim, V. Narry Chang, Hyeshik The Architecture of SARS-CoV-2 Transcriptome |
title | The Architecture of SARS-CoV-2 Transcriptome |
title_full | The Architecture of SARS-CoV-2 Transcriptome |
title_fullStr | The Architecture of SARS-CoV-2 Transcriptome |
title_full_unstemmed | The Architecture of SARS-CoV-2 Transcriptome |
title_short | The Architecture of SARS-CoV-2 Transcriptome |
title_sort | architecture of sars-cov-2 transcriptome |
topic | Resource |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7179501/ https://www.ncbi.nlm.nih.gov/pubmed/32330414 http://dx.doi.org/10.1016/j.cell.2020.04.011 |
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