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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...

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Autores principales: Kim, Dongwan, Lee, Joo-Yeon, Yang, Jeong-Sun, Kim, Jun Won, Kim, V. Narry, Chang, Hyeshik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2020
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.
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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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