Publications

Detailed Information

The Architecture of SARS-CoV-2 Transcriptome

DC Field Value Language
dc.contributor.authorKim, Dongwan-
dc.contributor.authorLee, Joo-Yeon-
dc.contributor.authorYang, Jeong-Sun-
dc.contributor.authorKim, Jun Won-
dc.contributor.authorKim, V. Narry-
dc.contributor.authorChang, Hyeshik-
dc.date.accessioned2021-01-31T08:15:00Z-
dc.date.available2021-01-31T08:15:00Z-
dc.date.created2020-06-08-
dc.date.created2020-06-08-
dc.date.issued2020-05-
dc.identifier.citationCell, Vol.181 No.4, pp.914-921.e10-
dc.identifier.issn0092-8674-
dc.identifier.other102675-
dc.identifier.urihttps://hdl.handle.net/10371/171943-
dc.description.abstractSARS-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 epitran-scriptome. 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 nano pore 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.-
dc.language영어-
dc.publisherCell Press-
dc.titleThe Architecture of SARS-CoV-2 Transcriptome-
dc.typeArticle-
dc.contributor.AlternativeAuthor김빛내리-
dc.identifier.doi10.1016/j.cell.2020.04.011-
dc.citation.journaltitleCell-
dc.identifier.wosid000533623900016-
dc.identifier.scopusid2-s2.0-85083509190-
dc.citation.endpage921.e10-
dc.citation.number4-
dc.citation.startpage914-
dc.citation.volume181-
dc.identifier.sci000533623900016-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorKim, V. Narry-
dc.contributor.affiliatedAuthorChang, Hyeshik-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusRNA-SYNTHESIS-
dc.subject.keywordPlusCORONAVIRUS-
dc.subject.keywordPlusN6-METHYLADENOSINE-
dc.subject.keywordPlusGENOMES-
dc.subject.keywordAuthorcoronavirus-
dc.subject.keywordAuthorCOVID-19-
dc.subject.keywordAuthordirect RNA sequencing-
dc.subject.keywordAuthordiscontinuous transcription-
dc.subject.keywordAuthorepitranscriptome-
dc.subject.keywordAuthornanopore-
dc.subject.keywordAuthorpoly(A) tail-
dc.subject.keywordAuthorRNA modification-
dc.subject.keywordAuthorSARS-CoV-2-
dc.subject.keywordAuthortranscriptome-
Appears in Collections:
Files in This Item:

Related Researcher

  • College of Natural Sciences
  • School of Biological Sciences
Research Area Molecular Biology & Genetics

Altmetrics

Item View & Download Count

  • mendeley

Items in S-Space are protected by copyright, with all rights reserved, unless otherwise indicated.

Share