Your browser doesn't support javascript.
The Short- and Long-Range RNA-RNA Interactome of SARS-CoV-2.
Ziv, Omer; Price, Jonathan; Shalamova, Lyudmila; Kamenova, Tsveta; Goodfellow, Ian; Weber, Friedemann; Miska, Eric A.
  • Ziv O; Wellcome Trust/Cancer Research UK Gurdon Institute and Department of Genetics, University of Cambridge, Cambridge CB2 1QN, UK. Electronic address: omer.ziv@gurdon.cam.ac.uk.
  • Price J; Wellcome Trust/Cancer Research UK Gurdon Institute and Department of Genetics, University of Cambridge, Cambridge CB2 1QN, UK.
  • Shalamova L; Institute for Virology, FB10-Veterinary Medicine, Justus-Liebig University, 35392 Gießen, Germany.
  • Kamenova T; Wellcome Trust/Cancer Research UK Gurdon Institute and Department of Genetics, University of Cambridge, Cambridge CB2 1QN, UK.
  • Goodfellow I; Division of Virology, Department of Pathology, University of Cambridge, Addenbrooke's Hospital, Cambridge CB2 2QQ, UK.
  • Weber F; Institute for Virology, FB10-Veterinary Medicine, Justus-Liebig University, 35392 Gießen, Germany. Electronic address: friedemann.weber@vetmed.uni-giessen.de.
  • Miska EA; Wellcome Trust/Cancer Research UK Gurdon Institute and Department of Genetics, University of Cambridge, Cambridge CB2 1QN, UK; Wellcome Sanger Institute, Wellcome Trust Genome Campus, Cambridge CB10 1SA, UK. Electronic address: eric.miska@gurdon.cam.ac.uk.
Mol Cell ; 80(6): 1067-1077.e5, 2020 12 17.
Article in English | MEDLINE | ID: covidwho-909354
Preprint
This scientific journal article is probably based on a previously available preprint. It has been identified through a machine matching algorithm, human confirmation is still pending.
See preprint
ABSTRACT
The Coronaviridae is a family of positive-strand RNA viruses that includes SARS-CoV-2, the etiologic agent of the COVID-19 pandemic. Bearing the largest single-stranded RNA genomes in nature, coronaviruses are critically dependent on long-distance RNA-RNA interactions to regulate the viral transcription and replication pathways. Here we experimentally mapped the in vivo RNA-RNA interactome of the full-length SARS-CoV-2 genome and subgenomic mRNAs. We uncovered a network of RNA-RNA interactions spanning tens of thousands of nucleotides. These interactions reveal that the viral genome and subgenomes adopt alternative topologies inside cells and engage in different interactions with host RNAs. Notably, we discovered a long-range RNA-RNA interaction, the FSE-arch, that encircles the programmed ribosomal frameshifting element. The FSE-arch is conserved in the related MERS-CoV and is under purifying selection. Our findings illuminate RNA structure-based mechanisms governing replication, discontinuous transcription, and translation of coronaviruses and will aid future efforts to develop antiviral strategies.
Subject(s)
Keywords

Full text: Available Collection: International databases Database: MEDLINE Main subject: Virus Replication / RNA, Viral / Genome, Viral / Frameshifting, Ribosomal / SARS-CoV-2 / COVID-19 Type of study: Etiology study Limits: Animals / Humans Language: English Journal: Mol Cell Journal subject: Molecular Biology Year: 2020 Document Type: Article

Similar

MEDLINE

...
LILACS

LIS


Full text: Available Collection: International databases Database: MEDLINE Main subject: Virus Replication / RNA, Viral / Genome, Viral / Frameshifting, Ribosomal / SARS-CoV-2 / COVID-19 Type of study: Etiology study Limits: Animals / Humans Language: English Journal: Mol Cell Journal subject: Molecular Biology Year: 2020 Document Type: Article