Evidence map›Paper›PMID 35244721›Full record

ArticleNucleic acids research2022

Nanopore ReCappable sequencing maps SARS-CoV-2 5' capping sites and provides new insights into the structure of sgRNAs.

Camilla Ugolini, Logan Mulroney, Adrien Leger, Matteo Castelli, Elena Criscuolo, Maia Kavanagh Williamson, Andrew D Davidson, Abdulaziz Almuqrin, Roberto Giambruno, Miten Jain and 15 more

Abstract read
In one paragraph

Article in Nucleic acids research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Highly Recurrent Multinucleotide Mutations in SARS-CoV-2.Molecular biology and evolution · 2025
    Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Nanopore Guided Annotation of Transcriptome Architectures.bioRxiv : the preprint server for biology · 2024
    Article
  14. Article
  15. Article
  16. The Local Anaesthetic Procaine Prodrugs ProcClusterInternational journal of molecular sciences · 2023
    Article
  17. Review
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

25 authors.

Camilla UgoliniCenter for Genomic Science of IIT@SEMM, Fondazione Istituto Italiano di Tecnologia, 20139 Milano, Italy.ORCID 0000-0003-2269-2071
Logan MulroneyCenter for Genomic Science of IIT@SEMM, Fondazione Istituto Italiano di Tecnologia, 20139 Milano, Italy.ORCID 0000-0002-0534-0165
Adrien LegerEuropean Molecular Biology Laboratory, European Bioinformatics Institute, Hinxton, UK.ORCID 0000-0001-8772-6776
Matteo CastelliLaboratory of Microbiology and Virology, Vita-Salute San Raffaele University; via Olgettina 58, 20132 Milan, Italy.ORCID 0000-0003-0295-7941
Elena CriscuoloLaboratory of Microbiology and Virology, Vita-Salute San Raffaele University; via Olgettina 58, 20132 Milan, Italy.ORCID 0000-0003-0185-3147
Maia Kavanagh WilliamsonSchool of Cellular and Molecular Medicine, Faculty of Life Sciences, University Walk, University of Bristol, Bristol BS8 1TD, UK.ORCID 0000-0002-4659-8613
Andrew D DavidsonSchool of Cellular and Molecular Medicine, Faculty of Life Sciences, University Walk, University of Bristol, Bristol BS8 1TD, UK.ORCID 0000-0002-1136-4008
Abdulaziz AlmuqrinSchool of Cellular and Molecular Medicine, Faculty of Life Sciences, University Walk, University of Bristol, Bristol BS8 1TD, UK.
Roberto GiambrunoCenter for Genomic Science of IIT@SEMM, Fondazione Istituto Italiano di Tecnologia, 20139 Milano, Italy.ORCID 0000-0002-4566-261X
Miten JainBiomolecular Engineering Department, UC Santa Cruz, CA 95064, USA.ORCID 0000-0002-4571-3982
Gianmaria FrigèDepartment of Experimental Oncology, IEO European Institute of Oncology IRCCS, 20139 Milano, Italy.ORCID 0000-0003-3253-7091
Hugh OlsenBiomolecular Engineering Department, UC Santa Cruz, CA 95064, USA.ORCID 0000-0002-7293-8853
George TzertzinisNew England Biolabs, Ipswich, MA 01938 3, USA.ORCID 0000-0001-8821-8060
Ira SchildkrautNew England Biolabs, Ipswich, MA 01938 3, USA.ORCID 0000-0002-1143-6630
Madalee G WulfNew England Biolabs, Ipswich, MA 01938 3, USA.ORCID 0000-0002-7601-413X
Ivan R CorrêaNew England Biolabs, Ipswich, MA 01938 3, USA.ORCID 0000-0002-3169-6878
Laurence EttwillerNew England Biolabs, Ipswich, MA 01938 3, USA.ORCID 0000-0002-3957-6539
Nicola ClementiLaboratory of Microbiology and Virology, Vita-Salute San Raffaele University; via Olgettina 58, 20132 Milan, Italy.
Massimo ClementiLaboratory of Microbiology and Virology, Vita-Salute San Raffaele University; via Olgettina 58, 20132 Milan, Italy.ORCID 0000-0002-7461-5898
Nicasio ManciniLaboratory of Microbiology and Virology, Vita-Salute San Raffaele University; via Olgettina 58, 20132 Milan, Italy.ORCID 0000-0003-0637-0910
Ewan BirneyEuropean Molecular Biology Laboratory, European Bioinformatics Institute, Hinxton, UK.ORCID 0000-0001-8314-8497
Mark AkesonBiomolecular Engineering Department, UC Santa Cruz, CA 95064, USA.ORCID 0000-0001-9392-8075
Francesco NicassioCenter for Genomic Science of IIT@SEMM, Fondazione Istituto Italiano di Tecnologia, 20139 Milano, Italy.ORCID 0000-0002-5954-5318
David A MatthewsSchool of Cellular and Molecular Medicine, Faculty of Life Sciences, University Walk, University of Bristol, Bristol BS8 1TD, UK.ORCID 0000-0003-4611-8795
Tommaso LeonardiCenter for Genomic Science of IIT@SEMM, Fondazione Istituto Italiano di Tecnologia, 20139 Milano, Italy.ORCID 0000-0002-4449-1863

Funding

A Unified Nanopore Platform for Direct Sequencing of Individual Full Length RNA Strands Bearing Modified NucleotidesR01HG010053 · NHGRI · UNIVERSITY OF CALIFORNIA SANTA CRUZ · PI AKESON, MARK A · 2018 to 2021
$3.8M
Medical Research Council MR/R020566/1NHGRI NIH HHS R01 HG010053
6 · The paper itself

Abstract

The SARS-CoV-2 virus has a complex transcriptome characterised by multiple, nested subgenomic RNAsused to express structural and accessory proteins. Long-read sequencing technologies such as nanopore direct RNA sequencing can recover full-length transcripts, greatly simplifying the assembly of structurally complex RNAs. However, these techniques do not detect the 5' cap, thus preventing reliable identification and quantification of full-length, coding transcript models. Here we used Nanopore ReCappable Sequencing (NRCeq), a new technique that can identify capped full-length RNAs, to assemble a complete annotation of SARS-CoV-2 sgRNAs and annotate the location of capping sites across the viral genome. We obtained robust estimates of sgRNA expression across cell lines and viral isolates and identified novel canonical and non-canonical sgRNAs, including one that uses a previously un-annotated leader-to-body junction site. The data generated in this work constitute a useful resource for the scientific community and provide important insights into the mechanisms that regulate the transcription of SARS-CoV-2 sgRNAs.

Indexed as

COVID-19NanoporesGenome, ViralHumansRNA CapsRNA, ViralSARS-CoV-2RNA CapsRNA, Viral

Identifiers

PMID35244721
PMCPMC8989550

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.