Evidence map›Paper›PMID 34634033›Full record

ArticlePLoS biology2021

SARS-CoV-2 nucleocapsid protein forms condensates with viral genomic RNA.

Amanda Jack, Luke S Ferro, Michael J Trnka, Eddie Wehri, Amrut Nadgir, Xammy H Wrynla, Douglas Fox, Katelyn Costa, Sarah Stanley, Julia Schaletzky and 1 more

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 120 papers.

0numbers the graph read from it
0cells of the map it votes in
120citing papers in PubMed
8.5field-weighted citation impact, top 2% of its field
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

120 citing papers in PubMed, 168 citations in OpenAlex.

  1. Trial
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  4. Structural Features of a Tiny Viral Protein, ORF7b of SARS-CoV-2.International journal of molecular sciences · 2026
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60 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Amanda JackBiophysics Graduate Group, University of California, Berkeley, California, United States of America.ORCID 0000-0001-8709-1432
Luke S FerroDepartment of Molecular and Cell Biology, University of California, Berkeley, California, United States of America.
Michael J TrnkaDepartment of Pharmaceutical Chemistry, University of California, San Francisco, California, United States of America.
Eddie WehriCenter for Emerging and Neglected Diseases, University of California, Berkeley, California, United States of America.
Amrut NadgirPhysics Department, University of California, Berkeley, California, United States of America.ORCID 0000-0002-6367-8148
Xammy H WrynlaSchool of Public Health, Division of Infectious Diseases and Vaccinology, University of California, Berkeley, California, United States of America.
Douglas FoxSchool of Public Health, Division of Infectious Diseases and Vaccinology, University of California, Berkeley, California, United States of America.ORCID 0000-0001-9260-4079
Katelyn CostaPress West Illustrations, Boston, Massachusetts, United States of America.
Sarah StanleyDepartment of Molecular and Cell Biology, University of California, Berkeley, California, United States of America.ORCID 0000-0002-4182-9048
Julia SchaletzkyCenter for Emerging and Neglected Diseases, University of California, Berkeley, California, United States of America.ORCID 0000-0002-7437-4684
Ahmet YildizBiophysics Graduate Group, University of California, Berkeley, California, United States of America.ORCID 0000-0003-4792-174X
University of California, Berkeley · USUniversity of California, San Francisco · US

Funding

MOLECULAR BIOPHYSICS TRAINING GRANTT32GM008295 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI HURLEY, JAMES H, WEMMER, DAVID E · 1989 to 2022
$8.1M
The Mechanism and Regulation of the Dynein Transport MachineryR35GM136414 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI Ahmet Yildiz · 2020 to 2026
$5.1M
Regulation of Microtubule Motor Proteins by TauF31GM123655 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI FERRO, LUKE S · 2017 to 2019
$119k
NIGMS NIH HHS F31 GM123655NIGMS NIH HHS R35 GM136414NIGMS NIH HHS T32 GM008295
6 · The paper itself

Abstract

The Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) infection causes Coronavirus Disease 2019 (COVID-19), a pandemic that seriously threatens global health. SARS-CoV-2 propagates by packaging its RNA genome into membrane enclosures in host cells. The packaging of the viral genome into the nascent virion is mediated by the nucleocapsid (N) protein, but the underlying mechanism remains unclear. Here, we show that the N protein forms biomolecular condensates with viral genomic RNA both in vitro and in mammalian cells. While the N protein forms spherical assemblies with homopolymeric RNA substrates that do not form base pairing interactions, it forms asymmetric condensates with viral RNA strands. Cross-linking mass spectrometry (CLMS) identified a region that drives interactions between N proteins in condensates, and deletion of this region disrupts phase separation. We also identified small molecules that alter the size and shape of N protein condensates and inhibit the proliferation of SARS-CoV-2 in infected cells. These results suggest that the N protein may utilize biomolecular condensation to package the SARS-CoV-2 RNA genome into a viral particle.

Indexed as

AnimalsCell Line, TumorChlorocebus aethiopsCoronavirus Nucleocapsid ProteinsCOVID-19Genome, ViralGenomicsHEK293 CellsHumansNucleocapsid ProteinsPhosphoproteinsProtein DomainsRNA, ViralSARS-CoV-2Vero CellsViral Genome PackagingCoronavirus Nucleocapsid Proteinsnucleocapsid phosphoprotein, SARS-CoV-2Nucleocapsid ProteinsPhosphoproteinsRNA, Viral

Identifiers

PMID34634033
PMCPMC8553124
OpenAlexW3207605229

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.