Evidence map›Paper›PMID 33083157›Full record

ArticlePeerJ2020

Mutations of SARS-CoV-2 nsp14 exhibit strong association with increased genome-wide mutation load.

Doğa Eskier, Aslı Suner, Yavuz Oktay, Gökhan Karakülah

Open access · goldAbstract read
In one paragraph

Article in PeerJ, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
1.0field-weighted citation impact, top 14% 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

31 citing papers in PubMed, 76 citations in OpenAlex.

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  18. Structure and dynamics of SARS-CoV-2 proofreading exoribonuclease ExoN.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  19. SARS-CoV-2-Specific Immune Response and the Pathogenesis of COVID-19.International journal of molecular sciences · 2022
    Review
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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

4 authors at 2 institutions in 1 country.

Doğa Eskier *Izmir Biomedicine and Genome Center, Izmir, Turkey.ORCID 0000-0003-0660-5791
Aslı Suner *Department of Biostatistics and Medical Informatics, Faculty of Medicine, Ege University, Izmir, Turkey.ORCID 0000-0002-6872-9901
Yavuz OktayIzmir Biomedicine and Genome Center, Izmir, Turkey.ORCID 0000-0002-0158-2693
Gökhan KarakülahIzmir Biomedicine and Genome Center, Izmir, Turkey.ORCID 0000-0001-6706-1375
Izmir University · TREge University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

SARS-CoV-2 is a betacoronavirus responsible for COVID-19, a pandemic with global impact that first emerged in late 2019. Since then, the viral genome has shown considerable variance as the disease spread across the world, in part due to the zoonotic origins of the virus and the human host adaptation process. As a virus with an RNA genome that codes for its own genomic replication proteins, mutations in these proteins can significantly impact the variance rate of the genome, affecting both the survival and infection rate of the virus, and attempts at combating the disease. In this study, we analyzed the mutation densities of viral isolates carrying frequently observed mutations for four proteins in the RNA synthesis complex over time in comparison to wildtype isolates. Our observations suggest mutations in nsp14, an error-correcting exonuclease protein, have the strongest association with increased mutation load without selective pressure and across the genome, compared to nsp7, nsp8 and nsp12, which form the core polymerase complex. We propose nsp14 as a priority research target for understanding genomic variance rate in SARS-CoV-2 isolates and nsp14 mutations as potential predictors for high mutability strains.

Indexed as

3′-5′ exonucleaseCOVID-19Mutation ratensp14RdRpRNA-dependent RNA polymeraseSARS-CoV-2

Identifiers

PMID33083157
PMCPMC7560320
OpenAlexW3048485609

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.