Evidence map›Paper›PMID 25747802›Full record

ArticlePLoS pathogens2015

XRN1 stalling in the 5' UTR of Hepatitis C virus and Bovine Viral Diarrhea virus is associated with dysregulated host mRNA stability.

Stephanie L Moon, Jeffrey G Blackinton, John R Anderson, Mary K Dozier, Benjamin J T Dodd, Jack D Keene, Carol J Wilusz, Shelton S Bradrick, Jeffrey Wilusz

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
23.7field-weighted citation impact, top 1% 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

56 citing papers in PubMed, 77 citations in OpenAlex.

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  13. Role of Virus-Induced Host Cell Epigenetic Changes in Cancer.International journal of molecular sciences · 2021
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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

9 authors at 3 institutions in 1 country.

Stephanie L MoonDepartment of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, Colorado, United States of America.
Jeffrey G BlackintonDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, North Carolina, United States of America.
John R AndersonDepartment of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, Colorado, United States of America.
Mary K DozierDepartment of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, Colorado, United States of America.
Benjamin J T DoddDepartment of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, Colorado, United States of America.
Jack D KeeneDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, North Carolina, United States of America.
Carol J WiluszDepartment of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, Colorado, United States of America.
Shelton S BradrickDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, North Carolina, United States of America.
Jeffrey WiluszDepartment of Microbiology, Immunology and Pathology, Colorado State University, Fort Collins, Colorado, United States of America.
Colorado State University · USDuke University Hospital · USDuke Medical Center · US

Funding

Vascular stabilization as a broad theraprutic platform for biodefenseU54AI065357 · NIAID · COLORADO STATE UNIVERSITY-FORT COLLINS · PI DOW, STEVEN W. · 2005 to 2013
$77.5M
RNA Dynamics of Transient Macromolecular Complexes in Cancer CellsR01CA157268 · NCI · DUKE UNIVERSITY · PI KEENE, JACK D · 2011 to 2015
$1.7M
Veterinary Scholars Summer Research ProgramT35OD015130 · OD · COLORADO STATE UNIVERSITY · PI ZABEL, MARK D · 2012 to 2021
$654k
Host-pathogen interactions in hepatitis C virus replicationK01DK082613 · NIDDK · DUKE UNIVERSITY · PI BRADRICK, SHELTON STEWART · 2009 to 2013
$546k
NCI NIH HHS R01 CA157268NCI NIH HHS R01CA157268NIAID NIH HHS U54 AI-065357NIAID NIH HHS U54 AI065357NIDDK NIH HHS 5-K01-DK082613NIDDK NIH HHS K01 DK082613NIH HHS T35 OD015130
6 · The paper itself

Abstract

We demonstrate that both Hepatitis C virus (HCV) and Bovine Viral Diarrhea virus (BVDV) contain regions in their 5' UTRs that stall and repress the enzymatic activity of the cellular 5'-3' exoribonuclease XRN1, resulting in dramatic changes in the stability of cellular mRNAs. We used biochemical assays, virus infections, and transfection of the HCV and BVDV 5' untranslated regions in the absence of other viral gene products to directly demonstrate the existence and mechanism of this novel host-virus interaction. In the context of HCV infection, we observed globally increased stability of mRNAs resulting in significant increases in abundance of normally short-lived mRNAs encoding a variety of relevant oncogenes and angiogenesis factors. These findings suggest that non-coding regions from multiple genera of the Flaviviridae interfere with XRN1 and impact post-transcriptional processes, causing global dysregulation of cellular gene expression which may promote cell growth and pathogenesis.

Indexed as

5' Untranslated RegionsAnimalsBlotting, WesternCattleCell LineDiarrhea Viruses, Bovine ViralExoribonucleasesHepacivirusHost-Parasite InteractionsHumansMicrotubule-Associated ProteinsPolymerase Chain ReactionRNA, MessengerRNA StabilityTransfectionVirus Replication5' Untranslated RegionsExoribonucleasesMicrotubule-Associated ProteinsRNA, MessengerXRN1 protein, human

Identifiers

PMID25747802
PMCPMC4352041
OpenAlexW2007140080

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.