Evidence map›Paper›PMID 29144403›Full record

ArticleViruses2017

The Non-Homologous End Joining Protein PAXX Acts to Restrict HSV-1 Infection.

Ben J Trigg, Katharina B Lauer, Paula Fernandes Dos Santos, Heather Coleman, Gabriel Balmus, Daniel S Mansur, Brian J Ferguson

Open access · goldAbstract read
In one paragraph

Article in Viruses, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

8 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Review
  6. Early Nuclear Events after Herpesviral Infection.Journal of clinical medicine · 2019
    Review
  7. Coalescing replication compartments provide the opportunity for recombination between coinfecting herpesviruses.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2019
    Article
  8. Review
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

7 authors at 2 institutions in 2 countries.

Ben J TriggDepartment of Pathology, University of Cambridge, Tennis Court Road, Cambridge CB2 1QP, UK. bjt40@cam.ac.uk.
Katharina B LauerDepartment of Pathology, University of Cambridge, Tennis Court Road, Cambridge CB2 1QP, UK. kbl23@cam.ac.uk.
Paula Fernandes Dos SantosLaboratory of Immunobiology, Department of Microbiology, Immunology and Parasitology, Universidade Federal de Santa Catarina, Santa Catarina 88040-900, Brazil. fernandes.santos.paula@gmail.com.
Heather ColemanDepartment of Pathology, University of Cambridge, Tennis Court Road, Cambridge CB2 1QP, UK. hmc@mole.bio.cam.ac.uk.
Gabriel BalmusWellcome Trust/Cancer Research UK Gurdon Institute, University of Cambridge, Cambridge CB2 1QN, UK. gb318@cam.ac.uk.ORCID 0000-0003-2872-4468
Daniel S MansurLaboratory of Immunobiology, Department of Microbiology, Immunology and Parasitology, Universidade Federal de Santa Catarina, Santa Catarina 88040-900, Brazil. daniel.mansur@ufsc.br.ORCID 0000-0001-6773-9334
Brian J FergusonDepartment of Pathology, University of Cambridge, Tennis Court Road, Cambridge CB2 1QP, UK. bf234@cam.ac.uk.ORCID 0000-0002-6873-1032
University of Cambridge · GBUniversidade Federal de Santa Catarina · BR

Funding

Cancer Research UK 18796Wellcome TrustWellcome Trust 201946/Z/16/Z
6 · The paper itself

Abstract

Herpes simplex virus 1 (HSV-1) has extensive interactions with the host DNA damage response (DDR) machinery that can be either detrimental or beneficial to the virus. Proteins in the homologous recombination pathway are known to be required for efficient replication of the viral genome, while different members of the classical non-homologous end-joining (c-NHEJ) pathway have opposing effects on HSV-1 infection. Here, we have investigated the role of the recently-discovered c-NHEJ component, PAXX (Paralogue of XRCC4 and XLF), which we found to be excluded from the nucleus during HSV-1 infection. We have established that cells lacking PAXX have an intact innate immune response to HSV-1 but show a defect in viral genome replication efficiency. Counterintuitively,

Indexed as

DNA End-Joining RepairAnimalsCell LineDNA-Binding ProteinsGenes, ViralGenome, ViralHerpes SimplexHerpesvirus 1, HumanHumansInterferonsMiceViral ProteinsVirionVirus ReplicationDNA-Binding ProteinsInterferonsPAXX protein, humanViral Proteinsclassical non-homologous end joiningc-NHEJDDRDNA damage responseherpes simplex virus 1HSV-1PAXX

Identifiers

PMID29144403
PMCPMC5707549
OpenAlexW2769393643

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.