Evidence map›Paper›PMID 31694936›Full record

ArticleJournal of virology2020

Identifying the Cellular Interactome of Epstein-Barr Virus Lytic Regulator Zta Reveals Cellular Targets Contributing to Viral Replication.

Yaqi Zhou, Kate Heesom, Kay Osborn, Rajaei AlMohammed, Steve M Sweet, Alison J Sinclair

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
0.6field-weighted citation impact, top 28% 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

12 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Epstein-barr virus (EBV) in cervical carcinoma detected by in situ hybridization targeting ebers and the viral genome.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology] · 2025
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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

6 authors at 2 institutions in 1 country.

Yaqi ZhouSchool of Life Sciences, University of Sussex, Brighton, United Kingdom.
Kate HeesomUniversity of Bristol Proteomics Facility, University of Bristol, Bristol, United Kingdom.
Kay OsbornSchool of Life Sciences, University of Sussex, Brighton, United Kingdom.
Rajaei AlMohammedSchool of Life Sciences, University of Sussex, Brighton, United Kingdom.
Steve M SweetSchool of Life Sciences, University of Sussex, Brighton, United Kingdom.
Alison J SinclairSchool of Life Sciences, University of Sussex, Brighton, United Kingdom a.j.sinclair@sussex.ac.uk.ORCID 0000-0001-8510-8691
University of Sussex · GBUniversity of Bristol · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The human gammaherpesvirus Epstein-Barr virus (EBV) (human herpesvirus 4 [HHV4]) infects most adults and is an important contributor to the development of many types of lymphoid and epithelial cancers. Essential contributions of viral genes to viral replication are known, but the potential contributions of cell genes are less well delineated. A key player is the viral protein Zta (BZLF1, ZEBRA, or Z). This sequence-specific DNA-binding protein can disrupt EBV latency by driving the transcription of target genes and by interacting with the EBV lytic origin of replication. Here, we used an unbiased proteomics approach to identify the Zta-interactome in cells derived from Burkitt's lymphoma. Isolating Zta and associated proteins from Burkitt's lymphoma cells undergoing EBV replication, followed by tandem mass tag (TMT) mass spectrometry, resulted in the identification of 39 viral and cellular proteins within the Zta interactome. An association of Zta with the cellular protein NFATc2 was validated in independent experiments. Furthermore, the ability of Zta to attenuate the activity of an NFAT-dependent promoter was shown, which suggests a functional consequence for the association. The expression of Zta is itself regulated through NFAT activity, suggesting that Zta may contribute to a feedback loop that would limit its own expression, thus aiding viral replication by preventing the known toxic effects of Zta overexpression.

Indexed as

Gene Expression Regulation, ViralBurkitt LymphomaCell LineDNA-Binding ProteinsGenes, ViralHerpesvirus 4, HumanHumansNFATC Transcription FactorsPromoter Regions, GeneticProteomicsTrans-ActivatorsViral ProteinsVirus LatencyVirus ReplicationBZLF1 protein, Herpesvirus 4, HumanDNA-Binding ProteinsNFATC2 protein, humanNFATC Transcription FactorsTrans-ActivatorsViral ProteinsEpstein-Barr virusproteomicstranscriptional regulation

Identifiers

PMID31694936
PMCPMC7000981
OpenAlexW2988563408

What OpenQuestion holds

Textmetadata
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.