Evidence map›Paper›PMID 16079238›Full record

ArticleGenetics2005

Modeling early Epstein-Barr virus infection in Drosophila melanogaster: the BZLF1 protein.

Amy L Adamson, Natasha Wright, Dennis R LaJeunesse

Open access · bronzeAbstract read
In one paragraph

Article in Genetics, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
0.9field-weighted citation impact, top 26% 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

20 citing papers in PubMed, 30 citations in OpenAlex.

  1. International journal of molecular sciences · 2025
    Review
  2. Frontiers in microbiology · 2025
    Article
  3. Article
  4. Review
  5. Article
  6. International journal of molecular sciences · 2021
    Review
  7. Potential Application ofFrontiers in pharmacology · 2020
    Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Rescue of Notch signaling in cells incapable of GDP-L-fucose synthesis by gap junction transfer of GDP-L-fucose in Drosophila.Proceedings of the National Academy of Sciences of the United States of America · 2012
    Article
  13. Review
  14. Article
  15. Article
  16. The Drosophila melanogaster host model.Journal of oral microbiology · 2012
    Article
  17. Article
  18. Russian journal of genetics · 2011
    Review
  19. Article
  20. Article
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

3 authors at 1 institution in 1 country.

Amy L AdamsonDepartment of Biology, University of North Carolina, Greensboro, North Carolina, 27402, USA. aladamso@uncg.edu
Natasha Wright
Dennis R LaJeunesse
University of North Carolina at Greensboro · US

Funding

Genetic Modifiers of Epstein-Barr Virus/Host InteractnsR21DE014602 · NIDCR · UNIVERSITY OF NORTH CAROLINA GREENSBORO · PI ADAMSON, AMY L · 2002 to 2003
$194k
NIDCR NIH HHS 1-R21-DE14602-01NIDCR NIH HHS R21 DE014602
6 · The paper itself

Abstract

Epstein-Barr virus (EBV) is the causative agent of infectious mononucleosis and is associated with several forms of cancer, including lymphomas and nasopharyngeal carcinoma. The EBV immediate-early protein BZLF1 functions as a transcriptional activator of EBV early gene expression and is essential for the viral transition between latent and lytic replication. In addition to its role in the EBV life cycle, BZLF1 (Z) also has profound effects upon the host cellular environment, including disruption of cell cycle regulation, signal transduction pathways, and transcription. In an effort to understand the nature of Z interactions with the host cellular environment, we have developed a Drosophila model of early EBV infection, where we have expressed Z in the Drosophila eye. Using this system, we have identified a highly conserved interaction between the Epstein-Barr virus Z protein and shaven, a Drosophila homolog of the human Pax2/5/8 family of genes. Pax5 is a well-characterized human gene involved with B-cell development. The B-cell-specific Pax5 also promotes the transcription of EBV latent genes from the EBV Wp promoter. Our work clearly demonstrates that the Drosophila system is an appropriate and powerful tool for identifying the underlying genetic networks involved in human infectious disease.

Indexed as

AnimalsApoptosisCell ProliferationDisease Models, AnimalDNA-Binding ProteinsDrosophila melanogasterDrosophila ProteinsEpstein-Barr Virus InfectionsEyeEye ProteinsHeLa CellsHerpesvirus 4, HumanHomeodomain ProteinsHumansLarvaNerve Tissue ProteinsBZLF1 protein, Herpesvirus 4, Humanct protein, DrosophilaDNA-Binding ProteinsDrosophila ProteinsEye ProteinsHomeodomain ProteinsNerve Tissue ProteinsNuclear ProteinsPAX5 protein, humanPAX5 Transcription Factorsv protein, DrosophilaTrans-ActivatorsTranscription FactorsViral Proteinsz protein, Drosophila

Identifiers

PMID16079238
PMCPMC1456816
OpenAlexW2104230943

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.