Evidence map›Paper›PMID 7769680›Full record

ArticleJournal of virology1995

Identification of cellular target genes of the Epstein-Barr virus transactivator Zta: activation of transforming growth factor beta igh3 (TGF-beta igh3) and TGF-beta 1.

C Cayrol, E K Flemington

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

40 citing papers in PubMed, 100 citations in OpenAlex.

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  11. The interaction between mitochondria and oncoviruses.Biochimica et biophysica acta. Molecular basis of disease · 2018
    Review
  12. Article
  13. Review
  14. Article
  15. Article
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  17. Modulation of lung inflammation by the Epstein-Barr virus protein Zta.American journal of physiology. Lung cellular and molecular physiology · 2010
    Article
  18. Article
  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

2 authors at 2 institutions in 1 country.

C CayrolDivision of Tumor Virology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, Massachusetts 02115, USA.
E K Flemington
Dana-Farber Cancer Institute · USHarvard University · US

Funding

CHEMISTRY AND BIOLOGY OF LYMPHOCYTESR35CA047554 · NCI · HARVARD UNIVERSITY · PI STROMINGER, JACK L · 1988 to 2001
$4.7M
EPSTEIN-BARR VIRUS BZLF1 GENE PRODUCTR29GM048045 · NIGMS · DANA-FARBER CANCER INSTITUTE · PI FLEMINGTON, ERIK K · 1993 to 1997
–
NCI NIH HHS CA 47554NIGMS NIH HHS R29 GM48045
6 · The paper itself

Abstract

The lytic switch transactivator Zta initiates the ordered cascade of Epstein-Barr virus gene expression that culminates in virus production. Zta is a sequence-specific DNA-binding protein that transactivates early viral promotes via cis-acting sequences. Activation of some of these genes is mediated through binding to consensus AP-1 promoter elements. This observation suggests that Zta may also regulate the expression of cellular genes. While many targets of Zta have been identified in the Epstein-Barr virus genome, putative host cell targets remain largely unknown. To address this issue, a tetracycline-regulated Zta expression system was generated, and differential hybridization screening was used to isolate Zta-responsive cellular genes. The major target identified by this analysis is a gene encoding a fasciclin-like secreted factor, transforming growth factor beta igh3 (TGF-beta igh3), that was originally identified as a gene that is responsive to the potent immunosuppressor TGF-beta 1. Northern (RNA) blot analysis demonstrated that induction of Zta expression results in a 10-fold increase in TGF-beta igh3 mRNA levels. Zta was also found to increase TGF-beta 1 mRNA levels as well as the amount of active TGF-beta 1 secreted into the medium. Interestingly, alpha 1-collagen IV, which has been shown to potentiate the effects of TGF-beta 1, is also a cellular target of Zta. These results suggest that Zta could play a role in modulating the host cell environment through activating the expression of secreted factors.

Indexed as

Gene Expression RegulationBase SequenceDNA-Binding ProteinsHeLa CellsHerpesvirus 4, HumanHumansMolecular Sequence DataPromoter Regions, GeneticTetracyclineTrans-ActivatorsTransforming Growth Factor betaViral ProteinsBZLF1 protein, Herpesvirus 4, HumanDNA-Binding ProteinsTetracyclineTrans-ActivatorsTransforming Growth Factor betaViral Proteins

Identifiers

PMID7769680
PMCPMC189158
OpenAlexW2116109634

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.