Evidence map›Paper›PMID 10846061›Full record

ArticleJournal of virology2000

The E4-6/7 protein functionally compensates for the loss of E1A expression in adenovirus infection.

R J O'Connor, P Hearing

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

19 citing papers in PubMed, 46 citations in OpenAlex.

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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

2 authors at 2 institutions in 1 country.

R J O'ConnorDepartment of Molecular Genetics and Microbiology, School of Medicine, State University of New York, Stony Brook 11794, USA.
P Hearing
State University of New York · USStony Brook University · US

Funding

TUMOR VIRUS-HOST INTERACTIONSP01CA028146 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI HEARING, PATRICK · 1986 to 2005
$9.9M
VIRAL ONCOLOGYT32CA009176 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI HEARING, PATRICK · 1985 to 2012
$5.2M
ADENOVIRUS AS A VECTOR FOR GENE THERAPYR01AI041636 · NIAID · STATE UNIVERSITY NEW YORK STONY BROOK · PI HEARING, PATRICK · 1997 to 2011
$3.6M
NCI NIH HHS CA09176NCI NIH HHS CA28146NCI NIH HHS P01 CA028146NCI NIH HHS T32 CA009176NIAID NIH HHS AI41636NIAID NIH HHS R01 AI041636
6 · The paper itself

Abstract

The E1A gene products are required and sufficient for activation of adenovirus gene expression in cultured cells. The E4-6/7 gene product induces the binding of the cellular transcription factor E2F to the viral E2a promoter region. The induction of E2F binding to the E2a promoter in vitro is directly correlated with transcriptional activation of the E2a promoter in vivo. The E2 region encodes the viral replication proteins, yet adenoviruses lacking E4-6/7 function demonstrate no defective phenotype in infected cells. Here we show that the E4-6/7 protein can functionally compensate for E1A expression in virus infection. In the absence of the E1A gene products, expression of the E4-6/7 protein is sufficient to displace retinoblastoma protein family members from E2Fs, activate expression of early region 2 via induction of E2F DNA binding to the E2a promoter region, and significantly enhance replication of an E1A-defective adenovirus. These results have implications in the regulation of viral gene expression and for the development of recombinant adenovirus vectors.

Indexed as

Adenovirus E1A ProteinsAdenovirus E4 ProteinsAdenoviruses, HumanCell LineGene DeletionGene ExpressionHeLa CellsHumansRecombinant Fusion ProteinsTumor Cells, CulturedAdenovirus E1A ProteinsAdenovirus E4 ProteinsRecombinant Fusion Proteins

Identifiers

PMID10846061
PMCPMC112076
OpenAlexW2068153306

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.