Evidence map›Paper›PMID 9632763›Full record

ArticleMolecular and cellular biology1998

Cytomegalovirus activates interferon immediate-early response gene expression and an interferon regulatory factor 3-containing interferon-stimulated response element-binding complex.

L Navarro, K Mowen, S Rodems, B Weaver, N Reich, D Spector, M David

Open access · bronzeAbstract read
In one paragraph

Article in Molecular and cellular biology, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

70 citing papers in PubMed, 160 citations in OpenAlex.

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10 more citing papers are in PubMed but not listed here.

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 1 country.

L NavarroDepartment of Biology, University of California at San Diego, La Jolla, California 92093, USA.
K Mowen
S Rodems
B Weaver
N Reich
D Spector
M David
University of California San Diego · USState University of New York · US

Funding

HOPE Training GrantT32AI007384 · NIAID · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Sara Gianella Weibel, Scott L Letendre · 1990 to 2026
$9.7M
Human Cytomegalovirus Gene ExpressionR01CA034729 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SPECTOR, DEBORAH HYE · 1985 to 2011
$4.8M
CELLULAR &ONCOGENIC CONTROL OF INTERFERON INDUCED GENESR01CA050773 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI REICH, NANCY C. · 1995 to 2004
$1.3M
CELLULAR &ONCOGENIC CONTROL OF INTERFERON INDUCED GENESR29CA050773 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI REICH, NANCY C. · 1990 to 1994
–
NCI NIH HHS CA34729NCI NIH HHS CA50773NCI NIH HHS R01 CA034729NCI NIH HHS R01 CA050773NIAID NIH HHS AI07384NIAID NIH HHS T32 AI007384
6 · The paper itself

Abstract

Interferon establishes an antiviral state in numerous cell types through the induction of a set of immediate-early response genes. Activation of these genes is mediated by phosphorylation of latent transcription factors of the STAT family. We found that infection of primary foreskin fibroblasts with human cytomegalovirus (HCMV) causes selective transcriptional activation of the alpha/beta-interferon-responsive ISG54 gene. However, no activation or nuclear translocation of STAT proteins was detected. Activation of ISG54 occurs independent of protein synthesis but is prevented by protein tyrosine kinase inhibitors. Further analysis revealed that HCMV infection induced the DNA binding of a novel complex, tentatively called cytomegalovirus-induced interferon-stimulated response element binding factor (CIF). CIF is composed, at least in part, of the recently identified interferon regulatory factor 3 (IRF3), but it does not contain the STAT1 and STAT2 proteins that participate in the formation of interferon-stimulated gene factor 3. IRF3, which has previously been shown to possess no intrinsic transcriptional activation potential, interacts with the transcriptional coactivator CREB binding protein, but not with p300, to form CIF. Activating interferon-stimulated genes without the need for prior synthesis of interferons might provide the host cell with a potential shortcut in the activation of its antiviral defense.

Indexed as

Gene Expression Regulation, ViralRepressor Proteins2-AminopurineApoptosis Regulatory ProteinsCell LineCycloheximideCytomegalovirusDNA-Binding ProteinseIF-2 KinaseEnzyme InhibitorsGenisteinHumansInterferon-alphaInterferon-betaInterferon Regulatory Factor-1Interferon Regulatory Factor-22-AminopurineApoptosis Regulatory ProteinsCycloheximideDNA-Binding ProteinseIF-2 KinaseEnzyme InhibitorsGenisteinIFIT2 protein, humanInterferon-alphaInterferon-betaInterferon Regulatory Factor-1Interferon Regulatory Factor-2Interferon Regulatory Factor-3IRF1 protein, humanIRF2 protein, humanIRF3 protein, humanPhosphoproteinsProtein Kinase CProtein Synthesis InhibitorsProtein-Tyrosine KinasesRepressor ProteinsRNA-Binding ProteinsSTAT1 protein, humanSTAT1 Transcription FactorSTAT2 protein, humanSTAT2 Transcription FactorStaurosporineTrans-ActivatorsTranscription Factors

Identifiers

PMID9632763
PMCPMC108963
OpenAlexW1890314278

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.