Evidence map›Paper›PMID 25525796›Full record

ArticleCell host & microbe2014

Adenovirus small E1A employs the lysine acetylases p300/CBP and tumor suppressor Rb to repress select host genes and promote productive virus infection.

Roberto Ferrari, Dawei Gou, Gauri Jawdekar, Sarah A Johnson, Miguel Nava, Trent Su, Ahmed F Yousef, Nathan R Zemke, Matteo Pellegrini, Siavash K Kurdistani and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell host & microbe, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed
8.4field-weighted citation impact, top 2% 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

85 citing papers in PubMed, 107 citations in OpenAlex.

  1. Article
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  4. Detection of AdenoviralInternational journal of molecular sciences · 2026
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  12. Review
  13. Identification of a novel, pathogenicFrontiers in genetics · 2025
    Article
  14. Review
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  18. Review
  19. Article
  20. Article

25 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

11 authors at 2 institutions in 1 country.

Roberto FerrariEli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research, UCLA David Geffen School of Medicine, Los Angeles, CA 90095-1570, USA.
Dawei GouMolecular Biology Institute, UCLA David Geffen School of Medicine, Los Angeles, CA 90095-1570, USA; Department of Microbiology, Immunology and Molecular Genetics, UCLA David Geffen School of Medicine, Los Angeles, CA 90095-1570, USA.
Gauri JawdekarMolecular Biology Institute, UCLA David Geffen School of Medicine, Los Angeles, CA 90095-1570, USA.
Sarah A JohnsonMolecular Biology Institute, UCLA David Geffen School of Medicine, Los Angeles, CA 90095-1570, USA.
Miguel NavaDepartment of Microbiology, Immunology and Molecular Genetics, UCLA David Geffen School of Medicine, Los Angeles, CA 90095-1570, USA.
Trent SuDepartment of Biological Chemistry, UCLA David Geffen School of Medicine, Los Angeles, CA 90095-1570, USA.
Ahmed F YousefMolecular Biology Institute, UCLA David Geffen School of Medicine, Los Angeles, CA 90095-1570, USA.
Nathan R ZemkeMolecular Biology Institute, UCLA David Geffen School of Medicine, Los Angeles, CA 90095-1570, USA.
Matteo PellegriniEli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research, UCLA David Geffen School of Medicine, Los Angeles, CA 90095-1570, USA; Molecular Biology Institute, UCLA David Geffen School of Medicine, Los Angeles, CA 90095-1570, USA; Department of Molecular, Cellular, and Developmental Biology, UCLA David Geffen School of Medicine, Los Angeles, CA 90095-1570, USA.
Siavash K KurdistaniEli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research, UCLA David Geffen School of Medicine, Los Angeles, CA 90095-1570, USA; Molecular Biology Institute, UCLA David Geffen School of Medicine, Los Angeles, CA 90095-1570, USA; Department of Biological Chemistry, UCLA David Geffen School of Medicine, Los Angeles, CA 90095-1570, USA; Department of Pathology and Laboratory of Medicine, UCLA David Geffen School of Medicine, Los Angeles, CA 90095-1570, USA.
Arnold J BerkMolecular Biology Institute, UCLA David Geffen School of Medicine, Los Angeles, CA 90095-1570, USA; Department of Microbiology, Immunology and Molecular Genetics, UCLA David Geffen School of Medicine, Los Angeles, CA 90095-1570, USA. Electronic address: berk@mbi.ucla.edu.
University of California, Los Angeles · USBroad Center · US

Funding

UCLA NIGMS T32 Program AssessmentT32GM007185 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI TORRES, JORGE · 1985 to 2020
$21.7M
Training Grant in Genomic Analysis and InterpretationT32HG002536 · NHGRI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Valerie A Arboleda, Harold Pimentel · 2002 to 2026
$8.6M
BIOSYNTHESIS OF ADENOVIRUS EARLY RNASR37CA025235 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BERK, ARNOLD J · 1987 to 2011
$7.8M
Interdisciplinary Training in Virology and Gene TherapyT32AI060567 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI WU, TING-TING · 2004 to 2018
$3.4M
BIOSYNTHESIS OF ADENOVIRUS EARLY RNASR01CA025235 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI BERK, ARNOLD J · 1985 to 2016
$2.7M
Discovery of gut microbiota-targeted small molecules: new tools and therapeuticsDP2OD006515 · OD · STANFORD UNIVERSITY · PI SONNENBURG, JUSTIN L · 2009 to 2009
$2.4M
DNA methylation and its relationship to gene expression and physiologic traitsR01GM095656 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI PELLEGRINI, MATTEO · 2011 to 2014
$1.8M
NCI NIH HHS CA25235NCI NIH HHS R01 CA025235NCI NIH HHS R37 CA025235NHGRI NIH HHS T32 HG002536NHGRI NIH HHS T32HG02536NIAID NIH HHS T32 AI060567NIAID NIH HHS T32AI060567NIGMS NIH HHS GM095656NIGMS NIH HHS R01 GM095656NIGMS NIH HHS T32 GM007185NIGMS NIH HHS T32GM007185NIH HHS 1-DP2-OD006515NIH HHS DP2 OD006515
6 · The paper itself

Abstract

Oncogenic transformation by adenovirus small e1a depends on simultaneous interactions with the host lysine acetylases p300/CBP and the tumor suppressor RB. How these interactions influence cellular gene expression remains unclear. We find that e1a displaces RBs from E2F transcription factors and promotes p300 acetylation of RB1 K873/K874 to lock it into a repressing conformation that interacts with repressive chromatin-modifying enzymes. These repressing p300-e1a-RB1 complexes specifically interact with host genes that have unusually high p300 association within the gene body. The TGF-β, TNF-, and interleukin-signaling pathway components are enriched among such p300-targeted genes. The p300-e1a-RB1 complex condenses chromatin in a manner dependent on HDAC activity, p300 lysine acetylase activity, the p300 bromodomain, and RB K873/K874 and e1a K239 acetylation to repress host genes that would otherwise inhibit productive virus infection. Thus, adenovirus employs e1a to repress host genes that interfere with viral replication.

Indexed as

AdenoviridaeAdenovirus E1A ProteinsCells, CulturedCell Transformation, ViralChemokine CXCL1ChromatinGene Expression RegulationHost-Pathogen InteractionsHumansp300-CBP Transcription FactorsPromoter Regions, GeneticRetinoblastoma ProteinRNA, MessengerSequence Analysis, RNASignal TransductionVirus ReplicationAdenovirus E1A ProteinsChemokine CXCL1ChromatinCXCL1 protein, humanp300-CBP Transcription FactorsRetinoblastoma ProteinRNA, Messenger

Identifiers

PMID25525796
PMCPMC4418520
OpenAlexW2170550202

What OpenQuestion holds

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Registered trials

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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.