Evidence map›Paper›PMID 15681448›Full record

ArticleJournal of virology2005

Adenovirus protein VII functions throughout early phase and interacts with cellular proteins SET and pp32.

Yuming Xue, Jeffrey S Johnson, David A Ornelles, Judy Lieberman, Daniel A Engel

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

37 citing papers in PubMed, 66 citations in OpenAlex.

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  8. E3 ubiquitin ligase Mindbomb 1 facilitates nuclear delivery of adenovirus genomes.Proceedings of the National Academy of Sciences of the United States of America · 2021
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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

5 authors at 3 institutions in 1 country.

Yuming XueDepartment of Microbiology, University of Virginia Health System, Charlottesville, VA 22908, USA.
Jeffrey S Johnson
David A Ornelles
Judy Lieberman
Daniel A Engel
University of Virginia Health System · USHarvard University · USWake Forest University · US

Funding

Granzyme a Pathway of CTL-Mediated Cell DeathR01AI045587 · NIAID · IMMUNE DISEASE INSTITUTE, INC. · PI LIEBERMAN, JUDY · 1999 to 2008
$4.4M
NOVEL CELL CYCLE REGULATION BY ADENOVIRUS E1B 55KR01CA077342 · NCI · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI ORNELLES, DAVID ARNOLD · 1999 to 2009
$2.4M
ADENOVIRUS E1A PROTEIN AND THE SWI/SNF COMPLEXR01CA060675 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI ENGEL, DANIEL A · 2001 to 2005
$1.1M
Granzyme A Pathway of CTL-Mediated Cell DeathR56AI045587 · NIAID · IMMUNE DISEASE INSTITUTE, INC. · PI LIEBERMAN, JUDY · 2010 to 2010
$525k
ADENOVIRUS 243R E1A PROTEIN AND CELLULAR TRANSCRIPTIONR29CA060675 · NCI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI ENGEL, DANIEL A · 1995 to 1999
–
NCI NIH HHS CA60675NCI NIH HHS CA77342NCI NIH HHS R01 CA060675NCI NIH HHS R01 CA077342NCI NIH HHS R29 CA060675NIAID NIH HHS AI45587NIAID NIH HHS R01 AI045587NIAID NIH HHS R56 AI045587
6 · The paper itself

Abstract

Adenovirus protein VII is the major component of the viral nucleoprotein core. It is a highly basic nonspecific DNA-binding protein that condenses viral DNA inside the capsid. We have investigated the fate and function of protein VII during infection. "Input" protein VII persisted in the nucleus throughout early phase and the beginning of DNA replication. Chromatin immunoprecipitation revealed that input protein VII remained associated with viral DNA during this period. Two cellular proteins, SET and pp32, also associated with viral DNA during early phase. They are components of two multiprotein complexes, the SET and INHAT complexes, implicated in chromatin-related activities. Protein VII associated with SET and pp32 in vitro and distinct domains of protein VII were responsible for binding to the two proteins. Interestingly, protein VII was found in novel nuclear dot structures as visualized by immunofluorescence. The dots likely represent individual infectious genomes in association with protein VII. They appeared within 30 min after infection and localized in the nucleus with a peak of intensity between 4 and 10 h postinfection. After this, their intensity decreased and they disappeared between 16 and 24 h postinfection. Interestingly, disappearance of the dots required ongoing RNA synthesis but not DNA synthesis. Taken together these data indicate that protein VII has an ongoing role during early phase and the beginning of DNA replication.

Indexed as

Adenovirus E1A ProteinsAdenoviruses, HumanChromosomal Proteins, Non-HistoneDNA-Binding ProteinsHeLa CellsHistone ChaperonesHumansNuclear ProteinsPhosphoproteinsTranscription FactorsAdenovirus E1A ProteinsChromosomal Proteins, Non-HistoneDNA-Binding ProteinsHistone ChaperonesNuclear ProteinsPhosphoproteinsSET protein, humanTranscription Factors

Identifiers

PMID15681448
PMCPMC546597
OpenAlexW2118075942

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.