Evidence map›Paper›PMID 17959680›Full record

ArticleJournal of virology2008

Identification of human cytomegalovirus UL84 virus- and cell-encoded binding partners by using proteomics analysis.

Yang Gao, Kelly Colletti, Gregory S Pari

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2008. 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
4.3field-weighted citation impact, top 6% 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, 57 citations in OpenAlex.

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  14. Herpes simplex viruses: mechanisms of DNA replication.Cold Spring Harbor perspectives in biology · 2012
    Review
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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

3 authors at 1 institution in 1 country.

Yang GaoUniversity of Nevada-Reno, Department of Microbiology, Howard Bldg. 210, Reno, NV 89557, USA.
Kelly Colletti
Gregory S Pari
University of Nevada, Reno · US

Funding

UNDERGRADUATE RESEARCH AND TRAININGP20RR016464 · NCRR · UNIVERSITY OF NEVADA RENO · PI REIBER, CARL · 2001 to 2011
$30.3M
CHARACTERIZATION OF HCMV UL84R01AI045096 · NIAID · UNIVERSITY OF NEVADA RENO · PI ROSSETTO, CYPRIAN CONSTANCE · 2000 to 2014
$4.6M
NCRR NIH HHS P20 RR-016464NCRR NIH HHS P20 RR016464NIAID NIH HHS AI45096NIAID NIH HHS R01 AI045096
6 · The paper itself

Abstract

Human cytomegalovirus (HCMV) UL84 is a phosphoprotein that shuttles from the nucleus to the cytoplasm and is required for oriLyt-dependent DNA replication and viral growth. UL84 was previously shown to interact with IE2 (IE86) in infected cells, and this interaction down-regulates IE2-mediated transcriptional activation in transient assays. UL84 and IE2 were also shown to cooperatively activate a promoter within HCMV oriLyt. UL84 alone can interact with an RNA stem-loop within oriLyt and is bound to this structure within the virion. In an effort to investigate the binding partners for UL84 in infected cells, we pulled down UL84 from protein lysates prepared from HCMV-infected human fibroblasts by using a UL84-specific antibody and resolved the immunoprecipitated protein complexes by two-dimensional gel electrophoresis. We subsequently identified individual proteins by matrix-assisted laser desorption ionization-tandem time of flight analysis. This analysis revealed that UL84 interacts with viral proteins UL44, pp65, and IE2. In addition, a number of cell-encoded proteins were identified, including ubiquitin-conjugating enzyme E2, casein kinase II (CKII), and the multifunctional protein p32. We also confirmed the interaction between UL84 and IE2 as well as the interaction of UL84 with importin alpha. UL44, pp65, and CKII interactions were confirmed to occur in infected and cotransfected cells by coimmunoprecipitation assays followed by Western blotting. Ubiquitination of UL84 occurred in the presence and absence of the proteasome activity inhibitor MG132 in infected cells. The identification of UL84 binding partners is a significant step toward the understanding of the function of this significant replication protein.

Indexed as

Casein Kinase IICell LineCytomegalovirusDNA-Binding ProteinsElectrophoresis, Gel, Two-DimensionalFibroblastsHumansImmediate-Early ProteinsPhosphoproteinsProtein BindingProteomeSpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationTrans-ActivatorsUbiquitin-Conjugating EnzymesViral Matrix ProteinsViral ProteinsCasein Kinase IIcytomegalovirus matrix protein 65kDaDNA-Binding ProteinsICP36 protein, CytomegalovirusIE2 protein, CytomegalovirusImmediate-Early ProteinsPhosphoproteinsProteomeTrans-ActivatorsUbiquitin-Conjugating EnzymesUL84 protein, CytomegalovirusViral Matrix ProteinsViral Proteins

Identifiers

PMID17959680
PMCPMC2224362
OpenAlexW2115311345

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.