Evidence map›Paper›PMID 22496654›Full record

ArticlePLoS pathogens2012

Virion assembly factories in the nucleus of polyomavirus-infected cells.

Kimberly D Erickson, Cedric Bouchet-Marquis, Katie Heiser, Eva Szomolanyi-Tsuda, Rabinarayan Mishra, Benjamin Lamothe, Andreas Hoenger, Robert L Garcea

Open access · goldAbstract read
In one paragraph

Article in PLoS pathogens, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

44 citing papers in PubMed, 72 citations in OpenAlex.

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  16. Temporal compartmentalization of viral infection in bacterial cells.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

8 authors at 2 institutions in 1 country.

Kimberly D EricksonDepartment of Molecular, Cellular and Developmental Biology, University of Colorado, Boulder, Colorado, United States of America.
Cedric Bouchet-Marquis
Katie Heiser
Eva Szomolanyi-Tsuda
Rabinarayan Mishra
Benjamin Lamothe
Andreas Hoenger
Robert L Garcea
University of Colorado Boulder · USUniversity of Massachusetts Chan Medical School · US

Funding

WORKSHOPS AND TRAINING FOR IMAGE ANALYSIS USING IMODP41RR000592 · NCRR · UNIVERSITY OF COLORADO AT BOULDER · PI FELDHEIM, DAN L. · 1985 to 2011
$11.9M
MECHANISMS IN POLYOMA VIRUS ASSEMBLYR01CA037667 · NCI · UNIVERSITY OF COLORADO DENVER · PI GARCEA, ROBERT L · 1985 to 2018
$6.3M
POLYOMAVIRUS INFECTION IN IMMUNODEFICIENT MICER01CA066644 · NCI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI SZOMOLANYI-TSUDA, EVA · 1997 to 2011
$2.8M
NCI NIH HHS R01 CA037667NCI NIH HHS R01 CA066644NCI NIH HHS R01CA37667NCI NIH HHS R01CA66644NCRR NIH HHS P41 RR000592NCRR NIH HHS P41-RR000592
6 · The paper itself

Abstract

Most DNA viruses replicate in the cell nucleus, although the specific sites of virion assembly are as yet poorly defined. Electron microscopy on freeze-substituted, plastic-embedded sections of murine polyomavirus (PyV)-infected 3T3 mouse fibroblasts or mouse embryonic fibroblasts (MEFs) revealed tubular structures in the nucleus adjacent to clusters of assembled virions, with virions apparently "shed" or "budding" from their ends. Promyelocytic leukemia nuclear bodies (PML-NBs) have been suggested as possible sites for viral replication of polyomaviruses (BKV and SV40), herpes simplex virus (HSV), and adenovirus (Ad). Immunohistochemistry and FISH demonstrated co-localization of the viral T-antigen (Tag), PyV DNA, and the host DNA repair protein MRE11, adjacent to the PML-NBs. In PML⁻/⁻ MEFs the co-localization of MRE11, Tag, and PyV DNA remained unchanged, suggesting that the PML protein itself was not responsible for their association. Furthermore, PyV-infected PML⁻/⁻ MEFs and PML⁻/⁻ mice replicated wild-type levels of infectious virus. Therefore, although the PML protein may identify sites of PyV replication, neither the observed "virus factories" nor virus assembly were dependent on PML. The ultrastructure of the tubes suggests a new model for the encapsidation of small DNA viruses.

Indexed as

3T3 CellsAnimalsCell NucleusDNA-Binding ProteinsDNA Repair EnzymesDNA, ViralEmbryo, MammalianFibroblastsMiceMice, KnockoutMRE11 Homologue ProteinNuclear ProteinsPolyomavirusPolyomavirus InfectionsPromyelocytic Leukemia ProteinTranscription FactorsDNA-Binding ProteinsDNA Repair EnzymesDNA, ViralMre11a protein, mouseMRE11 Homologue ProteinNuclear ProteinsPml protein, mousePromyelocytic Leukemia ProteinTranscription FactorsTumor Suppressor Proteins

Identifiers

PMID22496654
PMCPMC3320610
OpenAlexW1971562047

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.