Evidence map›Paper›PMID 22319441›Full record

ArticlePLoS pathogens2012

Viral cyclins mediate separate phases of infection by integrating functions of distinct mammalian cyclins.

Katherine S Lee, Andrea L Suarez, David J Claypool, Taylor K Armstrong, Erin M Buckingham, Linda F van Dyk

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 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

14 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Host Tumor Suppressor p18Journal of virology · 2018
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
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

6 authors at 2 institutions in 1 country.

Katherine S LeeDepartment of Microbiology, University of Colorado Denver, Anschutz Medical Campus, Aurora, Colorado, USA.
Andrea L Suarez
David J Claypool
Taylor K Armstrong
Erin M Buckingham
Linda F van Dyk
University of Colorado Denver · USUniversity of Colorado Anschutz Medical Campus · US

Funding

TRAINING PROGRAM IN IMMUNOLOGYT32AI007405 · NIAID · UNIVERSITY OF COLORADO DENVER · PI Laurel L Lenz, Raul Martin Torres · 1991 to 2026
$10.5M
Predoctoral Training Program in Molecular BiologyT32GM008730 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI PREKERIS, RYTIS, SCLAFANI, ROBERT A · 1999 to 2019
$3.3M
Molecular Pathogenesis of Infectious DiseasesT32AI052066 · NIAID · UNIVERSITY OF COLORADO DENVER · PI VAN DYK, LINDA F. · 2002 to 2022
$2.3M
In Vivo Analysis of Viral CyclinR01CA103632 · NCI · UNIVERSITY OF COLORADO DENVER · PI VAN DYK, LINDA F. · 2004 to 2008
$1.4M
Molecular Basis of Microbial PathogenesisT32AI007537 · NIAID · UNIVERSITY OF COLORADO DENVER · PI HOLMES, RANDALL K · 1998 to 2007
$1.3M
Characterization of an animal model of chronic infection and diseaseR03AI082490 · NIAID · UNIVERSITY OF COLORADO DENVER · PI VAN DYK, LINDA F. · 2009 to 2010
$154k
Cell Type Specific Outcomes of Gammaherpesvirus Infection.F31CA132561 · NCI · UNIVERSITY OF COLORADO DENVER · PI SUAREZ, ANDREA · 2007 to 2009
$34k
NCI NIH HHS F31 CA132561NCI NIH HHS F31 CA132561-01NCI NIH HHS R01 CA103632NIAID NIH HHS R03 AI082490NIAID NIH HHS T32 AI007405NIAID NIH HHS T32 AI007405-18NIAID NIH HHS T32 AI007537NIAID NIH HHS T32 AI052066NIAID NIH HHS T32 AI07537-09NIAID NIH HHS T32 AI52066-02NIGMS NIH HHS T32 GM008730NIGMS NIH HHS T32 GM08730
6 · The paper itself

Abstract

Gammaherpesvirus cyclins have expanded biochemical features relative to mammalian cyclins, and promote infection and pathogenesis including acute lung infection, viral persistence, and reactivation from latency. To define the essential features of the viral cyclin, we generated a panel of knock-in viruses expressing various viral or mammalian cyclins from the murine gammaherpesvirus 68 cyclin locus. Viral cyclins of both gammaherpesvirus 68 and Kaposi's sarcoma-associated herpesvirus supported all cyclin-dependent stages of infection, indicating functional conservation. Although mammalian cyclins could not restore lung replication, they did promote viral persistence and reactivation. Strikingly, distinct and non-overlapping mammalian cyclins complemented persistence (cyclin A, E) or reactivation from latency (cyclin D3). Based on these data, unique biochemical features of viral cyclins (e.g. enhanced kinase activation) are not essential to mediate specific processes during infection. What is essential for, and unique to, the viral cyclins is the integration of the activities of several different mammalian cyclins, which allows viral cyclins to mediate multiple, discrete stages of infection. These studies also demonstrated that closely related stages of infection, that are cyclin-dependent, are in fact genetically distinct, and thus predict that cyclin requirements may be used to tailor potential therapies for virus-associated diseases.

Indexed as

AnimalsCyclinsGammaherpesvirinaeGene Expression Regulation, ViralHerpesviridae InfectionsMiceMice, Inbred BALB CMice, Inbred C57BLViral ProteinsVirus ActivationVirus ReplicationCyclinsViral Proteins

Identifiers

PMID22319441
PMCPMC3271081
OpenAlexW1982312026

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.