Evidence map›Paper›PMID 23365434›Full record

ArticleJournal of virology2013

SMC1-mediated intra-S-phase arrest facilitates bocavirus DNA replication.

Yong Luo, Xuefeng Deng, Fang Cheng, Yi Li, Jianming Qiu

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

27 citing papers in PubMed, 43 citations in OpenAlex.

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  10. Snake venom phospholipase ACellular and molecular life sciences : CMLS · 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 2 institutions in 2 countries.

Yong LuoDepartment of Microbiology, Molecular Genetics and Immunology, University of Kansas Medical Center, Kansas City, Kansas, USA.
Xuefeng Deng
Fang Cheng
Yi Li
Jianming Qiu
University of Kansas Medical Center · USWuhan Institute of Bioengineering · CN

Funding

Novel Approaches for the Control of Microbial PathogensP30GM103326 · NIGMS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI LUTKENHAUS, JOSEPH F · 2012 to 2016
$5.3M
Post-Transcriptional Regulation of Parvovirus Capsid Gene ExpressionR01AI070723 · NIAID · UNIVERSITY OF KANSAS MEDICAL CENTER · PI QIU, JIANMING · 2007 to 2017
$3.3M
Molecular characterization of the bocavirusesR21AI085236 · NIAID · UNIVERSITY OF KANSAS MEDICAL CENTER · PI QIU, JIANMING · 2010 to 2011
$411k
Post-Transcriptional Regulation of Parvovirus Capsid Gene ExpressionR56AI070723 · NIAID · UNIVERSITY OF KANSAS MEDICAL CENTER · PI QIU, JIANMING · 2006 to 2006
$290k
NIAID NIH HHS AI070723NIAID NIH HHS AI085236NIAID NIH HHS R01 AI070723NIAID NIH HHS R21 AI085236NIAID NIH HHS R56 AI070723NIGMS NIH HHS P30 GM103326
6 · The paper itself

Abstract

Activation of a host DNA damage response (DDR) is essential for DNA replication of minute virus of canines (MVC), a member of the genus Bocavirus of the Parvoviridae family; however, the mechanism by which DDR contributes to viral DNA replication is unknown. In the current study, we demonstrate that MVC infection triggers the intra-S-phase arrest to slow down host cellular DNA replication and to recruit cellular DNA replication factors for viral DNA replication. The intra-S-phase arrest is regulated by ATM (ataxia telangiectasia-mutated kinase) signaling in a p53-independent manner. Moreover, we demonstrate that SMC1 (structural maintenance of chromosomes 1) is the key regulator of the intra-S-phase arrest induced during infection. Either knockdown of SMC1 or complementation with a dominant negative SMC1 mutant blocks both the intra-S-phase arrest and viral DNA replication. Finally, we show that the intra-S-phase arrest induced during MVC infection was caused neither by damaged host cellular DNA nor by viral proteins but by replicating viral genomes physically associated with the DNA damage sensor, the Mre11-Rad50-Nbs1 (MRN) complex. In conclusion, the feedback loop between MVC DNA replication and the intra-S-phase arrest is mediated by ATM-SMC1 signaling and plays a critical role in MVC DNA replication. Thus, our findings unravel the mechanism underlying DDR signaling-facilitated MVC DNA replication and demonstrate a novel strategy of DNA virus-host interaction.

Indexed as

AnimalsAtaxia Telangiectasia Mutated ProteinsBlotting, SouthernBocavirusBromodeoxyuridineCell Cycle CheckpointsCell Cycle ProteinsCell LineChromosomal Proteins, Non-HistoneComet AssayDNA-Binding ProteinsDNA ReplicationDogsFlow CytometryFluorescent Antibody TechniqueHost-Pathogen InteractionsAtaxia Telangiectasia Mutated ProteinsBromodeoxyuridineCell Cycle ProteinsChromosomal Proteins, Non-HistoneDNA-Binding ProteinsProtein Serine-Threonine KinasesRNA, Small InterferingStructural Maintenance of Chromosome Protein 1Tumor Suppressor Proteins

Identifiers

PMID23365434
PMCPMC3624210
OpenAlexW2084009316

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.