Evidence map›Paper›PMID 24403583›Full record

ArticleJournal of virology2014

Unconventional sequence requirement for viral late gene core promoters of murine gammaherpesvirus 68.

Elaine Wong-Ho, Ting-Ting Wu, Zoe H Davis, Bingqing Zhang, Jian Huang, Hao Gong, Hongyu Deng, Fenyong Liu, Britt Glaunsinger, Ren Sun

Open access · bronzeAbstract read
In one paragraph

Article in Journal of virology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

24 citing papers in PubMed, 36 citations in OpenAlex.

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  7. Conserved CxJournal of virology · 2020
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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

10 authors at 4 institutions in 2 countries.

Elaine Wong-HoDepartment of Molecular & Medical Pharmacology,University of California at Los Angeles, Los Angeles, California, USA.
Ting-Ting Wu
Zoe H Davis
Bingqing Zhang
Jian Huang
Hao Gong
Hongyu Deng
Fenyong Liu
Britt Glaunsinger
Ren Sun
University of California, Berkeley · USUniversity of California, Los Angeles · USSecond Affiliated Hospital of Zhejiang University · CNChinese Academy of Sciences · CN

Funding

Women's CancersP30CA016042 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI Samuel Wheeler French · 1985 to 2026
$134.5M
Disruption of Cellular RNA Processing by Kaposi's Sarcoma-Associated HerpesvirusR01CA136367 · NCI · UNIVERSITY OF CALIFORNIA BERKELEY · PI Britt A Glaunsinger · 2010 to 2026
$5.8M
Reactivation of Kaposi's Sarcoma-Associated HerpesvirusR01CA091791 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SUN, REN · 2001 to 2017
$4.4M
Role of Interleukin-6 in Gammaherpesvirus replicationR01DE015752 · NIDCR · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SUN, REN · 2003 to 2007
$1.6M
Escape from gammaherpesvirus-induced mRNA destructionR01CA160556 · NCI · UNIVERSITY OF CALIFORNIA BERKELEY · PI GLAUNSINGER, BRITT A · 2011 to 2015
$1.5M
Quantitative High-Resolution Genetic Profiling of a GammaherpesvirusR21AI078133 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI SUN, REN · 2010 to 2011
$422k
NCI NIH HHS CA136367NCI NIH HHS CA160556NCI NIH HHS CA91791NCI NIH HHS P30 CA016042NCI NIH HHS R01 CA091791NCI NIH HHS R01 CA136367NCI NIH HHS R01 CA160556NIAID NIH HHS AI078133NIAID NIH HHS R21 AI078133NIDCR NIH HHS DE15752NIDCR NIH HHS R01 DE015752
6 · The paper itself

Abstract

Infection with the human gammaherpesviruses, Epstein-Barr virus (EBV) and Kaposi's sarcoma-associated herpesvirus (KSHV), is associated with several cancers. During lytic replication of herpesviruses, viral genes are expressed in an ordered cascade. However, the mechanism by which late gene expression is regulated has not been well characterized in gammaherpesviruses. In this study, we have investigated the cis element that mediates late gene expression during de novo lytic infection with murine gammaherpesvirus 68 (MHV-68). A reporter system was established and used to assess the activity of viral late gene promoters upon infection with MHV-68. It was found that the viral origin of lytic replication, orilyt, must be on the reporter plasmid to support activation of the late gene promoter. Furthermore, the DNA sequence required for the activation of late gene promoters was mapped to a core element containing a distinct TATT box and its neighboring sequences. The critical nucleotides of the TATT box region were determined by systematic mutagenesis in the reporter system, and the significance of these nucleotides was confirmed in the context of the viral genome. In addition, EBV and KSHV late gene core promoters could be activated by MHV-68 lytic replication, indicating that the mechanisms controlling late gene expression are conserved among gammaherpesviruses. Therefore, our results on MHV-68 establish a solid foundation for mechanistic studies of late gene regulation.

Indexed as

Promoter Regions, GeneticTranscription, GeneticAnimalsBase SequenceGene Expression Regulation, ViralHerpesviridae InfectionsMiceMolecular Sequence DataReplication OriginRhadinovirusRodent DiseasesTATA BoxViral ProteinsVirus ReplicationViral Proteins

Identifiers

PMID24403583
PMCPMC3957950
OpenAlexW2007981773

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.