Evidence map›Paper›PMID 21507979›Full record

ArticleJournal of virology2011

The single RBP-Jkappa site within the LANA promoter is crucial for establishing Kaposi's sarcoma-associated herpesvirus latency during primary infection.

Jie Lu, Subhash C Verma, Qiliang Cai, Erle S Robertson

Abstract read
In one paragraph

Article in Journal of virology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

26 citing papers in PubMed, 33 citations in OpenAlex.

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  19. Epigenetic regulation of EBV and KSHV latency.Current opinion in virology · 2013
    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

4 authors at 2 institutions in 1 country.

Jie LuDepartment of Microbiology and, Tumor Virology Program of the Abramson Comprehensive Cancer Center, University of Pennsylvania, School of Medicine, 201E Johnson Pavilion, 3610 Hamilton Walk, Philadelphia, PA 19104, USA.
Subhash C Verma
Qiliang Cai
Erle S Robertson
University of Pennsylvania · USUniversity of Nevada, Reno · US

Funding

Mechanisms of Action of LANA encoded by KSHVR01CA091792 · NCI · UNIVERSITY OF PENNSYLVANIA · PI ROBERTSON, ERLE S. · 2002 to 2011
$3.4M
Mechanism of KSHV reactivationR01DE017338 · NIDCR · UNIVERSITY OF PENNSYLVANIA · PI ROBERTSON, ERLE S · 2005 to 2007
$811k
Understanding the mechanism of KSHV latent DNA replicationR00CA126182 · NCI · UNIVERSITY OF NEVADA RENO · PI VERMA, SUBHASH C · 2009 to 2011
$740k
Understanding the mechanism of KSHV latent DNA replicationK99CA126182 · NCI · UNIVERSITY OF PENNSYLVANIA · PI VERMA, SUBHASH C · 2007 to 2008
$250k
NCI NIH HHS CA072510NCI NIH HHS CA091792NCI NIH HHS K99 CA126182NCI NIH HHS K99CA126182NCI NIH HHS R00 CA126182NCI NIH HHS R01 CA091792NIDCR NIH HHS DE017338NIDCR NIH HHS R01 DE017338
6 · The paper itself

Abstract

Kaposi's sarcoma-associated herpesvirus (KSHV; or human herpesvirus 8 [HHV8]) is implicated in the pathogenesis of many human malignancies including Kaposi's sarcoma (KS), multicentric Castleman's disease (MCD), and primary effusion lymphoma (PEL). KSHV infection displays two alternative life cycles, referred to as the latent and lytic or productive cycle. Previously, we have reported that the replication and transcription activator (RTA), a major lytic cycle transactivator, contributes to the development of KSHV latency by inducing latency-associated nuclear antigen (LANA) expression during early stages of infection by targeting RBP-Jκ, the master regulator of the Notch signaling pathway. Here, we generated a bacterial artificial chromosome (BAC) KSHV recombinant virus with a deletion of the RBP-Jκ site within the LANA promoter to evaluate the function of the RBP-Jκ cognate site in establishing primary latent infection. The results showed that genetic disruption of the RBP-Jκ binding site within the KSHV LANA promoter led to enhanced expression of the KSHV-encoded immediate early RTA, resulting in an increase in lytic replication during primary infection of human peripheral blood mononuclear cells (PBMCs). This system provides a powerful tool for use in indentifying additional cellular and viral molecules involved in LANA-mediated latency maintenance during the early stages of KSHV infection.

Indexed as

Virus LatencyAntigens, ViralBinding SitesCell LineChromosomes, Artificial, BacterialGene Expression Regulation, ViralHerpesvirus 8, HumanHumansImmediate-Early ProteinsImmunoglobulin J Recombination Signal Sequence-Binding ProteinLeukocytes, MononuclearNuclear ProteinsPromoter Regions, GeneticRecombination, GeneticTrans-ActivatorsVirus ActivationAntigens, ViralImmediate-Early ProteinsImmunoglobulin J Recombination Signal Sequence-Binding Proteinlatency-associated nuclear antigenNuclear ProteinsRBPJ protein, humanRta protein, Human herpesvirus 8Trans-Activators

Identifiers

PMID21507979
PMCPMC3126528
OpenAlexW2060521646

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.