Evidence map›Paper›PMID 28821622›Full record

ArticleThe Journal of biological chemistry2017

The replication and transcription activator of murine gammaherpesvirus 68 cooperatively enhances cytokine-activated, STAT3-mediated gene expression.

Hui-Chen Chang Foreman, Julie Armstrong, Alexis L Santana, Laurie T Krug, Nancy C Reich

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.2field-weighted citation impact, top 41% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. 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

5 authors at 1 institution in 1 country.

Hui-Chen Chang ForemanFrom the Department of Molecular Genetics and Microbiology, Stony Brook University, Stony Brook, New York 11794.
Julie ArmstrongFrom the Department of Molecular Genetics and Microbiology, Stony Brook University, Stony Brook, New York 11794.
Alexis L SantanaFrom the Department of Molecular Genetics and Microbiology, Stony Brook University, Stony Brook, New York 11794.
Laurie T KrugFrom the Department of Molecular Genetics and Microbiology, Stony Brook University, Stony Brook, New York 11794 laurie.krug@stonybrook.edu.
Nancy C ReichFrom the Department of Molecular Genetics and Microbiology, Stony Brook University, Stony Brook, New York 11794 nancy.reich@stonybrook.edu.
Stony Brook University · US

Funding

VIRAL ONCOLOGYT32CA009176 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI HEARING, PATRICK · 1985 to 2012
$5.2M
Viral Interface with an Interferon-Induced GeneR01AI105114 · NIAID · STATE UNIVERSITY NEW YORK STONY BROOK · PI REICH MARSHALL, NANCY C. · 2014 to 2018
$2.3M
Functional Analysis of STAT3 in Gammaherpesvirus InfectionR01AI119079 · NIAID · STATE UNIVERSITY NEW YORK STONY BROOK · PI REICH MARSHALL, NANCY C. · 2015 to 2019
$2.2M
Cutaneous Biology and Skin Disease Training ProgramT32AR064184 · NIAMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ORLOW, SETH J. · 2014 to 2024
$2.1M
STAT3 Structural DeterminantsR03AI094054 · NIAID · STATE UNIVERSITY NEW YORK STONY BROOK · PI REICH MARSHALL, NANCY C. · 2011 to 2012
$157k
NCI NIH HHS T32 CA009176NIAID NIH HHS R01 AI105114NIAID NIH HHS R01 AI119079NIAID NIH HHS R03 AI094054NIAMS NIH HHS T32 AR064184
6 · The paper itself

Abstract

Gammaherpesviruses (γHVs) have a dynamic strategy for lifelong persistence, involving productive infection, latency, and intermittent reactivation. In latency reservoirs, such as B lymphocytes, γHVs exist as viral episomes and express few viral genes. Although the ability of γHV to reactivate from latency and re-enter the lytic phase is challenging to investigate and control, it is known that the γHV replication and transcription activator (RTA) can promote lytic reactivation. In this study, we provide first evidence that RTA of murine γΗV68 (MHV68) selectively binds and enhances the activity of tyrosine-phosphorylated host STAT3. STAT3 is a transcription factor classically activated by specific tyrosine 705 phosphorylation (pTyr

Indexed as

Gene Expression RegulationAmino Acid SubstitutionAnimalsB-LymphocytesCell LineDimerizationGenes, ReporterHumansImmediate-Early ProteinsInterleukin-6MiceMutationPeptide FragmentsPhosphorylationProtein Interaction Domains and MotifsProtein Processing, Post-Translationalgene 50 protein, gammaherpesvirus 68Immediate-Early ProteinsInterleukin-6Peptide FragmentsReceptors, Interleukin-6Recombinant Fusion ProteinsStat3 protein, mouseSTAT3 Transcription FactorTrans-ActivatorsTyrosinegammaherpesvirusgene expressioninfectionsignal transductionSTAT3tyrosinetyrosine phosphorylationvirology

Identifiers

PMID28821622
PMCPMC5625055
OpenAlexW2750211996

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.