Evidence map›Paper›PMID 27414498›Full record

ArticleCell host & microbe2016

Toxoplasma Effector Recruits the Mi-2/NuRD Complex to Repress STAT1 Transcription and Block IFN-γ-Dependent Gene Expression.

Philipp Olias, Ronald D Etheridge, Yong Zhang, Michael J Holtzman, L David Sibley

Open access · bronzeAbstract read
In one paragraph

Article in Cell host & microbe, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 108 papers.

0numbers the graph read from it
0cells of the map it votes in
108citing papers in PubMed
14.4field-weighted citation impact, top 1% 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

108 citing papers in PubMed, 185 citations in OpenAlex.

  1. Review
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  14. Proceedings of the National Academy of Sciences of the United States of America · 2025
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  16. NcROP2 deletion reducesFrontiers in immunology · 2025
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  17. Molecular interactions ofFrontiers in veterinary science · 2025
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48 more citing papers are in PubMed but not listed here.

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.

Philipp OliasDepartment of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Ronald D EtheridgeDepartment of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Yong ZhangDepartment of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
Michael J HoltzmanDepartment of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
L David SibleyDepartment of Molecular Microbiology, Washington University School of Medicine, St. Louis, MO 63110, USA. Electronic address: sibley@wustl.edu.
Washington University in St. Louis · US

Funding

Tissue and Cell Processing CoreU19AI070489 · NIAID · WASHINGTON UNIVERSITY · PI HOLTZMAN, MICHAEL J · 2006 to 2016
$17.9M
Molecular Basis of Human ToxoplasmosisR01AI118426 · NIAID · WASHINGTON UNIVERSITY · PI SIBLEY, L. DAVID · 2015 to 2024
$6.0M
MOLECULAR BASIS OF TOXOPLASMOSIS IN AIDS PATIENTSR01AI036629 · NIAID · WASHINGTON UNIVERSITY · PI SIBLEY, L. DAVID · 1994 to 2013
$5.3M
PARP9-DTX3L Control Of Viral Infection and Airway DiseaseR01AI130591 · NIAID · WASHINGTON UNIVERSITY · PI HOLTZMAN, MICHAEL J · 2017 to 2021
$3.0M
INTERFERON SIGNAL ENHANCERS AS ANTIVIRAL THERAPEUTICSR01AI111605 · NIAID · WASHINGTON UNIVERSITY · PI HOLTZMAN, MICHAEL J · 2014 to 2017
$1.8M
NIAID NIH HHS R01 AI036629NIAID NIH HHS R01 AI111605NIAID NIH HHS R01 AI118426NIAID NIH HHS R01 AI130591NIAID NIH HHS U19 AI070489
6 · The paper itself

Abstract

Interferon gamma (IFN-γ) is an essential mediator of host defense against intracellular pathogens, including the protozoan parasite Toxoplasma gondii. However, prior T. gondii infection blocks IFN-γ-dependent gene transcription, despite the downstream transcriptional activator STAT1 being activated and bound to cognate nuclear promoters. We identify the parasite effector that blocks STAT1-dependent transcription and show it is associated with recruitment of the Mi-2 nucleosome remodeling and deacetylase (NuRD) complex, a chromatin-modifying repressor. This secreted effector, toxoplasma inhibitor of STAT1-dependent transcription (TgIST), translocates to the host cell nucleus, where it recruits Mi-2/NuRD to STAT1-dependent promoters, resulting in altered chromatin and blocked transcription. TgIST is conserved across strains, underlying their shared ability to block IFN-γ-dependent transcription. TgIST deletion results in increased parasite clearance in IFN-γ-activated cells and reduced mouse virulence, which is restored in IFN-γ-receptor-deficient mice. These findings demonstrate the importance of both IFN-γ responses and the ability of pathogens to counteract these defenses.

Indexed as

Host-Pathogen InteractionsImmune EvasionAnimalsGene DeletionInterferon-gammaMi-2 Nucleosome Remodeling and Deacetylase ComplexMiceProtozoan ProteinsSTAT1 Transcription FactorToxoplasmaTranscription, GeneticIFNG protein, mouseInterferon-gammaMi-2 Nucleosome Remodeling and Deacetylase ComplexProtozoan ProteinsStat1 protein, mouseSTAT1 Transcription Factoracetylationnuclear transportphosphorylationsignalingtranscription

Identifiers

PMID27414498
PMCPMC4947229
OpenAlexW2478664567

What OpenQuestion holds

Textmetadata
LicenceTDM
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.