Evidence map›Paper›PMID 23087374›Full record

ArticleNucleic acids research2013

The BET bromodomain inhibitor JQ1 activates HIV latency through antagonizing Brd4 inhibition of Tat-transactivation.

Zichong Li, Jia Guo, Yuntao Wu, Qiang Zhou

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 205 papers.

0numbers the graph read from it
0cells of the map it votes in
205citing papers in PubMed
8.3field-weighted citation impact, top 2% 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

205 citing papers in PubMed, 302 citations in OpenAlex.

  1. Article
  2. Review
  3. Structural basis for P-TEFb association with BRD4.bioRxiv : the preprint server for biology · 2026
    Article
  4. Review
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  12. Article
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  14. Article
  15. Article
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  17. Article
  18. BRD9 functions as an HIV-1 latency regulatory factor.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  19. Article
  20. Article

145 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

4 authors at 2 institutions in 1 country.

Zichong LiDepartment of Molecular and Cell Biology, University of California, Berkeley, CA 94720, USA.
Jia Guo
Yuntao Wu
Qiang Zhou
George Mason University · USUniversity of California, Berkeley · US

Funding

REGULATION OF TRANSCRIPTIONAL ELONGATION BY HIV1 TATR01AI041757 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI ZHOU, QIANG · 1997 to 2019
$6.6M
Tat cofactors and control of HIV-1 latencyR01AI095057 · NIAID · UNIVERSITY OF CALIFORNIA BERKELEY · PI ZHOU, QIANG · 2011 to 2015
$1.9M
Regulation of Cofilin in HIV-1 Infection of Human CD4 T CellsR01AI081568 · NIAID · GEORGE MASON UNIVERSITY · PI WU, YUNTAO · 2009 to 2012
$1.2M
NIAID NIH HHS R01AI081568NIAID NIH HHS R01 AI095057NIAID NIH HHS R01AI095057NIAID NIH HHS R01AI41757
6 · The paper itself

Abstract

Latent HIV reservoirs are the primary hurdle to eradication of infection. Identification of agents, pathways and molecular mechanisms that activate latent provirus may, in the presence of highly active antiretroviral therapy, permit clearance of infected cells by the immune system. Promoter-proximal pausing of RNA polymerase (Pol) II is a major rate-limiting step in HIV gene expression. The viral Tat protein recruits human Super Elongation Complex (SEC) to paused Pol II to overcome this limitation. Here, we identify the bromodomain protein Brd4 and its inhibition of Tat-transactivation as a major impediment to latency reactivation. Brd4 competitively blocks the Tat-SEC interaction on HIV promoter. The BET bromodomain inhibitor JQ1 dissociates Brd4 from the HIV promoter to allow Tat recruitment of SEC to stimulate HIV elongation. JQ1 synergizes with another latency activator prostratin, which promotes Pol II loading onto the viral promoter. Because JQ1 activates viral latency without inducing global T cell activation, this and other closely related compounds and their antagonization of Brd4 to promote Tat-SEC interaction merit further investigations as effective agents/strategies for eliminating latent HIV.

Indexed as

Anti-HIV AgentsAzepinesBromodomain Containing ProteinsCell Cycle ProteinsCyclin-Dependent Kinase 9HeLa CellsHIVHumansJurkat CellsNuclear ProteinsPhorbol EstersPhosphorylationPositive Transcriptional Elongation Factor BPromoter Regions, GeneticRibonucleoproteins, Small NuclearRNA Polymerase IIAnti-HIV AgentsAzepinesBRD4 protein, humanBromodomain Containing ProteinsCell Cycle ProteinsCyclin-Dependent Kinase 9ELL2 protein, human(+)-JQ1 compoundNuclear ProteinsPhorbol EstersPositive Transcriptional Elongation Factor BprostratinRibonucleoproteins, Small NuclearRNA Polymerase IItat Gene Products, Human Immunodeficiency VirusTranscriptional Elongation FactorsTranscription FactorsTriazoles

Identifiers

PMID23087374
PMCPMC3592394
OpenAlexW2103409409

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.