Evidence map›Paper›PMID 33674350›Full record

ArticleGenome research2021

AP-1 subunits converge promiscuously at enhancers to potentiate transcription.

Jungkyun Seo, D Dewran Koçak, Luke C Bartelt, Courtney A Williams, Alejandro Barrera, Charles A Gersbach, Timothy E Reddy

Open access · bronzeAbstract read
In one paragraph

Article in Genome research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
–field-weighted citation impact
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

32 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. The Encyclopedia of DNA Elements.bioRxiv : the preprint server for biology · 2026
    Article
  6. Review
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  9. Regulatory dynamics ofLupus science & medicine · 2026
    Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Context dependent activity of p63-bound gene regulatory elements.bioRxiv : the preprint server for biology · 2024
    Article
  20. GermlineeLife · 2024
    Article
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

7 authors at 1 institution in 2 countries.

Jungkyun Seo *Department of Biostatistics and Bioinformatics, Division of Integrative Genomics, Duke University Medical Center, Durham, North Carolina 27708, USA.ORCID 0000-0001-5514-4421
D Dewran Koçak *Center for Genomic and Computational Biology, Duke University, Durham, North Carolina 27708, USA.
Luke C BarteltCenter for Genomic and Computational Biology, Duke University, Durham, North Carolina 27708, USA.
Courtney A WilliamsCenter for Genomic and Computational Biology, Duke University, Durham, North Carolina 27708, USA.
Alejandro BarreraDepartment of Biostatistics and Bioinformatics, Division of Integrative Genomics, Duke University Medical Center, Durham, North Carolina 27708, USA.
Charles A GersbachComputational Biology and Bioinformatics Graduate Program, Duke University, Durham, North Carolina 27708, USA.
Timothy E ReddyDepartment of Biostatistics and Bioinformatics, Division of Integrative Genomics, Duke University Medical Center, Durham, North Carolina 27708, USA.
Duke University · US

Funding

Decoding and Reprogramming the Corticosteroid Transcriptional Regulatory NetworkU01HG007900 · NHGRI · DUKE UNIVERSITY · PI REDDY, TIMOTHY E · 2015 to 2017
$5.9M
Quantifying the genetic diversity of human regulatory element activityR01HG010741 · NHGRI · DUKE UNIVERSITY · PI ALLEN, ANDREW S, CRAWFORD, GREGORY E · 2019 to 2022
$3.1M
Engineering Targeted Epigenetic Modifiers for Precise Control of Gene RegulationR01DA036865 · NIDA · DUKE UNIVERSITY · PI CRAWFORD, GREGORY E, GERSBACH, CHARLES A. · 2013 to 2017
$2.6M
NHGRI NIH HHS R01 HG010741NHGRI NIH HHS U01 HG007900NIDA NIH HHS R01 DA036865
6 · The paper itself

Abstract

The AP-1 transcription factor (TF) dimer contributes to many biological processes and environmental responses. AP-1 can be composed of many interchangeable subunits. Unambiguously determining the binding locations of these subunits in the human genome is challenging because of variable antibody specificity and affinity. Here, we definitively establish the genome-wide binding patterns of five AP-1 subunits by using CRISPR to introduce a common antibody tag on each subunit. We find limited evidence for strong dimerization preferences between subunits at steady state and find that, under a stimulus, dimerization patterns reflect changes in the transcriptome. Further, our analysis suggests that canonical AP-1 motifs indiscriminately recruit all AP-1 subunits to genomic sites, which we term AP-1 hotspots. We find that AP-1 hotspots are predictive of cell type-specific gene expression and of genomic responses to glucocorticoid signaling (more so than super-enhancers) and are significantly enriched in disease-associated genetic variants. Together, these results support a model where promiscuous binding of many AP-1 subunits to the same genomic location play a key role in regulating cell type-specific gene expression and environmental responses.

Indexed as

Enhancer Elements, GeneticGene Expression RegulationTranscription, GeneticHumansSignal TransductionTranscription Factor AP-1Transcription Factor AP-1

Identifiers

PMID33674350
PMCPMC8015846
OpenAlexW3135152445

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.