Evidence map›Paper›PMID 36395771›Full record

ArticleMolecular cell2022

PAX3-FOXO1 coordinates enhancer architecture, eRNA transcription, and RNA polymerase pause release at select gene targets.

Susu Zhang, Jing Wang, Qi Liu, W Hayes McDonald, Monica L Bomber, Hillary M Layden, Jacob Ellis, Scott C Borinstein, Scott W Hiebert, Kristy R Stengel

Open access · greenAbstract read
In one paragraph

Article in Molecular cell, 2022. 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
2.7field-weighted citation impact, top 9% 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

32 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
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  7. Metabolic Reprogramming Driven by Trophoblasts and Decidual XCR1Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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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

10 authors at 2 institutions in 1 country.

Susu ZhangDepartment of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
Jing WangDepartment of Biostatistics, Vanderbilt University School of Medicine, Nashville, TN 37203, USA; Center for Quantitative Sciences, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Qi LiuDepartment of Biostatistics, Vanderbilt University School of Medicine, Nashville, TN 37203, USA; Center for Quantitative Sciences, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
W Hayes McDonaldDepartment of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
Monica L BomberDepartment of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
Hillary M LaydenDepartment of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
Jacob EllisDepartment of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.
Scott C BorinsteinDepartment of Pediatrics, Vanderbilt University School of Medicine, Vanderbilt University Medical Center, Nashville, TN 37203, USA; Vanderbilt-Ingram Cancer Center, Nashville, TN 37027, USA.
Scott W HiebertDepartment of Biochemistry, Vanderbilt University School of Medicine, Nashville, TN 37232, USA; Vanderbilt-Ingram Cancer Center, Nashville, TN 37027, USA. Electronic address: scott.hiebert@vanderbilt.edu.
Kristy R StengelDepartment of Cell Biology, Albert Einstein College of Medicine, New York, NY, USA; Montefiore Einstein Cancer Center, Albert Einstein College of Medicine, New York, NY, USA. Electronic address: kristy.stengel@einsteinmed.edu.
Vanderbilt University · USAlbert Einstein College of Medicine · US

Funding

Tumor Immunology and Microenvironment Research ProgramP30CA068485 · NCI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI STACIE B DUSETZINA · 1995 to 2026
$172.8M
The Vanderbilt Institute for Clinical and Translational Research (VICTR)UL1TR000445 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BERNARD, GORDON RAPHAEL · 2012 to 2016
$41.4M
Translational Analysis CoreP30DK058404 · NIDDK · VANDERBILT UNIVERSITY MEDICAL CENTER · PI RICHARD M. PEEK · 2002 to 2026
$29.9M
BIOCHEMICAL &CHEMICAL TRAINING FOR CANCER RESEARCHT32CA009582 · NCI · VANDERBILT UNIVERSITY · PI David K Cortez · 1987 to 2026
$8.8M
Hdac3 as a therapeutic target in BCL6-dependent lymphomaR01CA164605 · NCI · VANDERBILT UNIVERSITY · PI HIEBERT, SCOTT W · 2012 to 2022
$3.9M
Role of PRC1 in RUNX1-ETO-mediated transcriptional controlR01CA255446 · NCI · VANDERBILT UNIVERSITY · PI HODGES, EMILY · 2021 to 2025
$2.1M
CRISPR-mediated Chemical Genetics Define Transcription Factor Gene Networks and Mechanisms of ControlR35GM147213 · NIGMS · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI Kristy Stengel · 2022 to 2026
$2.1M
Determining the role of WT and mutant FOXO1 in the transcriptional regulation of DLBCLF31HL156565 · NHLBI · VANDERBILT UNIVERSITY · PI LAYDEN, HILLARY MARGARET · 2021 to 2023
$96k
NCATS NIH HHS UL1 TR000445NCI NIH HHS P30 CA068485NCI NIH HHS R01 CA164605NCI NIH HHS R01 CA255446NCI NIH HHS T32 CA009582NHLBI NIH HHS F31 HL156565NIDDK NIH HHS P30 DK058404NIGMS NIH HHS R35 GM147213
6 · The paper itself

Abstract

Transcriptional control is a highly dynamic process that changes rapidly in response to various cellular and extracellular cues, making it difficult to define the mechanism of transcription factor function using slow genetic methods. We used a chemical-genetic approach to rapidly degrade a canonical transcriptional activator, PAX3-FOXO1, to define the mechanism by which it regulates gene expression programs. By coupling rapid protein degradation with the analysis of nascent transcription over short time courses and integrating CUT&RUN, ATAC-seq, and eRNA analysis with deep proteomic analysis, we defined PAX3-FOXO1 function at a small network of direct transcriptional targets. PAX3-FOXO1 degradation impaired RNA polymerase pause release and transcription elongation at most regulated gene targets. Moreover, the activity of PAX3-FOXO1 at enhancers controlling this core network was surprisingly selective, affecting single elements in super-enhancers. This combinatorial analysis indicated that PAX3-FOXO1 was continuously required to maintain chromatin accessibility and enhancer architecture at regulated enhancers.

Indexed as

ProteomicsRegulatory Sequences, Nucleic AcidBase SequenceChromatin Immunoprecipitation SequencingDNA-Directed RNA PolymerasesTranscription FactorsDNA-Directed RNA PolymerasesTranscription FactorsATAC-seqchromatin remodelingdifferentiationenhancerPAX3PAX3-FOXO1PRO-seqrhabdomyosarcomat(2;13)(q35;q14)therapeutics

Identifiers

PMID36395771
PMCPMC9731406
OpenAlexW4309341173

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.