Evidence map›Paper›PMID 40695292›Full record

ArticleMolecular cell2025

β-catenin functions as a molecular adapter for disordered cBAF interactions.

Yuen San Chan, Qinyu Gao, Sarah A Robinson, Wenzhi Wang, Ruzena Filandrova, Lisa-Maria Weinhold, Mario Loeza Cabrera, Miao Zhang, Chandra Shekar R Ambati, Antonio M Lerario and 8 more

Abstract read
In one paragraph

Article in Molecular cell, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Distinct Transcriptional Programs Controlled byMedical sciences (Basel, Switzerland) · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Characterization ofBiomolecules · 2026
    Article
  6. Phase separation and the tumor microenvironment.Cell communication and signaling : CCS · 2026
    Review
  7. 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

18 authors.

Yuen San ChanDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA; Center for Precision Environmental Health, Baylor College of Medicine, Houston, TX 77030, USA.
Qinyu GaoDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA; Center for Precision Environmental Health, Baylor College of Medicine, Houston, TX 77030, USA.
Sarah A RobinsonDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA; Center for Precision Environmental Health, Baylor College of Medicine, Houston, TX 77030, USA.
Wenzhi WangDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA; Center for Precision Environmental Health, Baylor College of Medicine, Houston, TX 77030, USA.
Ruzena FilandrovaInstitute of Organic Chemistry and Biochemistry, Czech Academy of Sciences, Prague, Czech Republic.
Lisa-Maria WeinholdInstitute of Organic Chemistry and Biochemistry, Czech Academy of Sciences, Prague, Czech Republic; Department of Cell Biology, Faculty of Science, Charles University, Prague, Czech Republic.
Mario Loeza CabreraDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA; Center for Precision Environmental Health, Baylor College of Medicine, Houston, TX 77030, USA.
Miao ZhangDepartment of Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Chandra Shekar R AmbatiAdvanced Technology Cores, Baylor College of Medicine, Houston, TX 77030, USA.
Antonio M LerarioDepartment of Internal Medicine, Division of Metabolism, Endocrinology and Diabetes, University of Michigan, Ann Arbor, MI 48105, USA.
Nagireddy PutluriDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA; Advanced Technology Cores, Baylor College of Medicine, Houston, TX 77030, USA; Dan L Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX 77030, USA.
Katja Kiseljak-VassiliadesDivision of Endocrinology, Metabolism and Diabetes, Department of Medicine, University of Colorado School of Medicine at Colorado Anschutz Medical Campus, Aurora, CO 80045, USA; Research Service Rocky Mountain Regional Veterans Affairs Medical Center, Aurora, CO 80045, USA.
Margaret E WiermanDivision of Endocrinology, Metabolism and Diabetes, Department of Medicine, University of Colorado School of Medicine at Colorado Anschutz Medical Campus, Aurora, CO 80045, USA; Research Service Rocky Mountain Regional Veterans Affairs Medical Center, Aurora, CO 80045, USA.
Mouhammed Amir HabraDepartment of Endocrine Neoplasia and Hormonal Disorders, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.
Gary D HammerDepartment of Internal Medicine, Division of Metabolism, Endocrinology and Diabetes, University of Michigan, Ann Arbor, MI 48105, USA; Endocrine Oncology Program, Rogel Cancer Center, University of Michigan Health System, Ann Arbor, MI 48109, USA.
Vaclav VeverkaInstitute of Organic Chemistry and Biochemistry, Czech Academy of Sciences, Prague, Czech Republic; Department of Cell Biology, Faculty of Science, Charles University, Prague, Czech Republic.
Katerina CermakovaCenter for Precision Environmental Health, Baylor College of Medicine, Houston, TX 77030, USA; Department of Biochemistry and Molecular Pharmacology, Baylor College of Medicine, Houston, TX 77030, USA. Electronic address: katerina.cermakova@bcm.edu.
H Courtney HodgesDepartment of Molecular and Cellular Biology, Baylor College of Medicine, Houston, TX 77030, USA; Center for Precision Environmental Health, Baylor College of Medicine, Houston, TX 77030, USA; Dan L Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX 77030, USA; Department of Bioengineering, Rice University, Houston, TX 77030, USA. Electronic address: chodges@bcm.edu.

Funding

Tumor BiologyP30CA125123 · NCI · BAYLOR COLLEGE OF MEDICINE · PI Suzanne AW Fuqua · 2007 to 2026
$73.9M
Novel cellular regulatory mechanisms governing SWI/SNF activityR35GM137996 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI Hamilton Courtney Hodges · 2020 to 2026
$2.9M
Mechanisms and small-molecule targeting of SWI/SNF activity in neuroblastomaR01CA272769 · NCI · BAYLOR COLLEGE OF MEDICINE · PI Hamilton Courtney Hodges · 2022 to 2026
$2.3M
Racial Disparity in Bladder Cancer and Identification of Altered Metabolism in African American Compare to European Bladder CancerR01CA220297 · NCI · BAYLOR COLLEGE OF MEDICINE · PI PUTLURI, NAGIREDDY · 2017 to 2021
$1.8M
NCI NIH HHS P30 CA125123NCI NIH HHS R01 CA220297NCI NIH HHS R01 CA272769NIGMS NIH HHS R35 GM137996
6 · The paper itself

Abstract

BAF (SWI/SNF) chromatin remodelers engage binding partners to generate site-specific DNA accessibility. However, the basis for interaction between BAF and divergent binding partners has remained unclear. Here, we tested the hypothesis that scaffold proteins augment BAF's binding repertoire by examining β-catenin (CTNNB1) and steroidogenic factor 1 (SF-1, NR5A1), a transcription factor central to steroid production in human cells. BAF inhibition rapidly opposed SF-1/β-catenin enhancer occupancy, impairing SF-1 target activation and SF-1/β-catenin autoregulation. These effects arise due to β-catenin's role as a molecular adapter between SF-1 and an intrinsically disordered region (IDR) of the canonical BAF (cBAF) subunit ARID1A. In contrast to exclusively IDR-driven mechanisms, adapter function is mediated by direct association of ARID1A with β-catenin's folded Armadillo repeats. β-catenin similarly linked cBAF to YAP1, SOX2, FOXO3, and CBP/p300, reflecting a general IDR-mediated mechanism for modular coordination between factors. Molecular visualization highlights β-catenin's adapter role for interaction of cBAF with binding partners.

Indexed as

beta CateninDNA-Binding ProteinsIntrinsically Disordered ProteinsNuclear ProteinsSteroidogenic Factor 1Transcription FactorsAdaptor Proteins, Signal TransducingBinding SitesEnhancer Elements, GeneticForkhead Box Protein O3HEK293 CellsHumansp300-CBP Transcription FactorsPhosphoproteinsProtein BindingSignal TransductionAdaptor Proteins, Signal TransducingARID1A protein, humanbeta CateninCTNNB1 protein, humanDNA-Binding ProteinsForkhead Box Protein O3Intrinsically Disordered ProteinsNR5A1 protein, humanNuclear Proteinsp300-CBP Transcription FactorsPhosphoproteinsSteroidogenic Factor 1Transcription FactorsYAP1 protein, humanYAP-Signaling Proteinsadrenocortical carcinomachromatin remodelingco-activatorsIDRsscaffold proteinssteroid hormonestranscription factorstranscription regulatorsunstructured protein

Identifiers

PMID40695292
PMCPMC12323811

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Registered trials

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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.