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

Mol Cell. 2025 Aug 21;85(16):3041-3056.e9. doi: 10.1016/j.molcel.2025.06.026. Epub 2025 Jul 21.

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.

Keywords: IDRs; adrenocortical carcinoma; chromatin remodeling; co-activators; scaffold proteins; steroid hormones; transcription factors; transcription regulators; unstructured protein.

MeSH terms

  • Adaptor Proteins, Signal Transducing / genetics
  • Adaptor Proteins, Signal Transducing / metabolism
  • Binding Sites
  • DNA-Binding Proteins* / chemistry
  • DNA-Binding Proteins* / genetics
  • DNA-Binding Proteins* / metabolism
  • Enhancer Elements, Genetic
  • Forkhead Box Protein O3 / genetics
  • Forkhead Box Protein O3 / metabolism
  • HEK293 Cells
  • Humans
  • Intrinsically Disordered Proteins* / genetics
  • Intrinsically Disordered Proteins* / metabolism
  • Nuclear Proteins* / genetics
  • Nuclear Proteins* / metabolism
  • Phosphoproteins / genetics
  • Phosphoproteins / metabolism
  • Protein Binding
  • Signal Transduction
  • Steroidogenic Factor 1* / genetics
  • Steroidogenic Factor 1* / metabolism
  • Transcription Factors* / chemistry
  • Transcription Factors* / genetics
  • Transcription Factors* / metabolism
  • YAP-Signaling Proteins
  • beta Catenin* / chemistry
  • beta Catenin* / genetics
  • beta Catenin* / metabolism
  • p300-CBP Transcription Factors / genetics
  • p300-CBP Transcription Factors / metabolism

Substances

  • beta Catenin
  • Transcription Factors
  • Steroidogenic Factor 1
  • CTNNB1 protein, human
  • DNA-Binding Proteins
  • ARID1A protein, human
  • NR5A1 protein, human
  • Adaptor Proteins, Signal Transducing
  • YAP-Signaling Proteins
  • YAP1 protein, human
  • Forkhead Box Protein O3
  • Intrinsically Disordered Proteins
  • p300-CBP Transcription Factors
  • Nuclear Proteins
  • Phosphoproteins