The ATPase BRG1/SMARCA4 is a protein interaction platform that recruits BAF subunits and the transcriptional repressor REST/NRSF in neural progenitor cells

Mol Cell Biochem. 2019 Nov;461(1-2):171-182. doi: 10.1007/s11010-019-03600-0. Epub 2019 Aug 20.

Abstract

The BAF complex (SWI/SNF) is an ATP-dependent chromatin remodeler that adapts the structural organization of the chromatin. Despite a growing understanding of the composition of BAF in different cell types, the interaction network within the BAF complex is poorly understood. Here, we characterized an isoform of the BRG1/SMARCA4 ATPase expressed in human neural progenitor cells. By electron microscopy and image processing, the neural BRG1/SMARCA4 shows an elongated globular structure, which provides a considerably larger surface than anticipated. We show that neural BRG1/SMARCA4 binds to BAF57/SMARCE1 and BAF60A/SMARCD1, two further components of BAF. Moreover, we demonstrate an interaction between the neural BRG1/SMARCA4 isoform and the central neurodevelopmental transcriptional repressor REST/NRSF. Our results provide insights into the assembly of a central transcriptional repressor complex, link the structure of the neural BRG1/SMARCA4 to its role as a protein-protein interaction platform and suggest BRG1/SMARCA4 as a key determinant that directs the BAF complex to specific DNA sites by interacting with transcription factors and regulators.

Keywords: BAF; BRG1/SMARCA4; Neural progenitor cells; Protein–protein interaction; REST/NRSF; SWI/SNF.

MeSH terms

  • Amino Acid Sequence
  • Cell Line
  • Chromosomal Proteins, Non-Histone / metabolism
  • DNA Helicases / chemistry
  • DNA Helicases / metabolism*
  • DNA-Binding Proteins / metabolism
  • Humans
  • Models, Biological
  • Neural Stem Cells / metabolism*
  • Nuclear Proteins / chemistry
  • Nuclear Proteins / metabolism*
  • Protein Binding
  • Protein Domains
  • Protein Isoforms / chemistry
  • Protein Isoforms / metabolism
  • Protein Subunits / metabolism*
  • Repressor Proteins / metabolism*
  • Transcription Factors / chemistry
  • Transcription Factors / metabolism*

Substances

  • Chromosomal Proteins, Non-Histone
  • DNA-Binding Proteins
  • Nuclear Proteins
  • Protein Isoforms
  • Protein Subunits
  • RE1-silencing transcription factor
  • Repressor Proteins
  • SMARCD1 protein, human
  • SMARCE1 protein, human
  • Transcription Factors
  • SMARCA4 protein, human
  • DNA Helicases