Pioneer-like factor GAF cooperates with PBAP (SWI/SNF) and NURF (ISWI) to regulate transcription

Genes Dev. 2021 Jan 1;35(1-2):147-156. doi: 10.1101/gad.341768.120. Epub 2020 Dec 10.

Abstract

Transcriptionally silent genes must be activated throughout development. This requires nucleosomes be removed from promoters and enhancers to allow transcription factor (TF) binding and recruitment of coactivators and RNA polymerase II (Pol II). Specialized pioneer TFs bind nucleosome-wrapped DNA to perform this chromatin opening by mechanisms that remain incompletely understood. Here, we show that GAGA factor (GAF), a Drosophila pioneer-like factor, functions with both SWI/SNF and ISWI family chromatin remodelers to allow recruitment of Pol II and entry to a promoter-proximal paused state, and also to promote Pol II's transition to productive elongation. We found that GAF interacts with PBAP (SWI/SNF) to open chromatin and allow Pol II to be recruited. Importantly, this activity is not dependent on NURF as previously proposed; however, GAF also synergizes with NURF downstream from this process to ensure efficient Pol II pause release and transition to productive elongation, apparently through its role in precisely positioning the +1 nucleosome. These results demonstrate how a single sequence-specific pioneer TF can synergize with remodelers to activate sets of genes. Furthermore, this behavior of remodelers is consistent with findings in yeast and mice, and likely represents general, conserved mechanisms found throughout eukarya.

Keywords: chromatin remodelers; pioneer factors; promoter-proximal pausing; transcription regulation.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adenosine Triphosphatases / metabolism*
  • Animals
  • Cell Line
  • Chromatin Assembly and Disassembly / genetics
  • DNA-Binding Proteins / metabolism*
  • Drosophila Proteins / metabolism*
  • Drosophila melanogaster / genetics*
  • Drosophila melanogaster / metabolism*
  • Gene Expression Regulation / genetics*
  • Protein Binding
  • RNA Polymerase II / metabolism
  • Ribonucleoprotein, U1 Small Nuclear / metabolism*
  • Transcription Elongation, Genetic
  • Transcription Factors / metabolism*

Substances

  • DNA-Binding Proteins
  • Drosophila Proteins
  • ISWI protein
  • Ribonucleoprotein, U1 Small Nuclear
  • SWI protein, D melanogaster
  • Transcription Factors
  • Trl protein, Drosophila
  • snf protein, Drosophila
  • RNA Polymerase II
  • Adenosine Triphosphatases