Swi/Snf chromatin remodeling regulates transcriptional interference and gene repression

Mol Cell. 2024 Aug 22;84(16):3080-3097.e9. doi: 10.1016/j.molcel.2024.06.029. Epub 2024 Jul 22.

Abstract

Alternative transcription start sites can affect transcript isoform diversity and translation levels. In a recently described form of gene regulation, coordinated transcriptional and translational interference results in transcript isoform-dependent changes in protein expression. Specifically, a long undecoded transcript isoform (LUTI) is transcribed from a gene-distal promoter, interfering with expression of the gene-proximal promoter. Although transcriptional and chromatin features associated with LUTI expression have been described, the mechanism underlying LUTI-based transcriptional interference is not well understood. Using an unbiased genetic approach followed by functional genomics, we uncovered that the Swi/Snf chromatin remodeling complex is required for co-transcriptional nucleosome remodeling that leads to LUTI-based repression. We identified genes with tandem promoters that rely on Swi/Snf function for transcriptional interference during protein folding stress, including LUTI-regulated genes. This study provides clear evidence for Swi/Snf playing a direct role in gene repression via a cis transcriptional interference mechanism.

Keywords: LUTI; SWI/SNF; chromatin; chromatin remodeling; gene regulation; gene repression; transcription; transcription elongation; transcriptional interference; unfolded protein response.

MeSH terms

  • Chromatin / genetics
  • Chromatin / metabolism
  • Chromatin Assembly and Disassembly*
  • Chromosomal Proteins, Non-Histone* / genetics
  • Chromosomal Proteins, Non-Histone* / metabolism
  • Gene Expression Regulation, Fungal
  • Nucleosomes* / genetics
  • Nucleosomes* / metabolism
  • Promoter Regions, Genetic*
  • Saccharomyces cerevisiae Proteins* / genetics
  • Saccharomyces cerevisiae Proteins* / metabolism
  • Saccharomyces cerevisiae* / genetics
  • Saccharomyces cerevisiae* / metabolism
  • Transcription Factors* / genetics
  • Transcription Factors* / metabolism
  • Transcription Initiation Site
  • Transcription, Genetic*

Substances

  • Transcription Factors
  • Saccharomyces cerevisiae Proteins
  • Chromosomal Proteins, Non-Histone
  • Nucleosomes
  • SWI-SNF-B chromatin-remodeling complex
  • Chromatin