General Regulatory Factors Control the Fidelity of Transcription by Restricting Non-coding and Ectopic Initiation

Mol Cell. 2018 Dec 20;72(6):955-969.e7. doi: 10.1016/j.molcel.2018.11.037.

Abstract

The fidelity of transcription initiation is essential for accurate gene expression, but the determinants of start site selection are not fully understood. Rap1 and other general regulatory factors (GRFs) control the expression of many genes in yeast. We show that depletion of these factors induces widespread ectopic transcription initiation within promoters. This generates many novel non-coding RNAs and transcript isoforms with diverse stability, drastically altering the coding potential of the transcriptome. Ectopic transcription initiation strongly correlates with altered nucleosome positioning. We provide evidence that Rap1 can suppress ectopic initiation by a "place-holder" mechanism whereby it physically occludes inappropriate sites for pre-initiation complex formation. These results reveal an essential role for GRFs in the fidelity of transcription initiation and in the suppression of pervasive transcription, profoundly redefining current models for their function. They have important implications for the mechanism of transcription initiation and the control of gene expression.

Keywords: Abf1; Rap1; Reb1; chromatin remodelers; general regulatory factors; nucleosome depleted regions; nucleosome positioning; pervasive transcription; promoter directionality; transcription initiation fidelity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Binding Sites
  • Chromatin Assembly and Disassembly
  • Gene Expression Regulation, Fungal*
  • Nucleosomes / genetics
  • Nucleosomes / metabolism
  • Promoter Regions, Genetic
  • Protein Binding
  • RNA, Fungal / biosynthesis*
  • RNA, Fungal / genetics
  • RNA, Messenger / biosynthesis*
  • RNA, Messenger / genetics
  • RNA, Untranslated / genetics
  • RNA, Untranslated / metabolism*
  • Saccharomyces cerevisiae / genetics
  • Saccharomyces cerevisiae / metabolism*
  • Saccharomyces cerevisiae Proteins / genetics
  • Saccharomyces cerevisiae Proteins / metabolism*
  • Shelterin Complex
  • Telomere-Binding Proteins / genetics
  • Telomere-Binding Proteins / metabolism*
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Transcription Initiation Site
  • Transcription Initiation, Genetic
  • Transcription, Genetic*

Substances

  • Nucleosomes
  • RAP1 protein, S cerevisiae
  • RNA, Fungal
  • RNA, Messenger
  • RNA, Untranslated
  • Saccharomyces cerevisiae Proteins
  • Shelterin Complex
  • Telomere-Binding Proteins
  • Transcription Factors