Quality control of transcription start site selection by nonsense-mediated-mRNA decay

Elife. 2015 Apr 23:4:e06722. doi: 10.7554/eLife.06722.

Abstract

Nonsense-mediated mRNA decay (NMD) is a translation-dependent RNA quality-control pathway targeting transcripts such as messenger RNAs harboring premature stop-codons or short upstream open reading frame (uORFs). Our transcription start sites (TSSs) analysis of Saccharomyces cerevisiae cells deficient for RNA degradation pathways revealed that about half of the pervasive transcripts are degraded by NMD, which provides a fail-safe mechanism to remove spurious transcripts that escaped degradation in the nucleus. Moreover, we found that the low specificity of RNA polymerase II TSSs selection generates, for 47% of the expressed genes, NMD-sensitive transcript isoforms carrying uORFs or starting downstream of the ATG START codon. Despite the low abundance of this last category of isoforms, their presence seems to constrain genomic sequences, as suggested by the significant bias against in-frame ATGs specifically found at the beginning of the corresponding genes and reflected by a depletion of methionines in the N-terminus of the encoded proteins.

Keywords: RNA quality control; S. cerevisiae; chromosomes; evolutionary biology; genes; genomics; non-coding RNAs; non-sense mediated mRNA decay; nuclear RNA degradation; transcription initiation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Codon, Nonsense
  • Gene Expression Regulation, Fungal
  • Nonsense Mediated mRNA Decay*
  • Open Reading Frames
  • RNA Polymerase II / genetics
  • RNA Polymerase II / metabolism
  • RNA, Fungal / genetics*
  • RNA, Fungal / metabolism
  • RNA, Messenger / genetics*
  • RNA, Messenger / metabolism
  • Saccharomyces cerevisiae / genetics*
  • Saccharomyces cerevisiae / metabolism
  • Saccharomyces cerevisiae Proteins / genetics*
  • Saccharomyces cerevisiae Proteins / metabolism
  • Transcription Initiation Site

Substances

  • Codon, Nonsense
  • RNA, Fungal
  • RNA, Messenger
  • Saccharomyces cerevisiae Proteins
  • RNA Polymerase II

Associated data

  • GEO/GSE64139

Grants and funding

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.