Integrated genomic analysis reveals key features of long undecoded transcript isoform-based gene repression

Mol Cell. 2021 May 20;81(10):2231-2245.e11. doi: 10.1016/j.molcel.2021.03.013. Epub 2021 Apr 6.

Abstract

Long undecoded transcript isoforms (LUTIs) represent a class of non-canonical mRNAs that downregulate gene expression through the combined act of transcriptional and translational repression. While single gene studies revealed important aspects of LUTI-based repression, how these features affect gene regulation on a global scale is unknown. Using transcript leader and direct RNA sequencing, here, we identify 74 LUTI candidates that are specifically induced in meiotic prophase. Translational repression of these candidates appears to be ubiquitous and is dependent on upstream open reading frames. However, LUTI-based transcriptional repression is variable. In only 50% of the cases, LUTI transcription causes downregulation of the protein-coding transcript isoform. Higher LUTI expression, enrichment of histone 3 lysine 36 trimethylation, and changes in nucleosome position are the strongest predictors of LUTI-based transcriptional repression. We conclude that LUTIs downregulate gene expression in a manner that integrates translational repression, chromatin state changes, and the magnitude of LUTI expression.

Keywords: H3K36; LUTI; chromatin; differentiation; gene expression; isoform; meiosis; transcription factor; translation; uORF.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromatin / metabolism
  • Gene Expression Regulation, Fungal*
  • Genes, Reporter
  • Genomics*
  • Meiosis / genetics
  • Nanopore Sequencing
  • Nucleosomes / metabolism
  • Open Reading Frames / genetics
  • Promoter Regions, Genetic / genetics
  • Prophase / genetics
  • Protein Biosynthesis / genetics
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Saccharomyces cerevisiae / genetics*
  • Transcription Factors / metabolism
  • Transcription, Genetic

Substances

  • Chromatin
  • Nucleosomes
  • Protein Isoforms
  • RNA, Messenger
  • Transcription Factors