Introns Protect Eukaryotic Genomes from Transcription-Associated Genetic Instability

Mol Cell. 2017 Aug 17;67(4):608-621.e6. doi: 10.1016/j.molcel.2017.07.002. Epub 2017 Jul 27.

Abstract

Transcription is a source of genetic instability that can notably result from the formation of genotoxic DNA:RNA hybrids, or R-loops, between the nascent mRNA and its template. Here we report an unexpected function for introns in counteracting R-loop accumulation in eukaryotic genomes. Deletion of endogenous introns increases R-loop formation, while insertion of an intron into an intronless gene suppresses R-loop accumulation and its deleterious impact on transcription and recombination in yeast. Recruitment of the spliceosome onto the mRNA, but not splicing per se, is shown to be critical to attenuate R-loop formation and transcription-associated genetic instability. Genome-wide analyses in a number of distant species differing in their intron content, including human, further revealed that intron-containing genes and the intron-richest genomes are best protected against R-loop accumulation and subsequent genetic instability. Our results thereby provide a possible rationale for the conservation of introns throughout the eukaryotic lineage.

Keywords: R-loops; genetic instability; intron; mRNA splicing; mRNP; messenger ribonucleoparticle; recombination; transcription.

MeSH terms

  • Candida glabrata / genetics
  • Candida glabrata / metabolism
  • Cell Line
  • Computational Biology
  • Cryptococcus neoformans / genetics
  • Cryptococcus neoformans / metabolism
  • DNA Damage
  • DNA, Fungal / chemistry
  • DNA, Fungal / genetics*
  • DNA, Fungal / metabolism
  • Databases, Genetic
  • Fungal Proteins / genetics
  • Fungal Proteins / metabolism
  • Gene Expression Regulation, Fungal
  • Genomic Instability*
  • Genotype
  • Humans
  • Introns*
  • Nucleic Acid Conformation
  • Nucleic Acid Heteroduplexes / chemistry
  • Nucleic Acid Heteroduplexes / genetics*
  • Nucleic Acid Heteroduplexes / metabolism
  • Phenotype
  • RNA Splicing
  • RNA, Fungal / chemistry
  • RNA, Fungal / genetics*
  • RNA, Fungal / metabolism
  • Ribonucleoproteins / genetics
  • Ribonucleoproteins / metabolism
  • Saccharomyces cerevisiae / genetics
  • Saccharomyces cerevisiae / metabolism
  • Schizosaccharomyces / genetics
  • Schizosaccharomyces / metabolism
  • Spliceosomes / genetics
  • Spliceosomes / metabolism
  • Structure-Activity Relationship
  • Transcription, Genetic*

Substances

  • DNA, Fungal
  • Fungal Proteins
  • Nucleic Acid Heteroduplexes
  • RNA, Fungal
  • Ribonucleoproteins
  • messenger ribonucleoprotein