Dedicated surveillance mechanism controls G-quadruplex forming non-coding RNAs in human mitochondria

Nat Commun. 2018 Jul 2;9(1):2558. doi: 10.1038/s41467-018-05007-9.

Abstract

The GC skew in vertebrate mitochondrial genomes results in synthesis of RNAs that are prone to form G-quadruplexes (G4s). Such RNAs, although mostly non-coding, are transcribed at high rates and are degraded by an unknown mechanism. Here we describe a dedicated mechanism of degradation of G4-containing RNAs, which is based on cooperation between mitochondrial degradosome and quasi-RNA recognition motif (qRRM) protein GRSF1. This cooperation prevents accumulation of G4-containing transcripts in human mitochondria. In vitro reconstitution experiments show that GRSF1 promotes G4 melting that facilitates degradosome-mediated decay. Among degradosome and GRSF1 regulated transcripts we identified one that undergoes post-transcriptional modification. We show that GRSF1 proteins form a distinct qRRM group found only in vertebrates. The appearance of GRSF1 coincided with changes in the mitochondrial genome, which allows the emergence of G4-containing RNAs. We propose that GRSF1 appearance is an evolutionary adaptation enabling control of G4 RNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • DEAD-box RNA Helicases / metabolism
  • Endoribonucleases / metabolism
  • Exoribonucleases / genetics
  • Exoribonucleases / metabolism
  • G-Quadruplexes*
  • Genome, Mitochondrial / genetics*
  • HEK293 Cells
  • HeLa Cells
  • Humans
  • Mitochondria / genetics
  • Mitochondria / metabolism*
  • Multienzyme Complexes / metabolism
  • Phylogeny
  • Poly(A)-Binding Proteins / genetics
  • Poly(A)-Binding Proteins / metabolism*
  • Polyribonucleotide Nucleotidyltransferase / metabolism
  • RNA Helicases / metabolism
  • RNA, Small Interfering / metabolism
  • RNA, Untranslated / genetics
  • RNA, Untranslated / metabolism*

Substances

  • GRSF1 protein, human
  • Multienzyme Complexes
  • Poly(A)-Binding Proteins
  • RNA, Small Interfering
  • RNA, Untranslated
  • degradosome
  • Polyribonucleotide Nucleotidyltransferase
  • Endoribonucleases
  • Exoribonucleases
  • PNPT1 protein, human
  • SUPV3L1 protein, human
  • DEAD-box RNA Helicases
  • RNA Helicases