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Controlling the mitochondrial antisense - role of the SUV3-PNPase complex and its co-factor GRSF1 in mitochondrial RNA surveillance.

Zbigniew PietrasMagdalena A WojcikLukasz S BorowskiMaciej SzewczykTomasz M KulinskiDominik CysewskiPiotr P StepienAndrzej DziembowskiRoman J Szczesny
Published in: Molecular & cellular oncology (2018)
Transcription of the human mitochondrial genome produces a vast amount of non-coding antisense RNAs. These RNA species can form G-quadraplexes (G4), which affect their decay. We found that the mitochondrial degradosome, a complex of RNA helicase SUPV3L1 (best known as SUV3) and the ribonuclease PNPT1 (also known as PNPase), together with G4-melting protein GRSF1, is a key player in restricting antisense mtRNAs.
Keyphrases
  • oxidative stress
  • nucleic acid
  • public health
  • high resolution
  • transcription factor
  • gene expression
  • dna methylation
  • small molecule
  • protein protein
  • binding protein
  • amino acid
  • induced pluripotent stem cells