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RNF219 regulates CCR4-NOT function in mRNA translation and deadenylation.

Aude GuénoléFabien VelillaAymeric ChartierApril RichAnne-Ruxandra CarvunisClaude SardetMartine SimoneligBijan Sobhian
Published in: Scientific reports (2022)
Post-transcriptional regulatory mechanisms play a role in many biological contexts through the control of mRNA degradation, translation and localization. Here, we show that the RING finger protein RNF219 co-purifies with the CCR4-NOT complex, the major mRNA deadenylase in eukaryotes, which mediates translational repression in both a deadenylase activity-dependent and -independent manner. Strikingly, RNF219 both inhibits the deadenylase activity of CCR4-NOT and enhances its capacity to repress translation of a target mRNA. We propose that the interaction of RNF219 with the CCR4-NOT complex directs the translational repressive activity of CCR4-NOT to a deadenylation-independent mechanism.
Keyphrases
  • dendritic cells
  • regulatory t cells
  • binding protein
  • dna damage response
  • transcription factor
  • immune response
  • oxidative stress
  • dna damage