K6-linked ubiquitylation marks formaldehyde-induced RNA-protein crosslinks for resolution.
Reactive aldehydes are produced by normal cellular metabolism or after alcohol consumption, and they accumulate in human tissues if aldehyde clearance mechanisms are impaired. Their toxicity has been attributed to the damage they cause to genomic DNA and the subsequent inhibition of transcription and replication. However, whether interference with other ... cellular processes contributes to aldehyde toxicity has not been investigated. We demonstrate that formaldehyde induces RNA-protein crosslinks (RPCs) that stall the ribosome and inhibit translation in human cells. RPCs in the messenger RNA (mRNA) are recognized by the translating ribosomes, marked by atypical K6-linked ubiquitylation catalyzed by the RING-in-between-RING (RBR) E3 ligase RNF14, and subsequently resolved by the ubiquitin- and ATP-dependent unfoldase VCP. Our findings uncover an evolutionary conserved formaldehyde-induced stress response pathway that protects cells against RPC accumulation in the cytoplasm, and they suggest that RPCs contribute to the cellular and tissue toxicity of reactive aldehydes.
Mesh Terms:
Aldehydes, Formaldehyde, Humans, RNA, RNA, Messenger, Ubiquitin-Protein Ligases, Ubiquitination
Aldehydes, Formaldehyde, Humans, RNA, RNA, Messenger, Ubiquitin-Protein Ligases, Ubiquitination
Mol Cell
Date: Dec. 07, 2023
PubMed ID: 37951215
View in: Pubmed Google Scholar
Download Curated Data For This Publication
259163
Switch View:
- Interactions 16