The E3 ubiquitin ligase RNF10 modifies 40S ribosomal subunits of ribosomes compromised in translation

• DOI: 10.1016/j.celrep.2021.109468
• Publication Date: 2021-08-03T16:16:33Z
• Authors: Aitor Garzia; Cindy Meyer; Thomas Tuschl
• Keywords: Ribosomal Proteins; Ribosome Subunits, Small, Eukaryotic; 0301 basic medicine; Ubiquitination; Models, Biological; 03 medical and health sciences; Cross-Linking Reagents; HEK293 Cells; Protein Domains; RNA, Transfer; Protein Biosynthesis; Mutation; Humans; RNA, Messenger; Carrier Proteins; Peptides; Ubiquitin Thiolesterase

Reversible monoubiquitination of small subunit ribosomal proteins RPS2/uS5 and RPS3/uS3 has been noted to occur on ribosomes involved in ZNF598-dependent mRNA surveillance. Subsequent deubiquitination of RPS2 and RPS3 by USP10 is critical for recycling of stalled ribosomes in a process known as ribosome-associated quality control. Here, we identify and characterize the RPS2- and RPS3-specific E3 ligase Really Interesting New Gene (RING) finger protein 10 (RNF10) and its role in translation. Overexpression of RNF10 increases 40S ribosomal subunit degradation similarly to the knockout of USP10. Although a substantial fraction of RNF10-mediated RPS2 and RPS3 monoubiquitination results from ZNF598-dependent sensing of collided ribosomes, ZNF598-independent impairment of translation initiation and elongation also contributes to RPS2 and RPS3 monoubiquitination. RNF10 photoactivatable ribonucleoside-enhanced crosslinking and immunoprecipitation (PAR-CLIP) identifies crosslinked mRNAs, tRNAs, and 18S rRNAs, indicating recruitment of RNF10 to ribosomes stalled in translation. These impeded ribosomes are tagged by ubiquitin at their 40S subunit for subsequent programmed degradation unless rescued by USP10.