Structure and function of Vms1 and Arb1 in RQC and mitochondrial proteome homeostasis

Ting Su, Toshiaki Izawa, Matthias Thoms, Yui Yamashita, Jingdong Cheng, Otto Berninghausen, F. Ulrich Hartl, Toshifumi Inada, Walter Neupert, Roland Beckmann

Research output: Contribution to journalArticlepeer-review

10 Citations (Scopus)

Abstract

Ribosome-associated quality control (RQC) provides a rescue pathway for eukaryotic cells to process faulty proteins after translational stalling of cytoplasmic ribosomes1–6. After dissociation of ribosomes, the stalled tRNA-bound peptide remains associated with the 60S subunit and extended by Rqc2 by addition of C-terminal alanyl and threonyl residues (CAT tails)7–9, whereas Vms1 catalyses cleavage and release of the peptidyl-tRNA before or after addition of CAT tails10–12. In doing so, Vms1 counteracts CAT-tailing of nuclear-encoded mitochondrial proteins that otherwise drive aggregation and compromise mitochondrial and cellular homeostasis13. Here we present structural and functional insights into the interaction of Saccharomyces cerevisiae Vms1 with 60S subunits in pre- and post-peptidyl-tRNA cleavage states. Vms1 binds to 60S subunits with its Vms1-like release factor 1 (VLRF1), zinc finger and ankyrin domains. VLRF1 overlaps with the Rqc2 A-tRNA position and interacts with the ribosomal A-site, projecting its catalytic GSQ motif towards the CCA end of the tRNA, its Y285 residue dislodging the tRNA A73 for nucleolytic cleavage. Moreover, in the pre-state, we found the ABCF-type ATPase Arb1 in the ribosomal E-site, which stabilizes the delocalized A73 of the peptidyl-tRNA and stimulates Vms1-dependent tRNA cleavage. Our structural analysis provides mechanistic insights into the interplay of the RQC factors Vms1, Rqc2 and Arb1 and their role in the protection of mitochondria from the aggregation of toxic proteins.

Original languageEnglish
Pages (from-to)538-542
Number of pages5
JournalNature
Volume570
Issue number7762
DOIs
Publication statusPublished - 2019 Jun 27

ASJC Scopus subject areas

  • General

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