The nascent polypeptide in the 60S subunit determines the Rqc2-dependency of ribosomal quality control

Nucleic Acids Res. 2021 Feb 26;49(4):2102-2113. doi: 10.1093/nar/gkab005.

Abstract

Ribosome stalling at tandem CGA codons or poly(A) sequences activates quality controls for nascent polypeptides including ribosome-associated quality control (RQC) and no-go mRNA decay (NGD). In RQC pathway, Hel2-dependent uS10 ubiquitination and the RQC-trigger (RQT) complex are essential for subunit dissociation, and Ltn1-dependent ubiquitination of peptidyl-tRNA in the 60S subunit requires Rqc2. Here, we report that polytryptophan sequences induce Rqc2-independent RQC. More than 11 consecutive tryptophan residues induced RQC in a manner dependent on Hel2-mediated ribosome ubiquitination and the RQT complex. Polytryptophan sequence-mediated RQC was not coupled with CAT-tailing, and Rqc2 was not required for Ltn1-dependent degradation of the arrest products. Eight consecutive tryptophan residues located at the region proximal to the peptidyl transferase center in the ribosome tunnel inhibited CAT-tailing by tandem CGA codons. Polytryptophan sequences also induced Hel2-mediated canonical RQC-coupled NGD and RQC-uncoupled NGD outside the stalled ribosomes. We propose that poly-tryptophan sequences induce Rqc2-independent RQC, suggesting that CAT-tailing in the 60S subunit could be modulated by the polypeptide in the ribosome exit tunnel.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Codon
  • Peptides / chemistry
  • Peptides / metabolism*
  • Protein Biosynthesis*
  • RNA Stability
  • RNA, Messenger / metabolism
  • RNA, Transfer, Amino Acyl / metabolism
  • RNA-Binding Proteins / physiology*
  • Ribosome Subunits, Large, Eukaryotic / metabolism*
  • Saccharomyces cerevisiae / genetics
  • Saccharomyces cerevisiae / metabolism
  • Saccharomyces cerevisiae Proteins / physiology*
  • Tryptophan / metabolism
  • Ubiquitination

Substances

  • Codon
  • Peptides
  • RNA, Messenger
  • RNA, Transfer, Amino Acyl
  • RNA-Binding Proteins
  • Saccharomyces cerevisiae Proteins
  • Tae2 protein, S cerevisiae
  • Tryptophan