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EDF1 coordinates cellular responses to ribosome collisions.

Niladri K Sinha | Alban Ordureau | Katharina Best | James A Saba | Boris Zinshteyn | Elayanambi Sundaramoorthy | Amit Fulzele | Danielle M Garshott | Timo Denk | Matthias Thoms | Joao A Paulo | J Wade Harper | Eric J Bennett | Roland Beckmann | Rachel Green
eLife | 2020

Translation of aberrant mRNAs induces ribosomal collisions, thereby triggering pathways for mRNA and nascent peptide degradation and ribosomal rescue. Here we use sucrose gradient fractionation combined with quantitative proteomics to systematically identify proteins associated with collided ribosomes. This approach identified Endothelial differentiation-related factor 1 (EDF1) as a novel protein recruited to collided ribosomes during translational distress. Cryo-electron microscopic analyses of EDF1 and its yeast homolog Mbf1 revealed a conserved 40S ribosomal subunit binding site at the mRNA entry channel near the collision interface. EDF1 recruits the translational repressors GIGYF2 and EIF4E2 to collided ribosomes to initiate a negative-feedback loop that prevents new ribosomes from translating defective mRNAs. Further, EDF1 regulates an immediate-early transcriptional response to ribosomal collisions. Our results uncover mechanisms through which EDF1 coordinates multiple responses of the ribosome-mediated quality control pathway and provide novel insights into the intersection of ribosome-mediated quality control with global transcriptional regulation.

Pubmed ID: 32744497

Associated grants

  • Agency: NINDS NIH HHS, United States
    Id: R01 NS083524
  • Agency: NIGMS NIH HHS, United States
    Id: T32 GM136577
  • Agency: NIGMS NIH HHS, United States
    Id: R37 GM059425
  • Agency: National Science Foundation, International
    Id: DGE-1650112
  • Agency: Howard Hughes Medical Institute, United States
  • Agency: NIGMS NIH HHS, United States
    Id: R01 GM132129
  • Agency: NIGMS NIH HHS, United States
    Id: T32 GM007240
  • Agency: NIA NIH HHS, United States
    Id: AG011085
  • Agency: NIA NIH HHS, United States
    Id: R01 AG011085
  • Agency: NINDS NIH HHS, United States
    Id: R37 NS083524
  • Agency: NIGMS NIH HHS, United States
    Id: DP2 GM119132
  • Agency: NIGMS NIH HHS, United States
    Id: R01 GM136994
  • Agency: NIGMS NIH HHS, United States
    Id: 5K99GM135450-02
  • Agency: NIGMS NIH HHS, United States
    Id: K99 GM135450
  • Agency: Deutsche Forschungsgemeinschaft, International
    Id: GRK 1721

Publication data is provided by the National Library of Medicine ® and PubMed ®. Data is retrieved from PubMed ® on a weekly schedule. For terms and conditions see the National Library of Medicine Terms and Conditions.

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