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GIGYF2 and 4EHP Inhibit Translation Initiation of Defective Messenger RNAs to Assist Ribosome-Associated Quality Control.
- Source :
-
Molecular cell [Mol Cell] 2020 Sep 17; Vol. 79 (6), pp. 950-962.e6. Date of Electronic Publication: 2020 Jul 28. - Publication Year :
- 2020
-
Abstract
- Ribosome-associated quality control (RQC) pathways protect cells from toxicity caused by incomplete protein products resulting from translation of damaged or problematic mRNAs. Extensive work in yeast has identified highly conserved mechanisms that lead to degradation of faulty mRNA and partially synthesized polypeptides. Here we used CRISPR-Cas9-based screening to search for additional RQC strategies in mammals. We found that failed translation leads to specific inhibition of translation initiation on that message. This negative feedback loop is mediated by two translation inhibitors, GIGYF2 and 4EHP. Model substrates and growth-based assays established that inhibition of additional rounds of translation acts in concert with known RQC pathways to prevent buildup of toxic proteins. Inability to block translation of faulty mRNAs and subsequent accumulation of partially synthesized polypeptides could explain the neurodevelopmental and neuropsychiatric disorders observed in mice and humans with compromised GIGYF2 function.<br />Competing Interests: Declaration of Interests The authors declare no competing interests.<br /> (Published by Elsevier Inc.)
- Subjects :
- Animals
CRISPR-Cas Systems genetics
Humans
Mice
Protein Biosynthesis genetics
Protein Processing, Post-Translational genetics
Quality Control
RNA, Messenger genetics
Ubiquitin-Protein Ligases genetics
Carrier Proteins genetics
Eukaryotic Initiation Factor-4E genetics
Peptide Chain Initiation, Translational
Ribosomes genetics
Subjects
Details
- Language :
- English
- ISSN :
- 1097-4164
- Volume :
- 79
- Issue :
- 6
- Database :
- MEDLINE
- Journal :
- Molecular cell
- Publication Type :
- Academic Journal
- Accession number :
- 32726578
- Full Text :
- https://doi.org/10.1016/j.molcel.2020.07.007