Article ID Journal Published Year Pages File Type
2041631 Cell Reports 2012 7 Pages PDF
Abstract

SummaryBecause messenger RNAs without a stop codon (nonstop mRNAs) generate stalled ribosomes, cells have developed a mechanism allowing degradation of nonstop mRNAs and their translation products (nonstop proteins) in the cytosol. Here, we observe the fate of nonstop proteins destined for organelles such as the endoplasmic reticulum (ER) and mitochondria. Nonstop mRNAs for secretory-pathway proteins in yeast generate nonstop proteins that become stuck in the translocator, the Sec61 complex, in the ER membrane. These stuck nonstop secretory proteins avoid proteasomal degradation in the cytosol, but are instead released into the ER lumen through stalled ribosome and translocator channels by Dom34:Hbs1. We also found that nonstop mitochondrial proteins are cleared from the mitochondrial translocator, the TOM40 complex, by Dom34:Hbs1. Clearance of stuck nonstop proteins from organellar translocator channels is crucial for normal protein influx into organelles and for normal cell growth, especially when nonstop mRNA decay does not function efficiently.

Graphical AbstractFigure optionsDownload full-size imageDownload as PowerPoint slideHighlights► Nonstop secretory-pathway and mitochondrial proteins block translocators ► Dom34:Hbs1 clears organellar translocators of stuck nonstop proteins ► Such clearance and decay of nonstop proteins is essential

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