Article

Dom34:Hbs1 Plays a General Role in Quality-Control Systems by Dissociation of a Stalled Ribosome at the 3′ End of Aberrant mRNA

Graduate School of Pharmaceutical Science, Tohoku University, Sendai, Japan.
Molecular cell (Impact Factor: 14.02). 04/2012; 46(4):518-29. DOI: 10.1016/j.molcel.2012.03.013
Source: PubMed

ABSTRACT

Translation arrest leads to an endonucleolytic cleavage of mRNA that is termed no-go decay (NGD). It has been reported that the Dom34:Hbs1 complex stimulates this endonucleolytic cleavage of mRNA induced by translation arrest in vivo and dissociates subunits of a stalled ribosome in vitro. Here we report that Dom34:Hbs1 dissociates the subunits of a ribosome that is stalled at the 3' end of mRNA in vivo, and has a crucial role in both NGD and nonstop decay. Dom34:Hbs1-mediated dissociation of a ribosome that is stalled at the 3' end of mRNA is required for degradation of a 5'-NGD intermediate. Dom34:Hbs1 facilitates the decay of nonstop mRNAs from the 3' end by exosomes and is required for the complete degradation of nonstop mRNA decay intermediates. We propose that Dom34:Hbs1 stimulates degradation of the 5'-NGD intermediate and of nonstop mRNA by dissociating the ribosome that is stalled at the 3' end of the mRNA.

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Available from: Toshifumi Inada, Apr 01, 2014
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    • "In a recent report, Wu et al. (2014) demonstrated that Pelo is required for enhanced structural protein synthesis during dicistrovirus infection but does not affect IGR IRES translation[57]. Pelo is the Drosophila homolog for Dom34, which is responsible for the recycling of stalled 80S ribosomes on mRNAs[58].Wu et al. (2014)speculated that the action of Pelo during infection provides dicistrovirus genomes greater access to ribosomes for high level synthesis of viral structural proteins[58]. Nevertheless, in cells depleted of Pelo, dicistrovirus structural proteins are still expressed in supramolar excess over non-structural proteins[57], thus ribosome recycling is likely not the sole reason for structural protein synthesis that is observed late in infection. "

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    • "These observations strongly suggest oxidized mRNA is a primary target of ribosome-based mRNA quality-control processes. We note that NGD and in particular Dom34 has been implicated in a number of processes; for example, Inada and colleagues have shown the factor to be important in rescuing ribosomes trapped on truncated mRNA (Tsuboi et al., 2012). Recently, Guydosh and Green used ribosomal profiling to show that in the absence of the factor, ribosomes venture into the 3 0 UTR (Guydosh and Green, 2014). "
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    ABSTRACT: Chemical damage to RNA affects its functional properties and thus may pose a significant hurdle to the translational apparatus; however, the effects of damaged mRNA on the speed and accuracy of the decoding process and their interplay with quality-control processes are not known. Here, we systematically explore the effects of oxidative damage on the decoding process using a well-defined bacterial in vitro translation system. We find that the oxidative lesion 8-oxoguanosine (8-oxoG) reduces the rate of peptide-bond formation by more than three orders of magnitude independent of its position within the codon. Interestingly, 8-oxoG had little effect on the fidelity of the selection process, suggesting that the modification stalls the translational machinery. Consistent with these findings, 8-oxoG mRNAs were observed to accumulate and associate with polyribosomes in yeast strains in which no-go decay is compromised. Our data provide compelling evidence that mRNA-surveillance mechanisms have evolved to cope with damaged mRNA. Copyright © 2014 The Authors. Published by Elsevier Inc. All rights reserved.
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    • "Nonsense-mediated mRNA decay (NMD) is one of three conserved eukaryotic surveillance pathways ensuring mRNA quality control in the cytoplasm [1] [2] [3] [4]. NMD is activated by mechanistic differences between normal and premature translation termination and utilizes three conserved factors (Upf1, Upf2, and Upf3) [5] [6] [7] to couple nonsense codon recognition to the release factors (eRF1 and eRF3), the ribosome, and the mRNA decapping complex [8] [9] [10] [11] [12] [13] [14]. "
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