Lost in Translation: Ribosome-Associated mRNA and Protein Quality Controls

Aberrant, misfolded, and mislocalized proteins are often toxic to cells and result in many human diseases. All proteins and their mRNA templates are subject to quality control. There are several distinct mechanisms that control the quality of mRNAs and proteins during translation at the ribosome. mR...

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Published inFrontiers in genetics Vol. 9; p. 431
Main Authors Karamyshev, Andrey L., Karamysheva, Zemfira N.
Format Journal Article
LanguageEnglish
Published Switzerland Frontiers Media S.A 04.10.2018
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ISSN1664-8021
1664-8021
DOI10.3389/fgene.2018.00431

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Summary:Aberrant, misfolded, and mislocalized proteins are often toxic to cells and result in many human diseases. All proteins and their mRNA templates are subject to quality control. There are several distinct mechanisms that control the quality of mRNAs and proteins during translation at the ribosome. mRNA quality control systems, nonsense-mediated decay, non-stop decay, and no-go decay detect premature stop codons, the absence of a natural stop codon, and stalled ribosomes in translation, respectively, and degrade their mRNAs. Defective truncated polypeptide nascent chains generated from faulty mRNAs are degraded by ribosome-associated protein quality control pathways. Regulation of aberrant protein production, a novel pathway, senses aberrant proteins by monitoring the status of nascent chain interactions during translation and triggers degradation of their mRNA. Here, we review the current progress in understanding of the molecular mechanisms of mRNA and protein quality controls at the ribosome during translation.
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Reviewed by: Tohru Yoshihisa, University of Hyogo, Japan; Woan-Yuh Tarn, Academia Sinica, Taiwan
Edited by: Maritza Jaramillo, National Institute of Scientific Research (INRS), Canada
This article was submitted to RNA, a section of the journal Frontiers in Genetics
ISSN:1664-8021
1664-8021
DOI:10.3389/fgene.2018.00431