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Co-Translational Quality Control Induced by Translational Arrest

Genetic mutations, mRNA processing errors, and lack of availability of charged tRNAs sometimes slow down or completely stall translating ribosomes. Since an incomplete nascent chain derived from stalled ribosomes may function anomalously, such as by forming toxic aggregates, surveillance systems mon...

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Detalles Bibliográficos
Autores principales: Matsuo, Yoshitaka, Inada, Toshifumi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9953336/
https://www.ncbi.nlm.nih.gov/pubmed/36830686
http://dx.doi.org/10.3390/biom13020317
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author Matsuo, Yoshitaka
Inada, Toshifumi
author_facet Matsuo, Yoshitaka
Inada, Toshifumi
author_sort Matsuo, Yoshitaka
collection PubMed
description Genetic mutations, mRNA processing errors, and lack of availability of charged tRNAs sometimes slow down or completely stall translating ribosomes. Since an incomplete nascent chain derived from stalled ribosomes may function anomalously, such as by forming toxic aggregates, surveillance systems monitor every step of translation and dispose of such products to prevent their accumulation. Over the past decade, yeast models with powerful genetics and biochemical techniques have contributed to uncovering the mechanism of the co-translational quality control system, which eliminates the harmful products generated from aberrant translation. We here summarize the current knowledge of the molecular mechanism of the co-translational quality control systems in yeast, which eliminate the incomplete nascent chain, improper mRNAs, and faulty ribosomes to maintain cellular protein homeostasis.
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spelling pubmed-99533362023-02-25 Co-Translational Quality Control Induced by Translational Arrest Matsuo, Yoshitaka Inada, Toshifumi Biomolecules Review Genetic mutations, mRNA processing errors, and lack of availability of charged tRNAs sometimes slow down or completely stall translating ribosomes. Since an incomplete nascent chain derived from stalled ribosomes may function anomalously, such as by forming toxic aggregates, surveillance systems monitor every step of translation and dispose of such products to prevent their accumulation. Over the past decade, yeast models with powerful genetics and biochemical techniques have contributed to uncovering the mechanism of the co-translational quality control system, which eliminates the harmful products generated from aberrant translation. We here summarize the current knowledge of the molecular mechanism of the co-translational quality control systems in yeast, which eliminate the incomplete nascent chain, improper mRNAs, and faulty ribosomes to maintain cellular protein homeostasis. MDPI 2023-02-07 /pmc/articles/PMC9953336/ /pubmed/36830686 http://dx.doi.org/10.3390/biom13020317 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Matsuo, Yoshitaka
Inada, Toshifumi
Co-Translational Quality Control Induced by Translational Arrest
title Co-Translational Quality Control Induced by Translational Arrest
title_full Co-Translational Quality Control Induced by Translational Arrest
title_fullStr Co-Translational Quality Control Induced by Translational Arrest
title_full_unstemmed Co-Translational Quality Control Induced by Translational Arrest
title_short Co-Translational Quality Control Induced by Translational Arrest
title_sort co-translational quality control induced by translational arrest
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9953336/
https://www.ncbi.nlm.nih.gov/pubmed/36830686
http://dx.doi.org/10.3390/biom13020317
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