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When a ribosome encounters a premature termination codon

In mammalian cells, aberrant transcripts harboring a premature termination codon (PTC) can be generated by abnormal or inefficient biogenesis of mRNAs or by somatic mutation. Truncated polypeptides synthesized from these aberrant transcripts could be toxic to normal cellular functions. However, mamm...

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Detalles Bibliográficos
Autores principales: Hwang, Jungwook, Kim, Yoon Ki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Biochemistry and Molecular Biology 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4133823/
https://www.ncbi.nlm.nih.gov/pubmed/23351378
http://dx.doi.org/10.5483/BMBRep.2013.46.1.002
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author Hwang, Jungwook
Kim, Yoon Ki
author_facet Hwang, Jungwook
Kim, Yoon Ki
author_sort Hwang, Jungwook
collection PubMed
description In mammalian cells, aberrant transcripts harboring a premature termination codon (PTC) can be generated by abnormal or inefficient biogenesis of mRNAs or by somatic mutation. Truncated polypeptides synthesized from these aberrant transcripts could be toxic to normal cellular functions. However, mammalian cells have evolved sophisticated mechanisms for monitoring the quality of mRNAs. The faulty transcripts harboring PTC are subject to nonsense-mediated mRNA decay (NMD), nonsense-mediated translational repression (NMTR), nonsense-associated alternative splicing (NAS), or nonsense-mediated transcriptional gene silencing (NMTGS). In this review, we briefly outline the molecular characteristics of each pathway and suggest mRNA quality control mechanisms as a means to regulate normal gene expression. [BMB Reports 2013; 46(1): 9-16]
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spelling pubmed-41338232014-09-16 When a ribosome encounters a premature termination codon Hwang, Jungwook Kim, Yoon Ki BMB Rep Review Article In mammalian cells, aberrant transcripts harboring a premature termination codon (PTC) can be generated by abnormal or inefficient biogenesis of mRNAs or by somatic mutation. Truncated polypeptides synthesized from these aberrant transcripts could be toxic to normal cellular functions. However, mammalian cells have evolved sophisticated mechanisms for monitoring the quality of mRNAs. The faulty transcripts harboring PTC are subject to nonsense-mediated mRNA decay (NMD), nonsense-mediated translational repression (NMTR), nonsense-associated alternative splicing (NAS), or nonsense-mediated transcriptional gene silencing (NMTGS). In this review, we briefly outline the molecular characteristics of each pathway and suggest mRNA quality control mechanisms as a means to regulate normal gene expression. [BMB Reports 2013; 46(1): 9-16] Korean Society for Biochemistry and Molecular Biology 2013-01 /pmc/articles/PMC4133823/ /pubmed/23351378 http://dx.doi.org/10.5483/BMBRep.2013.46.1.002 Text en Copyright © 2013, Korean Society for Biochemistry and Molecular Biology http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Hwang, Jungwook
Kim, Yoon Ki
When a ribosome encounters a premature termination codon
title When a ribosome encounters a premature termination codon
title_full When a ribosome encounters a premature termination codon
title_fullStr When a ribosome encounters a premature termination codon
title_full_unstemmed When a ribosome encounters a premature termination codon
title_short When a ribosome encounters a premature termination codon
title_sort when a ribosome encounters a premature termination codon
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4133823/
https://www.ncbi.nlm.nih.gov/pubmed/23351378
http://dx.doi.org/10.5483/BMBRep.2013.46.1.002
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