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mRNA quality control goes transcriptional

Eukaryotic mRNAs are extensively processed to generate functional transcripts, which are 5′ capped, spliced and 3′ polyadenylated. Accumulation of unprocessed (aberrant) mRNAs can be deleterious for the cell, hence processing fidelity is closely monitored by QC (quality control) mechanisms that iden...

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Detalles Bibliográficos
Autores principales: Kilchert, Cornelia, Vasiljeva, Lidia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3836415/
https://www.ncbi.nlm.nih.gov/pubmed/24256272
http://dx.doi.org/10.1042/BST20130202
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author Kilchert, Cornelia
Vasiljeva, Lidia
author_facet Kilchert, Cornelia
Vasiljeva, Lidia
author_sort Kilchert, Cornelia
collection PubMed
description Eukaryotic mRNAs are extensively processed to generate functional transcripts, which are 5′ capped, spliced and 3′ polyadenylated. Accumulation of unprocessed (aberrant) mRNAs can be deleterious for the cell, hence processing fidelity is closely monitored by QC (quality control) mechanisms that identify erroneous transcripts and initiate their selective removal. Nucleases including Xrn2/Rat1 and the nuclear exosome have been shown to play an important role in the turnover of aberrant mRNAs. Recently, with the growing appreciation that mRNA processing occurs concomitantly with polII (RNA polymerase II) transcription, it has become evident that QC acts at the transcriptional level in addition to degrading aberrant RNAs. In the present review, we discuss mechanisms that allow cells to co-transcriptionally initiate the removal of RNAs as well as down-regulate transcription of transcripts where processing repeatedly fails.
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spelling pubmed-38364152013-11-22 mRNA quality control goes transcriptional Kilchert, Cornelia Vasiljeva, Lidia Biochem Soc Trans Independent Meeting Eukaryotic mRNAs are extensively processed to generate functional transcripts, which are 5′ capped, spliced and 3′ polyadenylated. Accumulation of unprocessed (aberrant) mRNAs can be deleterious for the cell, hence processing fidelity is closely monitored by QC (quality control) mechanisms that identify erroneous transcripts and initiate their selective removal. Nucleases including Xrn2/Rat1 and the nuclear exosome have been shown to play an important role in the turnover of aberrant mRNAs. Recently, with the growing appreciation that mRNA processing occurs concomitantly with polII (RNA polymerase II) transcription, it has become evident that QC acts at the transcriptional level in addition to degrading aberrant RNAs. In the present review, we discuss mechanisms that allow cells to co-transcriptionally initiate the removal of RNAs as well as down-regulate transcription of transcripts where processing repeatedly fails. Portland Press Ltd. 2013-11-20 2013-12-01 /pmc/articles/PMC3836415/ /pubmed/24256272 http://dx.doi.org/10.1042/BST20130202 Text en © 2013 The author(s) has paid for this article to be freely available under the terms of the Creative Commons Attribution Licence (CC-BY)(http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Independent Meeting
Kilchert, Cornelia
Vasiljeva, Lidia
mRNA quality control goes transcriptional
title mRNA quality control goes transcriptional
title_full mRNA quality control goes transcriptional
title_fullStr mRNA quality control goes transcriptional
title_full_unstemmed mRNA quality control goes transcriptional
title_short mRNA quality control goes transcriptional
title_sort mrna quality control goes transcriptional
topic Independent Meeting
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3836415/
https://www.ncbi.nlm.nih.gov/pubmed/24256272
http://dx.doi.org/10.1042/BST20130202
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