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A position-specific 3′UTR sequence that accelerates mRNA decay
The 3′ untranslated regions (3′UTRs) of mammalian mRNAs direct an extensive range of alternative post-transcriptional outcomes, including regulation of mRNA decay and translation, contributing significantly to overall gene regulation. However, our knowledge of the underlying sequences and mechanisms...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5100352/ https://www.ncbi.nlm.nih.gov/pubmed/27565004 http://dx.doi.org/10.1080/15476286.2016.1225645 |
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author | Geissler, Rene Grimson, Andrew |
author_facet | Geissler, Rene Grimson, Andrew |
author_sort | Geissler, Rene |
collection | PubMed |
description | The 3′ untranslated regions (3′UTRs) of mammalian mRNAs direct an extensive range of alternative post-transcriptional outcomes, including regulation of mRNA decay and translation, contributing significantly to overall gene regulation. However, our knowledge of the underlying sequences and mechanisms is incomplete. We identified a novel 3′UTR sequence motif in mammals that targets mRNAs for transcript degradation. The motif is found in hundreds of mRNAs and is enriched in transcripts encoding regulatory proteins, such as transcription and signaling factors. Degradation of mRNAs containing the motif is mediated by the CCR4-NOT deadenylation complex. We identified hnRNPs A1 and A2/B1 as trans factors that directly bind to the motif, indicating a novel role for these proteins in deadenylation. Interestingly, a genome-wide analysis of the impact of this new regulatory pathway showed that the most active motifs are located within the 5′ and 3′-terminal portions of 3′UTRs, whereas elements in the center tend to be inactive. The highly position-specific function of the motif adds a new layer of regulation to gene expression mediated by 3′UTRs. |
format | Online Article Text |
id | pubmed-5100352 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-51003522016-11-23 A position-specific 3′UTR sequence that accelerates mRNA decay Geissler, Rene Grimson, Andrew RNA Biol Point of View The 3′ untranslated regions (3′UTRs) of mammalian mRNAs direct an extensive range of alternative post-transcriptional outcomes, including regulation of mRNA decay and translation, contributing significantly to overall gene regulation. However, our knowledge of the underlying sequences and mechanisms is incomplete. We identified a novel 3′UTR sequence motif in mammals that targets mRNAs for transcript degradation. The motif is found in hundreds of mRNAs and is enriched in transcripts encoding regulatory proteins, such as transcription and signaling factors. Degradation of mRNAs containing the motif is mediated by the CCR4-NOT deadenylation complex. We identified hnRNPs A1 and A2/B1 as trans factors that directly bind to the motif, indicating a novel role for these proteins in deadenylation. Interestingly, a genome-wide analysis of the impact of this new regulatory pathway showed that the most active motifs are located within the 5′ and 3′-terminal portions of 3′UTRs, whereas elements in the center tend to be inactive. The highly position-specific function of the motif adds a new layer of regulation to gene expression mediated by 3′UTRs. Taylor & Francis 2016-08-26 /pmc/articles/PMC5100352/ /pubmed/27565004 http://dx.doi.org/10.1080/15476286.2016.1225645 Text en © 2016 The Author(s). Published with license by Taylor & Francis Group, LLC 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. The moral rights of the named author(s) have been asserted. |
spellingShingle | Point of View Geissler, Rene Grimson, Andrew A position-specific 3′UTR sequence that accelerates mRNA decay |
title | A position-specific 3′UTR sequence that accelerates mRNA decay |
title_full | A position-specific 3′UTR sequence that accelerates mRNA decay |
title_fullStr | A position-specific 3′UTR sequence that accelerates mRNA decay |
title_full_unstemmed | A position-specific 3′UTR sequence that accelerates mRNA decay |
title_short | A position-specific 3′UTR sequence that accelerates mRNA decay |
title_sort | position-specific 3′utr sequence that accelerates mrna decay |
topic | Point of View |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5100352/ https://www.ncbi.nlm.nih.gov/pubmed/27565004 http://dx.doi.org/10.1080/15476286.2016.1225645 |
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