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Cleavage and polyadenylation: Ending the message expands gene regulation

Cleavage and polyadenylation (pA) is a fundamental step that is required for the maturation of primary protein encoding transcripts into functional mRNAs that can be exported from the nucleus and translated in the cytoplasm. 3′end processing is dependent on the assembly of a multiprotein processing...

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Autores principales: Neve, Jonathan, Patel, Radhika, Wang, Zhiqiao, Louey, Alastair, Furger, André Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5546720/
https://www.ncbi.nlm.nih.gov/pubmed/28453393
http://dx.doi.org/10.1080/15476286.2017.1306171
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author Neve, Jonathan
Patel, Radhika
Wang, Zhiqiao
Louey, Alastair
Furger, André Martin
author_facet Neve, Jonathan
Patel, Radhika
Wang, Zhiqiao
Louey, Alastair
Furger, André Martin
author_sort Neve, Jonathan
collection PubMed
description Cleavage and polyadenylation (pA) is a fundamental step that is required for the maturation of primary protein encoding transcripts into functional mRNAs that can be exported from the nucleus and translated in the cytoplasm. 3′end processing is dependent on the assembly of a multiprotein processing complex on the pA signals that reside in the pre-mRNAs. Most eukaryotic genes have multiple pA signals, resulting in alternative cleavage and polyadenylation (APA), a widespread phenomenon that is important to establish cell state and cell type specific transcriptomes. Here, we review how pA sites are recognized and comprehensively summarize how APA is regulated and creates mRNA isoform profiles that are characteristic for cell types, tissues, cellular states and disease.
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spelling pubmed-55467202017-08-15 Cleavage and polyadenylation: Ending the message expands gene regulation Neve, Jonathan Patel, Radhika Wang, Zhiqiao Louey, Alastair Furger, André Martin RNA Biol Review Cleavage and polyadenylation (pA) is a fundamental step that is required for the maturation of primary protein encoding transcripts into functional mRNAs that can be exported from the nucleus and translated in the cytoplasm. 3′end processing is dependent on the assembly of a multiprotein processing complex on the pA signals that reside in the pre-mRNAs. Most eukaryotic genes have multiple pA signals, resulting in alternative cleavage and polyadenylation (APA), a widespread phenomenon that is important to establish cell state and cell type specific transcriptomes. Here, we review how pA sites are recognized and comprehensively summarize how APA is regulated and creates mRNA isoform profiles that are characteristic for cell types, tissues, cellular states and disease. Taylor & Francis 2017-04-28 /pmc/articles/PMC5546720/ /pubmed/28453393 http://dx.doi.org/10.1080/15476286.2017.1306171 Text en © 2017 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted 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 Review
Neve, Jonathan
Patel, Radhika
Wang, Zhiqiao
Louey, Alastair
Furger, André Martin
Cleavage and polyadenylation: Ending the message expands gene regulation
title Cleavage and polyadenylation: Ending the message expands gene regulation
title_full Cleavage and polyadenylation: Ending the message expands gene regulation
title_fullStr Cleavage and polyadenylation: Ending the message expands gene regulation
title_full_unstemmed Cleavage and polyadenylation: Ending the message expands gene regulation
title_short Cleavage and polyadenylation: Ending the message expands gene regulation
title_sort cleavage and polyadenylation: ending the message expands gene regulation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5546720/
https://www.ncbi.nlm.nih.gov/pubmed/28453393
http://dx.doi.org/10.1080/15476286.2017.1306171
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