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CNOT6 regulates a novel pattern of mRNA deadenylation during oocyte meiotic maturation
In many cell types, the length of the poly(A) tail of an mRNA is closely linked to its fate - a long tail is associated with active translation, a short tail with silencing and degradation. During mammalian oocyte development, two contrasting patterns of polyadenylation have been identified. Some mR...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5931610/ https://www.ncbi.nlm.nih.gov/pubmed/29717177 http://dx.doi.org/10.1038/s41598-018-25187-0 |
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author | Vieux, Karl-Frédéric Clarke, Hugh J. |
author_facet | Vieux, Karl-Frédéric Clarke, Hugh J. |
author_sort | Vieux, Karl-Frédéric |
collection | PubMed |
description | In many cell types, the length of the poly(A) tail of an mRNA is closely linked to its fate - a long tail is associated with active translation, a short tail with silencing and degradation. During mammalian oocyte development, two contrasting patterns of polyadenylation have been identified. Some mRNAs carry a long poly(A) tail during the growth stage and are actively translated, then become deadenylated and down-regulated during the subsequent stage, termed meiotic maturation. Other mRNAs carry a short tail poly(A) tail and are translationally repressed during growth, and their poly(A) tail lengthens and they become translationally activated during maturation. As well, a program of elimination of this ‘maternal’ mRNA is initiated during oocyte maturation. Here we describe a third pattern of polyadenylation: mRNAs are deadenylated in growing oocytes, become polyadenylated during early maturation and then deadenylated during late maturation. We show that the deadenylase, CNOT6, is present in cortical foci of oocytes and regulates deadenylation of these mRNAs, and that PUF-binding elements (PBEs) regulate deadenylation in mature oocytes. Unexpectedly, maintaining a long poly(A) tail neither enhances translation nor inhibits degradation of these mRNAs. Our findings implicate multiple machineries, more complex than previously thought, in regulating mRNA activity in oocytes. |
format | Online Article Text |
id | pubmed-5931610 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59316102018-08-29 CNOT6 regulates a novel pattern of mRNA deadenylation during oocyte meiotic maturation Vieux, Karl-Frédéric Clarke, Hugh J. Sci Rep Article In many cell types, the length of the poly(A) tail of an mRNA is closely linked to its fate - a long tail is associated with active translation, a short tail with silencing and degradation. During mammalian oocyte development, two contrasting patterns of polyadenylation have been identified. Some mRNAs carry a long poly(A) tail during the growth stage and are actively translated, then become deadenylated and down-regulated during the subsequent stage, termed meiotic maturation. Other mRNAs carry a short tail poly(A) tail and are translationally repressed during growth, and their poly(A) tail lengthens and they become translationally activated during maturation. As well, a program of elimination of this ‘maternal’ mRNA is initiated during oocyte maturation. Here we describe a third pattern of polyadenylation: mRNAs are deadenylated in growing oocytes, become polyadenylated during early maturation and then deadenylated during late maturation. We show that the deadenylase, CNOT6, is present in cortical foci of oocytes and regulates deadenylation of these mRNAs, and that PUF-binding elements (PBEs) regulate deadenylation in mature oocytes. Unexpectedly, maintaining a long poly(A) tail neither enhances translation nor inhibits degradation of these mRNAs. Our findings implicate multiple machineries, more complex than previously thought, in regulating mRNA activity in oocytes. Nature Publishing Group UK 2018-05-01 /pmc/articles/PMC5931610/ /pubmed/29717177 http://dx.doi.org/10.1038/s41598-018-25187-0 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Vieux, Karl-Frédéric Clarke, Hugh J. CNOT6 regulates a novel pattern of mRNA deadenylation during oocyte meiotic maturation |
title | CNOT6 regulates a novel pattern of mRNA deadenylation during oocyte meiotic maturation |
title_full | CNOT6 regulates a novel pattern of mRNA deadenylation during oocyte meiotic maturation |
title_fullStr | CNOT6 regulates a novel pattern of mRNA deadenylation during oocyte meiotic maturation |
title_full_unstemmed | CNOT6 regulates a novel pattern of mRNA deadenylation during oocyte meiotic maturation |
title_short | CNOT6 regulates a novel pattern of mRNA deadenylation during oocyte meiotic maturation |
title_sort | cnot6 regulates a novel pattern of mrna deadenylation during oocyte meiotic maturation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5931610/ https://www.ncbi.nlm.nih.gov/pubmed/29717177 http://dx.doi.org/10.1038/s41598-018-25187-0 |
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