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A role of Pumilio 1 in mammalian oocyte maturation and maternal phase of embryogenesis

BACKGROUND: RNA binding proteins play a pivotal role during the oocyte-to-embryo transition and maternal phase of embryogenesis in invertebrates, but their function in these processes in mammalian systems remain largely understudied. RESULTS: Here we report that a member of the Pumilio/FBF family of...

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Autores principales: Mak, Winifred, Xia, Jing, Cheng, Ee-Chun, Lowther, Katie, Lin, Haifan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6194604/
https://www.ncbi.nlm.nih.gov/pubmed/30364263
http://dx.doi.org/10.1186/s13578-018-0251-1
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author Mak, Winifred
Xia, Jing
Cheng, Ee-Chun
Lowther, Katie
Lin, Haifan
author_facet Mak, Winifred
Xia, Jing
Cheng, Ee-Chun
Lowther, Katie
Lin, Haifan
author_sort Mak, Winifred
collection PubMed
description BACKGROUND: RNA binding proteins play a pivotal role during the oocyte-to-embryo transition and maternal phase of embryogenesis in invertebrates, but their function in these processes in mammalian systems remain largely understudied. RESULTS: Here we report that a member of the Pumilio/FBF family of RNA binding proteins in mice, Pumilio 1 (Pum1), is a maternal effect gene. The absence of maternal PUM1 in the oocyte does not affect meiotic maturation but leads to abnormal preimplantation development. Furthermore, genome-wide transcriptome analysis of oocytes and embryos revealed that there is a concomitant perturbation of the mRNA milieu. Of note, putative PUM1 mRNA targets were equally perturbed as non-direct targets, which indicates that PUM1 regulates the stability of maternal mRNAs both directly and indirectly. We show Cdk1 mRNA, a known PUM1 target essential for meiosis and preimplantation development, is not degraded appropriately during meiosis, leading to an increase in CDK1 protein in mature oocytes, which indicates that PUM1 post-transcriptionally regulates Cdk1 mRNA; this could partially explain the observed abnormal preimplantation development. Furthermore, our results show that maternal and zygotic PUM1 are required for postnatal survival. CONCLUSIONS: These findings indicate that PUM1 is essential in the process of cytoplasmic maturation and developmental competence of the oocyte. These results reveal an important function of maternal PUM1 as a post-transcriptional regulator during mammalian embryogenesis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13578-018-0251-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-61946042018-10-25 A role of Pumilio 1 in mammalian oocyte maturation and maternal phase of embryogenesis Mak, Winifred Xia, Jing Cheng, Ee-Chun Lowther, Katie Lin, Haifan Cell Biosci Research BACKGROUND: RNA binding proteins play a pivotal role during the oocyte-to-embryo transition and maternal phase of embryogenesis in invertebrates, but their function in these processes in mammalian systems remain largely understudied. RESULTS: Here we report that a member of the Pumilio/FBF family of RNA binding proteins in mice, Pumilio 1 (Pum1), is a maternal effect gene. The absence of maternal PUM1 in the oocyte does not affect meiotic maturation but leads to abnormal preimplantation development. Furthermore, genome-wide transcriptome analysis of oocytes and embryos revealed that there is a concomitant perturbation of the mRNA milieu. Of note, putative PUM1 mRNA targets were equally perturbed as non-direct targets, which indicates that PUM1 regulates the stability of maternal mRNAs both directly and indirectly. We show Cdk1 mRNA, a known PUM1 target essential for meiosis and preimplantation development, is not degraded appropriately during meiosis, leading to an increase in CDK1 protein in mature oocytes, which indicates that PUM1 post-transcriptionally regulates Cdk1 mRNA; this could partially explain the observed abnormal preimplantation development. Furthermore, our results show that maternal and zygotic PUM1 are required for postnatal survival. CONCLUSIONS: These findings indicate that PUM1 is essential in the process of cytoplasmic maturation and developmental competence of the oocyte. These results reveal an important function of maternal PUM1 as a post-transcriptional regulator during mammalian embryogenesis. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13578-018-0251-1) contains supplementary material, which is available to authorized users. BioMed Central 2018-10-19 /pmc/articles/PMC6194604/ /pubmed/30364263 http://dx.doi.org/10.1186/s13578-018-0251-1 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Mak, Winifred
Xia, Jing
Cheng, Ee-Chun
Lowther, Katie
Lin, Haifan
A role of Pumilio 1 in mammalian oocyte maturation and maternal phase of embryogenesis
title A role of Pumilio 1 in mammalian oocyte maturation and maternal phase of embryogenesis
title_full A role of Pumilio 1 in mammalian oocyte maturation and maternal phase of embryogenesis
title_fullStr A role of Pumilio 1 in mammalian oocyte maturation and maternal phase of embryogenesis
title_full_unstemmed A role of Pumilio 1 in mammalian oocyte maturation and maternal phase of embryogenesis
title_short A role of Pumilio 1 in mammalian oocyte maturation and maternal phase of embryogenesis
title_sort role of pumilio 1 in mammalian oocyte maturation and maternal phase of embryogenesis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6194604/
https://www.ncbi.nlm.nih.gov/pubmed/30364263
http://dx.doi.org/10.1186/s13578-018-0251-1
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