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Mechanisms by which in vitro meiotic arrest and sexual maturity improve developmental potential of mouse oocytes

To study the relationship between chromatin condensation, gene transcription and developmental competence during oocyte maturation and to explore the mechanisms by which meiotic arrest maintenance (MAM) and sexual maturity improve oocyte competence, we examined effects of MAM with roscovitine or db-...

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Autores principales: Chen, Fei, Lin, Juan, Sun, Xue, Xiao, Bin, Ning, Shu-Fen, Zhu, Shuai, Wang, Hui-Li, Tan, Jing-He
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5693946/
https://www.ncbi.nlm.nih.gov/pubmed/29150675
http://dx.doi.org/10.1038/s41598-017-16119-5
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author Chen, Fei
Lin, Juan
Sun, Xue
Xiao, Bin
Ning, Shu-Fen
Zhu, Shuai
Wang, Hui-Li
Tan, Jing-He
author_facet Chen, Fei
Lin, Juan
Sun, Xue
Xiao, Bin
Ning, Shu-Fen
Zhu, Shuai
Wang, Hui-Li
Tan, Jing-He
author_sort Chen, Fei
collection PubMed
description To study the relationship between chromatin condensation, gene transcription and developmental competence during oocyte maturation and to explore the mechanisms by which meiotic arrest maintenance (MAM) and sexual maturity improve oocyte competence, we examined effects of MAM with roscovitine or db-cAMP on chromatin condensation, gene transcription and developmental potential of NSN or SN oocytes from prepubertal or adult mice. MAM with roscovitine improved the developmental competence and global gene transcription of prepubertal NSN (prep-NSN) and adult-SN oocytes while having no effect on those of prep-SN oocytes. MAM with db-cAMP facilitated neither development nor transcription in any type of oocytes. MAM with either roscovitine or db-cAMP promoted chromatin condensation of prep-NSN oocytes. MAM with roscovitine promoted gene transcription and chromatin condensation simultaneously through inhibiting cyclin-dependent kinase (CDK) 5 and 2, respectively. The results suggested that MAM with roscovitine improved oocyte competence by promoting gene transcription via inhibiting CDK5. Oocyte cytoplasmic maturation is correlated with gene transcription but not with chromatin condensation. The difference in developmental competence between prepubertal NSN and SN oocytes and between prepubertal and adult SN oocytes was because while the former had not, the latter had completed or acquired the ability for transcription of important genes.
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spelling pubmed-56939462017-11-27 Mechanisms by which in vitro meiotic arrest and sexual maturity improve developmental potential of mouse oocytes Chen, Fei Lin, Juan Sun, Xue Xiao, Bin Ning, Shu-Fen Zhu, Shuai Wang, Hui-Li Tan, Jing-He Sci Rep Article To study the relationship between chromatin condensation, gene transcription and developmental competence during oocyte maturation and to explore the mechanisms by which meiotic arrest maintenance (MAM) and sexual maturity improve oocyte competence, we examined effects of MAM with roscovitine or db-cAMP on chromatin condensation, gene transcription and developmental potential of NSN or SN oocytes from prepubertal or adult mice. MAM with roscovitine improved the developmental competence and global gene transcription of prepubertal NSN (prep-NSN) and adult-SN oocytes while having no effect on those of prep-SN oocytes. MAM with db-cAMP facilitated neither development nor transcription in any type of oocytes. MAM with either roscovitine or db-cAMP promoted chromatin condensation of prep-NSN oocytes. MAM with roscovitine promoted gene transcription and chromatin condensation simultaneously through inhibiting cyclin-dependent kinase (CDK) 5 and 2, respectively. The results suggested that MAM with roscovitine improved oocyte competence by promoting gene transcription via inhibiting CDK5. Oocyte cytoplasmic maturation is correlated with gene transcription but not with chromatin condensation. The difference in developmental competence between prepubertal NSN and SN oocytes and between prepubertal and adult SN oocytes was because while the former had not, the latter had completed or acquired the ability for transcription of important genes. Nature Publishing Group UK 2017-11-17 /pmc/articles/PMC5693946/ /pubmed/29150675 http://dx.doi.org/10.1038/s41598-017-16119-5 Text en © The Author(s) 2017 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
Chen, Fei
Lin, Juan
Sun, Xue
Xiao, Bin
Ning, Shu-Fen
Zhu, Shuai
Wang, Hui-Li
Tan, Jing-He
Mechanisms by which in vitro meiotic arrest and sexual maturity improve developmental potential of mouse oocytes
title Mechanisms by which in vitro meiotic arrest and sexual maturity improve developmental potential of mouse oocytes
title_full Mechanisms by which in vitro meiotic arrest and sexual maturity improve developmental potential of mouse oocytes
title_fullStr Mechanisms by which in vitro meiotic arrest and sexual maturity improve developmental potential of mouse oocytes
title_full_unstemmed Mechanisms by which in vitro meiotic arrest and sexual maturity improve developmental potential of mouse oocytes
title_short Mechanisms by which in vitro meiotic arrest and sexual maturity improve developmental potential of mouse oocytes
title_sort mechanisms by which in vitro meiotic arrest and sexual maturity improve developmental potential of mouse oocytes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5693946/
https://www.ncbi.nlm.nih.gov/pubmed/29150675
http://dx.doi.org/10.1038/s41598-017-16119-5
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