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Casein kinase 2 modulates the spindle assembly checkpoint to orchestrate porcine oocyte meiotic progression

BACKGROUND: CK2 (casein kinase 2) is a serine/threonine-selective protein kinase that has been involved in a variety of cellular processes such as DNA repair, cell cycle control and circadian rhythm regulation. However, its functional roles in oocyte meiosis have not been fully determined. RESULTS:...

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Autores principales: ShiYang, Xiayan, Miao, Yilong, Cui, Zhaokang, Lu, Yajuan, Zhou, Changyin, Zhang, Yu, Xiong, Bo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7140493/
https://www.ncbi.nlm.nih.gov/pubmed/32292585
http://dx.doi.org/10.1186/s40104-020-00438-1
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author ShiYang, Xiayan
Miao, Yilong
Cui, Zhaokang
Lu, Yajuan
Zhou, Changyin
Zhang, Yu
Xiong, Bo
author_facet ShiYang, Xiayan
Miao, Yilong
Cui, Zhaokang
Lu, Yajuan
Zhou, Changyin
Zhang, Yu
Xiong, Bo
author_sort ShiYang, Xiayan
collection PubMed
description BACKGROUND: CK2 (casein kinase 2) is a serine/threonine-selective protein kinase that has been involved in a variety of cellular processes such as DNA repair, cell cycle control and circadian rhythm regulation. However, its functional roles in oocyte meiosis have not been fully determined. RESULTS: We report that CK2 is essential for porcine oocyte meiotic maturation by regulating spindle assembly checkpoint (SAC). Immunostaining and immunoblotting analysis showed that CK2 was constantly expressed and located on the chromosomes during the entire oocyte meiotic maturation. Inhibition of CK2 activity by its selective inhibitor CX-4945 impaired the first polar body extrusion and arrested oocytes at M I stage, accompanied by the presence of BubR1 at kinetochores, indicative of activated SAC. In addition, we found that spindle/chromosome structure was disrupted in CK2-inhibited oocytes due to the weakened microtubule stability, which is a major cause resulting in the activation of SAC. Last, we found that the level DNA damage as assessed by γH2A.X staining was considerably elevated when CK2 was inhibited, suggesting that DNA damage might be another critical factor leading to the SAC activation and meiotic failure of oocytes. CONCLUSIONS: Our findings demonstrate that CK2 promotes the porcine oocyte maturation by ensuring normal spindle assembly and DNA damage repair.
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spelling pubmed-71404932020-04-14 Casein kinase 2 modulates the spindle assembly checkpoint to orchestrate porcine oocyte meiotic progression ShiYang, Xiayan Miao, Yilong Cui, Zhaokang Lu, Yajuan Zhou, Changyin Zhang, Yu Xiong, Bo J Anim Sci Biotechnol Research BACKGROUND: CK2 (casein kinase 2) is a serine/threonine-selective protein kinase that has been involved in a variety of cellular processes such as DNA repair, cell cycle control and circadian rhythm regulation. However, its functional roles in oocyte meiosis have not been fully determined. RESULTS: We report that CK2 is essential for porcine oocyte meiotic maturation by regulating spindle assembly checkpoint (SAC). Immunostaining and immunoblotting analysis showed that CK2 was constantly expressed and located on the chromosomes during the entire oocyte meiotic maturation. Inhibition of CK2 activity by its selective inhibitor CX-4945 impaired the first polar body extrusion and arrested oocytes at M I stage, accompanied by the presence of BubR1 at kinetochores, indicative of activated SAC. In addition, we found that spindle/chromosome structure was disrupted in CK2-inhibited oocytes due to the weakened microtubule stability, which is a major cause resulting in the activation of SAC. Last, we found that the level DNA damage as assessed by γH2A.X staining was considerably elevated when CK2 was inhibited, suggesting that DNA damage might be another critical factor leading to the SAC activation and meiotic failure of oocytes. CONCLUSIONS: Our findings demonstrate that CK2 promotes the porcine oocyte maturation by ensuring normal spindle assembly and DNA damage repair. BioMed Central 2020-04-08 /pmc/articles/PMC7140493/ /pubmed/32292585 http://dx.doi.org/10.1186/s40104-020-00438-1 Text en © The Author(s) 2020 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
ShiYang, Xiayan
Miao, Yilong
Cui, Zhaokang
Lu, Yajuan
Zhou, Changyin
Zhang, Yu
Xiong, Bo
Casein kinase 2 modulates the spindle assembly checkpoint to orchestrate porcine oocyte meiotic progression
title Casein kinase 2 modulates the spindle assembly checkpoint to orchestrate porcine oocyte meiotic progression
title_full Casein kinase 2 modulates the spindle assembly checkpoint to orchestrate porcine oocyte meiotic progression
title_fullStr Casein kinase 2 modulates the spindle assembly checkpoint to orchestrate porcine oocyte meiotic progression
title_full_unstemmed Casein kinase 2 modulates the spindle assembly checkpoint to orchestrate porcine oocyte meiotic progression
title_short Casein kinase 2 modulates the spindle assembly checkpoint to orchestrate porcine oocyte meiotic progression
title_sort casein kinase 2 modulates the spindle assembly checkpoint to orchestrate porcine oocyte meiotic progression
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7140493/
https://www.ncbi.nlm.nih.gov/pubmed/32292585
http://dx.doi.org/10.1186/s40104-020-00438-1
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