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NEK5 regulates cell cycle progression during mouse oocyte maturation and preimplantation embryonic development

Authors :
Zi‐Yun Yi
Lei Guo
Feng Dong
Qing-Yuan Sun
Yi Hou
Zhen-Bo Wang
Zhiming Han
Ying-Chun Ouyang
Hui Li
Yuan‐Yuan Li
Sheng-Sheng Lu
Jian Li
Source :
Molecular Reproduction and Development. 86:1189-1198
Publication Year :
2019
Publisher :
Wiley, 2019.

Abstract

NEK5, a member of never in mitosis-gene A-related protein kinase, is involved in the regulation of centrosome integrity and centrosome cohesion at mitosis in somatic cells. In this study, we investigated the expression and function of NEK5 during mouse oocyte maturation and preimplantation embryonic development. The results showed that NEK5 was expressed from germinal vesicle (GV) to metaphase II (MII) stages during oocyte maturation with the highest level of expression at the GV stage. It was shown that NEK5 localized in the cytoplasm of oocytes at GV stage, concentrated around chromosomes at germinal vesicle breakdown (GVBD) stage, and localized to the entire spindle at prometaphase I, MI and MII stages. The small interfering RNA-mediated depletion of Nek5 significantly increased the phosphorylation level of cyclin-dependent kinase 1 in oocytes, resulting in a decrease of maturation-promoting factor activity, and severely impaired GVBD. The failure of meiotic resumption caused by Nek5 depletion could be rescued by the depletion of Wee1B. We found that Nek5 depletion did not affect CDC25B translocation into the GV. We also found that NEK5 was expressed from 1-cell to blastocyst stages with the highest expression at the blastocyst stage, and Nek5 depletion severely impaired preimplantation embryonic development. This study demonstrated for the first time that NEK5 plays important roles during meiotic G2/M transition and preimplantation embryonic development.

Details

ISSN :
10982795 and 1040452X
Volume :
86
Database :
OpenAIRE
Journal :
Molecular Reproduction and Development
Accession number :
edsair.doi.dedup.....bffd4ec5528d982ecdffbd186f65283e
Full Text :
https://doi.org/10.1002/mrd.23234