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Nek2 and its substrate, centrobin/Nip2, are required for proper meiotic spindle formation of the mouse oocytes

Published online by Cambridge University Press:  23 June 2010

Seongkeun Sonn
Affiliation:
Division of Life and Pharmaceutical Sciences, Ewha Womans University, Seoul 120–750, Korea.
Goo Taeg Oh
Affiliation:
Division of Life and Pharmaceutical Sciences, Ewha Womans University, Seoul 120–750, Korea.
Kunsoo Rhee*
Affiliation:
Department of Biological Sciences, Seoul National University, Seoul, 151–747, Korea.
*
All correspondence to: Kunsoo Rhee. Department of Biological Sciences, Seoul National University, Seoul, 151–747, Korea. Tel: +82 2 880 5751. Fax: +82 2 873 5751. e-mail: rheek@snu.ac.kr

Summary

A typical centrosome consists of a pair of centrioles embedded in a proteinous matrix called pericentriolar material. However, the centrosomes in the mouse oocytes and early embryos lack centrioles, but consist of the γ-tubulin-enriched vesicle aggregates. We previously revealed that Nek2 and centrobin/Nip2, a centrosomal substrate of Nek2, is critical for the mouse early embryogenesis, especially at the step of spindle assembly during mitosis. In order to expand our understanding of the biological functions of Nek2, we examined expression and knockdown phenotypes of Nek2 and its substrates, centrobin and C-Nap1, in the mouse oocyte. Nek2, centrobin and C-Nap1 in the mouse oocytes were also centrosomal. Suppression of Nek2 and its substrates did not affect meiotic resumption of the oocytes. However, meiosis of the Nek2- and centrobin-suppressed oocytes was not completed, but arrested with defects in spindle assembly. No visible phenotype was observed in the C-Nap1-suppressed oocytes. These results indicate that Nek2 is critical for proper assembly of the meiotic spindles. Centrobin may be a possible substrate of Nek2 responsible for the meiotic spindle assembly in the mouse oocytes.

Type
Research Article
Copyright
Copyright © Cambridge University Press 2010

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