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Journal of Cell Science
Article . 2004 . Peer-reviewed
Data sources: Crossref
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Suppression ofNek2Ain mouse early embryos confirms its requirement for chromosome segregation

Authors: Kunsoo Rhee; Kyungjin Kim; Inkoo Khang; Seongkeun Sonn;

Suppression ofNek2Ain mouse early embryos confirms its requirement for chromosome segregation

Abstract

Nek2, a mammalian structural homologue of Aspergillus protein kinase NIMA, is predominantly known as a centrosomal kinase that controls centriole-centriole linkage during the cell cycle. However, its dynamic subcellular localization during mitosis suggested that Nek2 might be involved in diverse cell cycle events in addition to the centrosomal cycle. In order to determine the importance of Nek2 during mammalian development, we investigated the expression and function of Nek2 in mouse early embryos. Our results show that both Nek2A and Nek2B were expressed throughout early embryogenesis. Unlike cultured human cells, however, embryonic Nek2A appeared not to be destroyed upon entry into mitosis, suggesting that the Nek2A protein level is controlled in a unique manner during mouse early embryogenesis. Suppression of Nek2 expression by RNAi resulted in developmental defects at the second mitosis. Many of the blastomeres in Nek2-suppressed embryos showed abnormality in nuclear morphology, including dumbbell-like nuclei, nuclear bridges and micronuclei. These results indicate the importance of Nek2 for proper chromosome segregation in embryonic mitoses.

Related Organizations
Keywords

Cell Nucleus, Centrosome, Chromosome Aberrations, Male, Down-Regulation, Embryonic Development, Gene Expression Regulation, Developmental, Mitosis, RNA Ligase (ATP), Spindle Apparatus, Protein Serine-Threonine Kinases, Embryo, Mammalian, Mice, Chromosome Segregation, Animals, NIMA-Related Kinases, Protein Isoforms, Female, RNA, Double-Stranded

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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
30
Top 10%
Top 10%
Top 10%
bronze