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Abstract
Aurora-A is a serine/threonine protein kinase that plays a
role in cell cycle regulation. The activity of this kinase
has been shown to be required for regulating multiple
stages of mitotic progression in somatic cells. In this
study, the changes in Aurora-A expression were revealed in
mouse oocytes using Western blotting. The subcellular
localization of Aurora-A during oocyte meiotic maturation,
fertilization and early cleavages as well as after
antibody microinjection or microtubule assembly
perturbance was studied with confocal microscopy. The
quantity of Aurora-A protein was high in the germinal
vesicle (GV) and metaphase II (MII) oocytes and remained
stable during other meiotic maturation stages. Aurora-A
concentrated in the GV before meiosis resumption, in the
pronuclei of fertilized eggs, and in the nuclei of early
embryo blastomeres. Aurora-A was localized to the spindle
poles of the meiotic spindle from the metaphase I (MI)
stage to metaphase II stage. During early embryo
development, Aurora-A was found in association with the
mitotic spindle poles. Aurora-A was not found in the
spindle region when colchicine or staurosporine was used
to inhibit microtubule organization, while it accumulated
as several dots in the cytoplasm after taxol treatment.
Aurora-A antibody microinjection decreased the rate of
germinal vesicle breakdown (GVBD) and distorted MI spindle
organization. Our results indicate that Aurora-A is a
critical regulator of cell cycle progression and
microtubule organization during mouse oocyte meiotic
maturation, fertilization and early embryo cleavage.
Key words:
Gamete Biology
Early development
Fertilization
Meiosis
Ovum
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