The Molecular Mechanism of Aurora-B Regulating Kinetochore-Microtubule Attachment in Mitosis and Oocyte Meiosis

被引:0
|
作者
Chen, Shanshan [1 ]
Sun, Qiqi [1 ]
Yao, Bo [1 ]
Ren, Yanping [1 ]
机构
[1] Zunyi Med Univ, Sch Preclin Med, Dept Histol & Embryol, Zunyi, Peoples R China
基金
中国国家自然科学基金;
关键词
Aurora-B; Oocytes; Meiosis; Mitosis; Kinetochore-microtubule attachment; CHROMOSOME SEGREGATION; MOUSE OOCYTES; HISTONE H3; KINASE; PHOSPHORYLATION; COMPLEX; SURVIVIN; BOREALIN; SPINDLE; INCENP;
D O I
10.1159/000540588
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background: Aurora kinase B (Aurora-B), a member of the chromosomal passenger complex, is involved in correcting kinetochore-microtubule (KT-MT) attachment errors and regulating sister chromatid condensation and cytoplasmic division during mitosis. Summary: However, few reviews have discussed its mechanism in oocyte meiosis and the differences between its role in mitosis and meiosis. Therefore, in this review, we summarize the localization, recruitment, activation, and functions of Aurora-B in mitosis and oocyte meiosis. The accurate regulation of Aurora-B is essential for ensuring accurate chromosomal segregation and correct KT-MT attachments. Aurora-B regulates the stability of KT-MT attachments by competing with cyclin-dependent kinase 1 to control the phosphorylation of the SILK and RVSF motifs on kinetochore scaffold 1 and by competing with protein phosphatase 1 to influence the phosphorylation of NDC80 which is the substrate of Aurora-B. In addition, Aurora-B regulates the spindle assembly checkpoint by promoting the recruitment and activation of mitotic arrest deficient 2. Key Messages: This review provides a theoretical foundation for elucidating the mechanism of cell division and understanding oocyte chromosomal aneuploidy.
引用
收藏
页码:69 / 77
页数:9
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