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脊索动物CDK1旁系同源物在卵子发生减数分裂过程中的功能特化。

Functional specialization of chordate CDK1 paralogs during oogenic meiosis.

作者信息

Øvrebø Jan Inge, Campsteijn Coen, Kourtesis Ioannis, Hausen Harald, Raasholm Martina, Thompson Eric M

机构信息

a Department of Biology ; University of Bergen ; Bergen , Norway.

出版信息

Cell Cycle. 2015;14(6):880-93. doi: 10.1080/15384101.2015.1006000.

Abstract

Cyclin-dependent kinases (CDKs) are central regulators of eukaryotic cell cycle progression. In contrast to interphase CDKs, the mitotic phase CDK1 is the only CDK capable of driving the entire cell cycle and it can do so from yeast to mammals. Interestingly, plants and the marine chordate, Oikopleura dioica, possess paralogs of the highly conserved CDK1 regulator. However, whereas in plants the 2 CDK1 paralogs replace interphase CDK functions, O. dioica has a full complement of interphase CDKs in addition to its 5 odCDK1 paralogs. Here we show specific sub-functionalization of odCDK1 paralogs during oogenesis. Differential spatiotemporal dynamics of the odCDK1a, d and e paralogs and the meiotic polo-like kinase 1 (Plk1) and aurora kinase determine the subset of meiotic nuclei in prophase I arrest that will seed growing oocytes and complete meiosis. Whereas we find odCDK1e to be non-essential, knockdown of the odCDK1a paralog resulted in the spawning of non-viable oocytes of reduced size. Knockdown of odCDK1d also resulted in the spawning of non-viable oocytes. In this case, the oocytes were of normal size, but were unable to extrude polar bodies upon exposure to sperm, because they were unable to resume meiosis from prophase I arrest, a classical function of the sole CDK1 during meiosis in other organisms. Thus, we reveal specific sub-functionalization of CDK1 paralogs, during the meiotic oogenic program.

摘要

细胞周期蛋白依赖性激酶(CDKs)是真核细胞周期进程的核心调节因子。与间期CDKs不同,有丝分裂期的CDK1是唯一能够驱动整个细胞周期的CDK,并且从酵母到哺乳动物都能如此。有趣的是,植物和海洋脊索动物住囊虫(Oikopleura dioica)拥有高度保守的CDK1调节因子的旁系同源物。然而,在植物中,两个CDK1旁系同源物取代了间期CDK的功能,而住囊虫除了其5个odCDK1旁系同源物外,还拥有完整的间期CDKs。在这里,我们展示了odCDK1旁系同源物在卵子发生过程中的特定亚功能化。odCDK1a、d和e旁系同源物以及减数分裂的polo样激酶1(Plk1)和极光激酶的不同时空动态决定了减数分裂前期I停滞的减数分裂细胞核子集,这些细胞核将为生长中的卵母细胞提供种子并完成减数分裂。虽然我们发现odCDK1e并非必需,但敲低odCDK1a旁系同源物会导致产出大小减小的无活力卵母细胞。敲低odCDK1d也会导致产出无活力的卵母细胞。在这种情况下,卵母细胞大小正常,但在接触精子时无法排出极体,因为它们无法从减数分裂前期I停滞中恢复减数分裂,而这是其他生物体中唯一的CDK1在减数分裂期间的经典功能。因此,我们揭示了在减数分裂卵子发生程序中CDK1旁系同源物的特定亚功能化。

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