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Meiotic cell cycle control by mos in ascidian oocytes

机译:减数分裂细胞周期由MOS在阿霉卵ytes中控制

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Mitotic cell division cycle is regulated by several control mechanisms generally known as checkpoints, whose main function is to ensure that critical events in the cell division such as DNA replication and chromosome segregation occur with high fidelity and in the correct order and time. A recent view of cell cycle regulation, indicate that check-points work as signal transduction pathways with their initiating, signals, sensors, transducers, and effectors (Elledge, 1996). Similarly, meiotic cell cycle regulation have specific checkpoints and two of them have been recently characterized at molecular level. The first ensures the completion of recombination before the formation of meiosis I spindle; the second blocks anaphase I until all the paired chromosomes are correctly attached to the spindle (Page and Orr-Weaver, 1997). However, he most intriguing difference between mitosis and meiosis respect to cell cycle regulation, is the ability of animal oocytes to arrest at specific stage during maturation, and maintain this block for extremely long time: from years frog) to decades (human) (Sagata, 1996a,b). It is universally accepted that the meiotic block is due to the activity of a cytostatic factor (CSF) primarily identified by Masui (Masui and Markert, 1971).
机译:有丝分裂细胞分裂周期由通常称为检查点的几种控制机制调节,其主要功能是确保细胞分裂中的临界事件如DNA复制和染色体隔离,以高保真和正确的顺序和时间发生。最近对细胞周期调节的看法,表明检查点用作信号转导途径,其启动,信号,传感器,换能器和效果(EllEdge,1996)。类似地,减数分裂细胞周期调节具有特定的检查点,最近在分子水平上表征了其中的两个。首先确保在MeIosis的形成之前完成重组;第二块嵌入后,直到所有配对的染色体都正确连接到主轴(页面和织布瓦,1997)。然而,有丝分裂和分裂症之间的最有趣的差异是细胞周期调节,是动物卵母细胞在成熟期间在特定阶段逮捕的能力,并将这一块保持非常长的时间:从几年的青蛙到几十年(人类)(佐历,1996A,B)。普遍认为,减数分裂块是由于主要由Masui(Masui和Markert,1971)鉴定的细胞抑制因子(CSF)的活性。

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