Kishimoto Takeo
Laboratory of Cell and Developmental Biology, Graduate School of Bioscience, Tokyo Institute of Technology, Nagatsuta 4259, Midoriku, Yokohama 226-8501, Japan.
Curr Opin Cell Biol. 2003 Dec;15(6):654-63. doi: 10.1016/j.ceb.2003.10.010.
The meiotic cell cycle, which is comprised of two consecutive M-phases, is crucial for the production of haploid germ cells. Although both mitotic and meiotic M-phases share cyclin-B-Cdc2/CDK1 as a key controller, there are meiosis-specific modulations in the regulation of cyclin-B-Cdc2. Recent insights indicate that a common pattern in these modulations can be found by considering the particular activities of mitogen-activated protein kinase (MAPK) during meiosis. The G(2)-phase arrest of meiosis I is released via specific, MAPK-independent signalling that leads to cyclin-B-Cdc2 activation; thereafter, however, the meiotic process is under the control of interplay between MAPK and cyclin-B-Cdc2.
减数分裂细胞周期由两个连续的M期组成,对单倍体生殖细胞的产生至关重要。尽管有丝分裂和减数分裂的M期都共享细胞周期蛋白B-Cdc2/CDK1作为关键调控因子,但在细胞周期蛋白B-Cdc2的调控中存在减数分裂特异性调节。最近的研究表明,通过考虑减数分裂期间丝裂原活化蛋白激酶(MAPK)的特定活性,可以发现这些调节中的一个共同模式。减数分裂I的G2期停滞通过特定的、不依赖MAPK的信号传导得以解除,该信号传导导致细胞周期蛋白B-Cdc2激活;然而,此后减数分裂过程受MAPK和细胞周期蛋白B-Cdc2之间相互作用的控制。