Weber M, Kubiak J Z, Arlinghaus R B, Pines J, Maro B
Laboratoire de Physiologie du Développement, Université Paris VII, France.
Dev Biol. 1991 Nov;148(1):393-7. doi: 10.1016/0012-1606(91)90347-6.
Recently, it has been shown that the product of the c-mos proto-oncogene is a component of cytostatic factor, an activity present in unfertilized eggs from vertebrates that arrests the cell cycle in metaphase of the second meiotic division (metaphase II) possibly by stabilizing maturation-promoting factor (MPF). We have studied the behavior of the c-mos product in metaphase II mouse oocytes and soon after activation. The amount of c-mos in the oocyte was still very high after second polar body extrusion, when cyclin B has been degraded and MPF activity had decreased dramatically. Degradation of c-mos takes place later, during the G1 phase of the first cell cycle and a residual amount of c-mos is detectable during the first zygotic interphase. Our data show that the degradation of c-mos is not involved in the release from the metaphase arrest.
最近研究表明,原癌基因c-mos的产物是细胞静止因子的一个组成部分,这种活性存在于脊椎动物未受精卵中,可能通过稳定促成熟因子(MPF)使细胞周期停滞在第二次减数分裂中期(中期II)。我们研究了中期II小鼠卵母细胞及激活后不久c-mos产物的行为。在第二极体排出后,卵母细胞中c-mos的量仍然很高,此时周期蛋白B已降解,MPF活性显著降低。c-mos的降解发生在稍后的第一个细胞周期的G1期,并且在第一次合子间期可检测到c-mos的残留量。我们的数据表明,c-mos的降解与从中期停滞状态释放无关。