Abrieu A, Dorée M, Fisher D
Ludwig Institute for Cancer Research, UCSD, La Jolla, California 92093-0660, USA.
J Cell Sci. 2001 Jan;114(Pt 2):257-67. doi: 10.1242/jcs.114.2.257.
Throughout oocyte maturation, and subsequently during the first mitotic cell cycle, the MAP kinase cascade and cyclin-B-Cdc2 kinase are associated with the control of cell cycle progression. Many roles have been directly or indirectly attributed to MAP kinase and its influence on cyclin-B-Cdc2 kinase in different model systems; yet a principle theme does not emerge from the published literature, some of which is apparently contradictory. Interplay between these two kinases affects the major events of meiotic maturation throughout the animal kingdom, including the suppression of DNA replication, the segregation of meiotic chromosomes, and the prevention of parthenogenetic activation. Central to many of these events appears to be the control by MAP kinase of cyclin translation and degradation.
在整个卵母细胞成熟过程中,以及随后的第一次有丝分裂细胞周期中,丝裂原活化蛋白激酶(MAP激酶)级联反应和细胞周期蛋白B-Cdc2激酶与细胞周期进程的控制相关。在不同的模型系统中,MAP激酶直接或间接地发挥了许多作用,并对细胞周期蛋白B-Cdc2激酶产生影响;然而,已发表的文献并未呈现出一个主要的主题,其中一些内容显然相互矛盾。这两种激酶之间的相互作用影响着整个动物界减数分裂成熟的主要事件,包括DNA复制的抑制、减数分裂染色体的分离以及孤雌生殖激活的预防。许多这些事件的核心似乎是MAP激酶对细胞周期蛋白翻译和降解的控制。