Huo Li-Jun, Yu Ling-Zhu, Liang Cheng-Guang, Fan Heng-Yu, Chen Da-Yuan, Sun Qing-Yuan
State Key Laboratory of Reproductive Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, People's Republic of China.
Zygote. 2005 Feb;13(1):45-53. doi: 10.1017/s0967199405003060.
M phase or maturation promoting factor (MPF), a kinase complex composed of the regulatory cyclin B and the catalytic p34cdc2 kinase, plays important roles in meiosis and mitosis. This study was designed to detect and compare the subcellular localization of cyclin B1, phosphorylated cyclin B1 and p34cdc2 during oocyte meiotic maturation and fertilization in mouse. We found that all these proteins were concentrated in the germinal vesicle of oocytes. Shortly after germinal vesicle breakdown, all these proteins were accumulated around the condensed chromosomes. With spindle formation at metaphase I, cyclin B1 and phosphorylated cyclin B1 were localized around the condensed chromosomes and concentrated at the spindle poles, while p34cdc2 was localized in the spindle region. At the anaphase/telophase transition, phosphorylated cyclin B1 was accumulated in the midbody between the separating chromosomes/chromatids, while p34cdc2 was accumulated in the entire spindle except for the midbody region. At metaphase II, both cyclin B1 and p34cdc2 were horizontally localized in the region with the aligned chromosomes and the two poles of the spindle, while phosphorylated cyclin B1 was localized in the two poles of spindle and the chromosomes. We could not detect a particular distribution of cyclin B1 in fertilized eggs when the pronuclei were initially formed, but in late pronuclei cyclin B1 was accumulated in the pronuclei. p34cdc2 and phosphorylated cyclin B1 were always concentrated in one pronucleus after parthenogenetic activation or in two pronuclei after fertilization. At metaphase of 1-cell embryos, cyclin B1 was accumulated around the condensed chromosomes. Cyclin B1 was accumulated in the nucleus of late 2-cell embryos but not in early 2-cell embryos. Furthermore, we also detected the accumulation of p34cdc2 in the nucleus of 2- and 4-cell embryos. All these results show that cyclin B1, phosphorylated cyclin B1 and p34cdc2 have similar distributions at some stages but different localizations at other stages during oocyte meiotic maturation and fertilization, suggesting that they may play a common role in some events but different roles in other events during oocyte maturation and fertilization.
M期或成熟促进因子(MPF)是一种由调节性细胞周期蛋白B和催化性p34cdc2激酶组成的激酶复合物,在减数分裂和有丝分裂中发挥重要作用。本研究旨在检测和比较细胞周期蛋白B1、磷酸化细胞周期蛋白B1和p34cdc2在小鼠卵母细胞减数分裂成熟和受精过程中的亚细胞定位。我们发现所有这些蛋白质都集中在卵母细胞的生发泡中。生发泡破裂后不久,所有这些蛋白质都聚集在浓缩染色体周围。随着减数第一次分裂中期纺锤体的形成,细胞周期蛋白B1和磷酸化细胞周期蛋白B1定位于浓缩染色体周围并集中在纺锤体极,而p34cdc2定位于纺锤体区域。在后期/末期转换时,磷酸化细胞周期蛋白B1聚集在分离的染色体/染色单体之间的中间体中,而p34cdc2聚集在除中间体区域外的整个纺锤体中。在减数第二次分裂中期,细胞周期蛋白B1和p34cdc2都水平定位于染色体排列的区域和纺锤体的两极,而磷酸化细胞周期蛋白B1定位于纺锤体的两极和染色体上。当原核最初形成时,我们在受精卵中未检测到细胞周期蛋白B1的特定分布,但在后期原核中细胞周期蛋白B1聚集在原核中。孤雌激活后,p34cdc2和磷酸化细胞周期蛋白B1总是集中在一个原核中,受精后则集中在两个原核中。在1细胞胚胎的中期,细胞周期蛋白B1聚集在浓缩染色体周围。细胞周期蛋白B1聚集在晚期2细胞胚胎的细胞核中,但早期2细胞胚胎中没有。此外,我们还检测到p34cdc2在2细胞和4细胞胚胎的细胞核中聚集。所有这些结果表明,细胞周期蛋白B1、磷酸化细胞周期蛋白B1和p34cdc2在卵母细胞减数分裂成熟和受精过程中的某些阶段具有相似的分布,但在其他阶段具有不同的定位,这表明它们可能在卵母细胞成熟和受精过程中的某些事件中发挥共同作用,但在其他事件中发挥不同作用。