Josefsberg Liat Ben-Yehoshua, Galiani Dalia, Lazar Shlomi, Kaufman Orit, Seger Rony, Dekel Nava
Department of Biological Regulation, The Weizmann Institute of Science, Rehovot 76100, Israel.
Biol Reprod. 2003 Apr;68(4):1282-90. doi: 10.1095/biolreprod.102.006882. Epub 2002 Oct 30.
Meiosis is a particular example of a cell cycle, characterized by two successive divisions without an intervening interphase. Resumption of meiosis in oocytes is associated with activation of maturation-promoting factor (MPF) and mitogen-activated protein kinase (MAPK). The activity of MPF declines during the transition between the two meiotic divisions, whereas the activity of MAPK is sustained. Attempts to disclose the interplay between these key regulators of meiosis in both amphibian and mammalian oocytes generated contradictory results. Furthermore, the enzyme that governs the suppression of interphase in mammals is still unidentified. To our knowledge, we provide herein the first demonstration in a mammalian system that inhibition of MPF at reinitiation of meiosis abrogated Mos expression and MAPK activation. We also show that oocytes, in which reactivation of MPF at completion of the first telophase was prevented, exhibited an interphase nucleus with decondensed chromosomes. Inhibition of MAPK did not interfere with the progression to the second meiotic metaphase but, rather, resulted in parthenogenic activation. We conclude that in rat oocytes, MPF regulates MAPK activation and its timely reactivation prevents the oocytes from entering interphase.
减数分裂是细胞周期的一个特殊例子,其特征是连续两次分裂,中间没有间期。卵母细胞减数分裂的恢复与成熟促进因子(MPF)和丝裂原活化蛋白激酶(MAPK)的激活有关。MPF的活性在两次减数分裂之间的过渡阶段下降,而MAPK的活性则持续存在。在两栖动物和哺乳动物卵母细胞中,试图揭示这些减数分裂关键调节因子之间相互作用的研究产生了相互矛盾的结果。此外,在哺乳动物中控制间期抑制的酶仍未确定。据我们所知,我们在此首次在哺乳动物系统中证明,减数分裂重新启动时抑制MPF可消除Mos表达和MAPK激活。我们还表明,在第一次末期完成时阻止MPF重新激活的卵母细胞表现出具有解聚染色体的间期细胞核。抑制MAPK并不干扰向第二次减数分裂中期的进程,而是导致孤雌激活。我们得出结论,在大鼠卵母细胞中,MPF调节MAPK激活,其及时重新激活可防止卵母细胞进入间期。