Fisher D, Abrieu A, Simon M N, Keyse S, Vergé V, Dorée M, Picard A
CRBM CNRS ERS 155, 1919 route de mende, Montpellier cedex 5, 34293, France.
Dev Biol. 1998 Oct 1;202(1):1-13. doi: 10.1006/dbio.1998.8981.
Downregulation of MAP kinase is a universal consequence of fertilization in the animal kingdom. Here we show that oocytes of the starfishes Astropecten aranciacus and Marthasterias glacialis complete meiotic maturation and form a pronucleus when treated with 1-methyladenine and then complete DNA replication and arrest at G2 if not fertilized. Release of G2 by fertilization or a variety of parthenogenetic treatments is associated with inactivation of MAP kinase. Prevention of MAP kinase inactivation by microinjection of Ste11-DeltaN, a constitutively active budding yeast MAP kinase kinase kinase, arrests fertilized eggs at G2 in either the first or the second mitotic cell cycle, in a dose-dependent manner. G1 arrest is never observed. Conversely, inactivation of MAP kinase by microinjection of the MAP kinase-specific phosphatase Pyst-1 releases mature starfish oocytes from G2 arrest. The role of MAP kinase in arresting cell cycle at various stages in oocytes of different animal species is discussed.
丝裂原活化蛋白激酶(MAP激酶)的下调是动物界受精的普遍结果。在此我们表明,用1-甲基腺嘌呤处理时,橙黄海星(Astropecten aranciacus)和冰川多棘海盘车(Marthasterias glacialis)的卵母细胞完成减数分裂成熟并形成原核,然后如果未受精则完成DNA复制并停滞在G2期。受精或各种孤雌生殖处理导致的G2期解除与MAP激酶的失活相关。通过显微注射组成型活性出芽酵母丝裂原活化蛋白激酶激酶激酶Ste11-DeltaN来防止MAP激酶失活,会使受精卵在第一个或第二个有丝分裂细胞周期的G2期停滞,且呈剂量依赖性。从未观察到G1期停滞。相反,通过显微注射MAP激酶特异性磷酸酶Pyst-1使MAP激酶失活,可使成熟海星卵母细胞从G2期停滞中解除。本文讨论了MAP激酶在不同动物物种卵母细胞的各个阶段阻止细胞周期中的作用。