Abrieu A, Fisher D, Simon M N, Dorée M, Picard A
Centre de Recherches de Biochimie Macromoléculaire, Montpellier, France.
EMBO J. 1997 Nov 3;16(21):6407-13. doi: 10.1093/emboj/16.21.6407.
Down-regulation of MAP kinase (MAPK) is a universal consequence of fertilization in the animal kingdom, although its role is not known. Here we show that MAPK inactivation is essential for embryos, both vertebrate and invertebrate, to enter first mitosis. Suppressing down-regulation of MAPK at fertilization, for example by constitutively activating the upstream MAPK cascade, specifically suppresses cyclin B-cdc2 kinase activation and its consequence, entry into first mitosis. It thus appears that MAPK functions in meiotic maturation by preventing unfertilized eggs from proceeding into parthenogenetic development. The most general effect of artificially maintaining MAPK activity after fertilization is prevention of the G2 to M-phase transition in the first mitotic cell cycle, even though inappropriate reactivation of MAPK after fertilization may lead to metaphase arrest in vertebrates. Advancing the time of MAPK inactivation in fertilized eggs does not, however, speed up their entry into first mitosis. Thus, sustained activity of MAPK during part of the first mitotic cell cycle is not responsible for late entry of fertilized eggs into first mitosis.
丝裂原活化蛋白激酶(MAPK)的下调是动物界受精的普遍结果,尽管其作用尚不清楚。在这里,我们表明MAPK失活对于脊椎动物和无脊椎动物胚胎进入第一次有丝分裂至关重要。例如,通过组成性激活上游MAPK级联反应来抑制受精时MAPK的下调,会特异性地抑制细胞周期蛋白B - cdc2激酶的激活及其进入第一次有丝分裂的结果。因此,MAPK似乎通过防止未受精卵进入孤雌生殖发育来发挥减数分裂成熟的作用。受精后人为维持MAPK活性的最普遍影响是阻止第一个有丝分裂细胞周期中从G2期到M期的转变,尽管受精后MAPK的不适当重新激活可能导致脊椎动物中期停滞。然而,提前受精卵中MAPK失活的时间并不会加速它们进入第一次有丝分裂。因此,在第一个有丝分裂细胞周期的部分时间内MAPK的持续活性并不是受精卵延迟进入第一次有丝分裂的原因。