Chesnel Franck, Vignaux Françoise, Richard-Parpaillon Laurent, Huguet Antoine, Kubiak Jacek Z
UMR 6061 CNRS, Biology and Genetics of Development, Mitosis and Meiosis Group, IFR140 GFAS, University of Rennes 1, Faculty of Medicine, 2 Ave. Prof. Léon Bernard, CS 34317, 35043 Rennes cedex, France.
Dev Biol. 2005 Sep 15;285(2):358-75. doi: 10.1016/j.ydbio.2005.06.028.
The first embryonic M-phase is special, being the time when paternal and maternal chromosomes mix together for the first time. Reports from a variety of species suggest that the regulation of first M-phase has many particularities; however, no systematic comparative study of the biochemical aspects of first and the following M-phases has been previously undertaken. Here, we ask whether the regulation of the first embryonic M-phase is modified, using Xenopus cell-free extracts. We developed new types of extract specific for the first and the second M-phase obtained either from parthenogenetic or from in vitro fertilized embryos. Analyses of these extracts confirmed that the amplitude of histone H1 kinase activity reflecting CDK1/cyclin B (or MPF for M-phase Promoting Factor) activity is higher and persists longer than during the second M-phase, and that levels of cyclins B1 and B2 are correspondingly higher during the first than the second embryonic M-phase. Inhibition of protein synthesis shortly before M-phase entry reduced mitotic histone H1 kinase amplitude, shortened the period of mitotic phosphorylation of chosen marker proteins, and reduced cyclin B1 and B2 levels, suggesting a role of B-type cyclins in regulating the duration of mitotic events. Moreover, addition of exogenous cyclin B to the extract prior the second mitosis brought forward the activation of mitotic histone H1 kinase but prolonged the duration of this activity. We also confirmed that the inhibitory phosphorylation of CDK1 on tyrosine 15 oscillates between the first two embryonic M-phases, but is clearly more pronounced before the first than the second mitosis, while the MAP kinase ERK2 tended to show greater activation during the first embryonic M-phase but with a similar duration of activation. We conclude that discrete differences exist between the first two M-phases in Xenopus embryo and that higher CDK1/cyclin B activity and B-type cyclin levels could account for the different characteristics of these M-phases.
第一次胚胎M期很特殊,是父本和母本染色体首次混合的时期。来自多种物种的报告表明,第一次M期的调控有许多特殊性;然而,此前尚未对第一次和后续M期的生化方面进行系统的比较研究。在此,我们利用非洲爪蟾无细胞提取物来探究第一次胚胎M期的调控是否存在差异。我们开发了从孤雌生殖或体外受精胚胎中获得的、分别针对第一次和第二次M期的新型提取物。对这些提取物的分析证实,反映CDK1/细胞周期蛋白B(或促M期因子MPF)活性的组蛋白H1激酶活性幅度比第二次M期更高且持续时间更长,并且在第一次胚胎M期细胞周期蛋白B1和B2的水平相应地高于第二次。在进入M期前不久抑制蛋白质合成会降低有丝分裂组蛋白H1激酶幅度,缩短所选标记蛋白的有丝分裂磷酸化时期,并降低细胞周期蛋白B1和B2水平,这表明B型细胞周期蛋白在调节有丝分裂事件持续时间中起作用。此外,在第二次有丝分裂之前向提取物中添加外源细胞周期蛋白B会提前有丝分裂组蛋白H1激酶的激活,但延长了该活性的持续时间。我们还证实,CDK1在酪氨酸15位点的抑制性磷酸化在头两个胚胎M期之间振荡,但在第一次有丝分裂之前比第二次更明显,而丝裂原活化蛋白激酶ERK2在第一次胚胎M期倾向于表现出更大的激活,但激活持续时间相似。我们得出结论,非洲爪蟾胚胎的头两个M期之间存在明显差异,并认为较高的CDK1/细胞周期蛋白B活性和B型细胞周期蛋白水平可以解释这些M期的不同特征。