Gautier J, Beetschen J C
Dev Biol. 1985 Jul;110(1):192-9. doi: 10.1016/0012-1606(85)90075-2.
It has been shown that various inhibitors of protein synthesis can elicit the precocious appearance of a gray crescent (GC) in in vitro maturing, nonactivated Ambystoma mexicanum oocytes. However, evidence has now been obtained that these treatments fail to induce GC formation when the oocytes are enucleated before initiation of maturation. The ability to form a GC is reestablished in enucleated oocytes by the injection of nucleoplasm from a normal oocyte, either before or after the injection of the inhibitor. In the latter case, the GC appears very rapidly, even though protein synthesis is at about 1/10th that of the control enucleated oocyte, after treatment with diphtheria toxin (final concentration 10(-8) M) as an inhibitor. One or several nuclear factors, in conjunction with inhibition of protein synthesis, are therefore essential for early symmetrization. The corrective nuclear factor is already present in the germinal vesicle of young oocytes, at the very beginning of vitellogenesis. It is not species specific, since enucleated axolotl oocytes can be symmetrized with Pleurodeles or even Xenopus oocyte nucleoplasm. Moreover, it has been shown that the nuclear-cytoplasmic interaction is possible only when cytoplasmic maturation has been proceeding for at least 10 hr after exposure to progesterone (at 18 degrees C). A three-step process as a prerequisite of GC formation in the oocyte is proposed: Cytoplasmic maturation must proceed till a reactive state is attained, allowing interactions with nuclear factors; Nuclear factor(s) interact(s) with matured cytoplasm; Inhibition of protein synthesis triggers GC formation. Sequence of steps 2 and 3 can be experimentally inverted but must always be preceded by step 1. Since a sharp reduction in amino acid incorporation has also been found in normally fertilized eggs just prior to GC formation, it is suggested that the scheme described above could be also applicable to normal symmetrization in this model system.
已经表明,各种蛋白质合成抑制剂可在体外成熟、未激活的美西钝口螈卵母细胞中引发灰色新月体(GC)的早熟出现。然而,现在有证据表明,当卵母细胞在成熟开始前去核时,这些处理无法诱导GC形成。通过在注射抑制剂之前或之后注射正常卵母细胞的核质,去核卵母细胞重新获得了形成GC的能力。在后一种情况下,即使在用白喉毒素(终浓度10(-8)M)作为抑制剂处理后,蛋白质合成仅为对照去核卵母细胞的约1/10,GC也会非常迅速地出现。因此,一种或几种核因子与蛋白质合成的抑制相结合,对于早期对称化是必不可少的。校正性核因子在卵黄发生刚开始时就已存在于年轻卵母细胞的生发泡中。它不是物种特异性的,因为去核的美西螈卵母细胞可以与肋突螈甚至非洲爪蟾卵母细胞核质实现对称化。此外,已经表明,只有当细胞质在暴露于孕酮(18℃)后至少进行10小时的成熟时,核质相互作用才可能发生。提出了一个三步过程作为卵母细胞中GC形成的先决条件:细胞质成熟必须进行到达到反应状态,允许与核因子相互作用;核因子与成熟的细胞质相互作用;蛋白质合成的抑制触发GC形成。步骤2和3的顺序可以通过实验颠倒,但必须始终以步骤1为前提。由于在正常受精的卵中,就在GC形成之前也发现氨基酸掺入急剧减少,因此表明上述方案也可能适用于该模型系统中的正常对称化。