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一种控制核膜破裂的细胞质因子的周期性行为。

The cyclic behavior of a cytoplasmic factor controlling nuclear membrane breakdown.

作者信息

Wasserman W J, Smith L D

出版信息

J Cell Biol. 1978 Jul;78(1):R15-22. doi: 10.1083/jcb.78.1.r15.

Abstract

The activity of a cytoplasmic factor (MPF), capable of inducing nuclear membrane breakdown (germinal vesicle breakdown) when injected into amphibian oocytes, has been studied during the course of early cleavage in amphibian embryos. Mature egg cytoplasm was found to contain high levels of this activity, but this was quickly lost after fertilization or artificial activation. MPF activity later reappeared in the egg cytoplasm and started to cycle with time. The peak of embryonic MPF activity during each cycle coincided with the time the embryonic nuclei were entering the G2-M transition, i.e., mitosis. However, in colchicine-arrested embryos, this activity remained at an elevated level and no longer oscillated. The timing of the appearance and disappearance of this activity appeared to be under the control of the cytoplasm because such behavior was still observed in enucleated eggs. Continued protein synthesis in the embryo was required for the reappearance, but not for the disappearance, of this activity. MPF, previously thought to be restricted to oocyte maturation, may play a more general role in controlling nuclear membrane breakdown during mitosis as well as meiosis.

摘要

一种细胞质因子(MPF),当注入两栖类卵母细胞时能够诱导核膜破裂(生发泡破裂),其活性已在两栖类胚胎早期卵裂过程中得到研究。发现成熟卵细胞质中含有高水平的这种活性,但受精或人工激活后这种活性很快丧失。MPF活性随后在卵细胞质中重新出现并开始随时间循环。每个周期中胚胎MPF活性的峰值与胚胎细胞核进入G2-M转换期(即有丝分裂期)的时间一致。然而,在秋水仙碱阻滞的胚胎中,这种活性保持在较高水平且不再振荡。这种活性出现和消失的时间似乎受细胞质控制,因为在去核卵中仍观察到这种行为。胚胎中MPF活性的重新出现需要持续的蛋白质合成,但活性的消失则不需要。MPF以前被认为仅限于卵母细胞成熟,可能在控制有丝分裂以及减数分裂期间的核膜破裂中发挥更普遍的作用。

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