蛋白酶、受精或离子载体A 23187诱导的减数分裂重新开始时,刺激肺泡Sabellaria alveolata(多毛纲环节动物)卵母细胞内源性蛋白磷酸化

G. Peaucellier, M. Dorée, J. Demaille
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引用次数: 25

摘要

当特定蛋白酶刺激Sabellaria卵母细胞从前期I阻断持续到中期I阻断时,[32P]-磷酸盐在蛋白中的掺入增强。从开始治疗到生发囊泡破裂(GVB),掺入率增加了50倍。当前期阻滞释放涉及施肥或离子载体a23187激活时,结果相同。在所有情况下,减数分裂都与18000道尔顿蛋白的磷酸化有关,这可能在前驱阻滞的卵母细胞中没有标记。完整卵母细胞中主要磷酸化蛋白之一的38,000-40,000道尔顿膜蛋白双偶体的磷酸化,在卵母细胞释放前期阻滞后制备的匀浆中也被强烈增强。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Stimulation of endogenous protein phosphorylation in oocytes of Sabellaria alveolata (polychaete annelid) at meiosis reinitiation induced by protease, fertilization, or ionophore A 23187
Incorporation of [32P]-phosphate into proteins was enhanced when Sabellaria oocytes were stimulated with specific protease to continue from prophase I block to metaphase I block. The rate of incorporation was increased 50 fold between onset of treatment and germinal vesicle breakdown (GVB). The same result was obtained when release from prophase block involved fertilization, or activation with ionophore A 23187. In all cases, meiosis was associated with phosphorylation of an 18,000 dalton protein, which is perhaps not labeled in prophase-blocked oocytes. Phosphorylation of a 38,000–40,000 dalton doublet of membrane proteins, which are among the main phosphorylated proteins in intact oocytes, was also strongly enhanced in vitro in homogenates prepared from oocytes following release from prophase block.
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