绵羊卵母细胞生发囊泡破裂所需的蛋白质。

R M Moor, I M Crosby
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引用次数: 0

摘要

通过分析过渡阶段的蛋白质变化和引入蛋白质块,研究了从前期到中期的细胞周期调控。结果表明,羊卵母细胞向中期的发展完全依赖于新蛋白的合成。通过在减数分裂恢复后逐渐延长抑制剂环己亚胺的添加时间,可以确定所需的合成发生在生发囊泡破裂(GVBD)之前的1-2小时。环己亚胺的作用是完全可逆的:在3至4小时后,药物的去除导致GVBD。通过对卵母细胞进行[35S]蛋氨酸和[32P]磷酸盐的短期放射性标记,然后快速评估其精确的核构型,研究了成熟最初几个小时内蛋白质的合成和修饰。培养开始后4-5小时检测到两种多肽磷酸化的变化,但这些变化不依赖于蛋白质合成。最早的合成变化是在离体后6-8小时,即GVBD前出现新的多肽。该多肽(Mr为47 X 10(3), pI为5.8)未被显著磷酸化,且相对稳定。经环己亚胺处理后释放的卵母细胞在3-4小时后开始合成该分子,再次与GVBD相吻合。α -amanitin抑制转录抑制了多肽的合成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Protein requirements for germinal vesicle breakdown in ovine oocytes.

The regulation of the cell cycle during the transition from prophase to metaphase I was studied by analysing protein changes and introducing protein blocks during the transition phase. The results show that the progression to metaphase in ovine oocytes is totally dependent on new protein synthesis. By delaying the addition of the inhibitor, cycloheximide, for progressively longer periods after the resumption of meiosis it was established that the required synthesis occurs in the 1-2 h immediately preceding germinal vesicle breakdown (GVBD). The action of cycloheximide was fully reversible: removal of the drug resulted in GVBD between 3 and 4 h later. The synthesis and modification of proteins during these first few hours of maturation were studied by short-term radiolabelling of oocytes with [35S]methionine and [32P]phosphate followed by rapid assessment of their precise nuclear configuration. Changes in phosphorylation of two polypeptides were detected 4-5 h after the beginning of culture, but these changes were not dependent upon protein synthesis. The earliest change in synthesis was the appearance of a new polypeptide 6-8 h after explantation, immediately before GVBD. This polypeptide (Mr 47 X 10(3), pI 5.8) was not significantly phosphorylated and was relatively stable. Oocytes released from cycloheximide treatment began to synthesize this molecule 3-4 h later, again coinciding with GVBD. Synthesis of the polypeptide was suppressed by inhibition of transcription with alpha-amanitin.

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