在四膜虫的同步细胞周期中,多体上的微管蛋白mRNA的丰度。

R C Bird, A M Zimmerman
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引用次数: 3

摘要

以原生动物梨形四膜虫(Tetrahymena pyriformis GL)为模型系统,研究细胞周期和纤毛再生过程中的多体mRNA。我们之前的工作已经表明,微管蛋白的合成在脱链后和同步细胞周期的G2期间有实质性的诱导作用。在本研究中,我们检测了多聚体上微管蛋白mRNA的丰度,以确定在微管蛋白合成高峰期是否有更多的微管蛋白mRNA被翻译。在小麦胚芽的无细胞翻译系统中,分离的多聚体在脱解后的连续时间和同步细胞周期中被翻译。多体上微管蛋白mRNA的丰度是通过体外微管蛋白的翻译量来推断的。在脱脂后和微管蛋白合成高峰期之前,微管蛋白mRNA的丰度(在脱脂后140分钟)增加到初始值(在脱脂后20分钟)的25倍。由于微管蛋白mRNA丰度的增加先于微管蛋白合成的峰值,因此微管蛋白合成的诱导似乎依赖于mRNA。对同步细胞周期多体上的微管蛋白mRNA丰度的类似分析显示,微管蛋白mRNA的峰值先于每个微管蛋白合成峰值。这些研究表明,微管蛋白合成的周期性波动依赖于多体上微管蛋白mRNA水平的波动。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Abundance of tubulin mRNA on polysomes following deciliation and during the synchronous cell cycle of Tetrahymena.

The protozoan, Tetrahymena pyriformis GL, was used as a model system for studying polysomal mRNA during the cell cycle and during cilia regeneration. Our previous work has shown a substantial induction of tubulin synthesis following deciliation and during G2 of the synchronous cell cycle. In the present study, the abundance of tubulin mRNA on polysomes was examined in order to determine whether more tubulin mRNA was being translated during the periods of peak tubulin synthesis. Polysomes isolated at sequential times following deciliation and during the synchronous cell cycle were translated in a cell-free translation system derived from wheat germ. The abundance of tubulin mRNA on polysomes was inferred from the amount of tubulin translated in vitro. Following deciliation and prior to the peak period of tubulin synthesis, the abundance of tubulin mRNA (at 140 min post-deciliation) increases to 25 times the initial value observed (at 20 min post-deciliation). Since the increase in tubulin mRNA abundance precedes the peak in tubulin synthesis, induction of tubulin synthesis appears to be mRNA-dependent. A similar analysis of tubulin mRNA abundance on polysomes during the synchronous cell cycle revealed a peak of tubulin mRNA prior to each peak of tubulin synthesis. These studies suggest that the periodic fluctuations in the synthesis of tubulin are dependent upon fluctuating levels of tubulin mRNA on polysomes.

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