Carrino J J, Laffler T G
J Cell Biol. 1985 Feb;100(2):642-7. doi: 10.1083/jcb.100.2.642.
In the myxomycete Physarum polycephalum, tubulin synthesis is subject to mitotic cycle control. Virtually all tubulin synthesis is limited to a 2-h period immediately preceding mitosis, and the peak of tubulin protein synthesis is accompanied by a parallel increase in the level of tubulin mRNA. The mechanism by which the accumulation of tubulin mRNA is turned on and off is not clear. To probe the relationship between tubulin regulation and cell cycle controls, we have used heat shocks to delay mitosis and have followed the pattern of tubulin synthesis during these delays. Two peaks of tubulin synthesis are observed after a heat shock. One occurs at a time when synthesis would have occurred without a heat shock, and a second peak immediately precedes the eventual delayed mitosis. These results are clearly due to altered cell cycle regulation. No mitotic activity is detected in delayed plasmodia at the time of the control mitosis, and tubulin behavior is shown to be clearly distinct from that of heat shock proteins. We believe that the tubulin family of proteins is subject to regulation by a thermolabile mitotic control mechanism but that once the cell has been committed to a round of tubulin synthesis the "tubulin clock" runs independently of the heat sensitive system. In delayed plasmodia, the second peak of synthesis may be turned on by a repeat of the commitment event.
在多头绒泡菌中,微管蛋白的合成受有丝分裂周期调控。实际上,所有微管蛋白的合成都局限于有丝分裂前紧挨着的2小时时间段内,微管蛋白合成的高峰伴随着微管蛋白mRNA水平的相应增加。微管蛋白mRNA积累开启和关闭的机制尚不清楚。为了探究微管蛋白调控与细胞周期控制之间的关系,我们利用热休克来延迟有丝分裂,并追踪了这些延迟期间微管蛋白的合成模式。热休克后观察到两个微管蛋白合成高峰。一个出现在没有热休克时本来会发生合成的时间,另一个高峰紧接在最终延迟的有丝分裂之前。这些结果显然是由于细胞周期调控的改变。在对照有丝分裂的时间,在延迟的原质团中未检测到有丝分裂活性,并且微管蛋白的行为显示与热休克蛋白的行为明显不同。我们认为,微管蛋白家族的蛋白质受一种热不稳定的有丝分裂控制机制调控,但一旦细胞开始一轮微管蛋白合成,“微管蛋白时钟”就独立于热敏感系统运行。在延迟的原质团中,第二个合成高峰可能是由启动事件的重复开启的。