Riddle V G, Pardee A B
J Cell Physiol. 1980 Apr;103(1):11-5. doi: 10.1002/jcp.1041030103.
Major proteins synthesized by Swiss 3T3 cells at different stages of the cell cycle have been analyzed using double isotope labeling and one-dimensional SDS-polyacrylamide slab gels. The synthesis of actin was previously shown to be markedly enhanced a few hours after quiescent cells initiated growth following addition of serum. In contrast, the synthesis of actin remained at a constant rate, similar to that in quiescent cells, relative to synthesis of other proteins during the entire cell cycle. We conclude that enhanced actin synthesis is a process specific for the G0 to S transit, and may serve as a marker event during this interval. In contrast, three other proteins (90,000, 57,000, and 33,000 daltons) were synthesized throughout the cell cycle at higher rates than in G0 cells, and thus, are markers characteristic of cells traversing the cell cycle. A transient increase, such as seen for actin synthesis, by cells emerging from quiescence, may represent a process that these cells must perform before they can enter the G1 portion of the cell cycle. A transient event such as this need not be a periodic event that occurs during each cycle.
利用双同位素标记和一维SDS-聚丙烯酰胺平板凝胶,对瑞士3T3细胞在细胞周期不同阶段合成的主要蛋白质进行了分析。先前研究表明,在添加血清后,静止细胞开始生长的几个小时内,肌动蛋白的合成显著增强。相比之下,在整个细胞周期中,相对于其他蛋白质的合成,肌动蛋白的合成速率保持恒定,与静止细胞中的合成速率相似。我们得出结论,肌动蛋白合成增强是从G0期到S期转变过程中的一个特定过程,并且可能是该时间段内的一个标志性事件。相比之下,另外三种蛋白质(90000、57000和33000道尔顿)在整个细胞周期中的合成速率都高于G0期细胞,因此是细胞穿越细胞周期的特征性标志物。从静止状态出现的细胞中观察到的肌动蛋白合成那样的短暂增加,可能代表这些细胞在进入细胞周期的G1期之前必须执行的一个过程。这样的短暂事件不一定是每个周期都会发生的周期性事件。