Bravo R, Celis J E
J Cell Biol. 1980 Mar;84(3):795-802. doi: 10.1083/jcb.84.3.795.
The polypeptides synthesized during the cell cycle of HeLa cells were analyzed by means of two-dimensional gel electrophoresis followed by fluorography under conditions in which the position of 700 polypeptides (acidic and basic) could be reproducibly assessed. Mitotic cells obtained by mechanical detachment and synchronized cells in other stages of the cell cycle were labeled with [35S]methionine for 30-min pulses or for long terms starting at the beginning of each phase. Visual comparison of the polypeptide maps obtained in the different stages of the cell cycle showed that these were strikingly similar, and there was no indication that the synthesis of any of the detected polypeptides was confined to only one of the cell cycle phases. Quantitation of 99 abundant polypeptides (acidic and basic) in pulse-labeled and long-term labeled cells revealed that the relative amount (i.e., the rate of synthesis) of most polypeptides, including total actin, alpha-actinin, 6 abundant basic nonhistone proteins, and 13 major acidic proteins present in Triton cytoskeletons, remains constant throughout the cell cycle. Among the few variable polypeptides (markers), we have identified alpha- and beta-tubulin (increase in M), the subunit of the 100-A filament protein "fibroblast type" (decreases in M), and a 36,000 mol wt acidic cytoarchitectural protein that increases in S. A few other unidentified polypeptides have also been found to vary in M and in M and G2, but no marker was found in G1.
通过二维凝胶电泳,随后在可重复评估700种多肽(酸性和碱性)位置的条件下进行荧光自显影,分析了海拉细胞(HeLa cells)细胞周期中合成的多肽。通过机械分离获得的有丝分裂细胞以及处于细胞周期其他阶段的同步化细胞,用[35S]甲硫氨酸进行30分钟脉冲标记或从每个阶段开始时进行长期标记。对在细胞周期不同阶段获得的多肽图谱进行视觉比较,结果表明它们非常相似,没有迹象表明任何检测到的多肽的合成仅限于细胞周期的某一个阶段。对脉冲标记和长期标记细胞中的99种丰富多肽(酸性和碱性)进行定量分析,结果显示,大多数多肽的相对含量(即合成速率),包括总肌动蛋白、α-辅肌动蛋白、6种丰富的碱性非组蛋白以及存在于Triton细胞骨架中的13种主要酸性蛋白,在整个细胞周期中保持恒定。在少数可变多肽(标记物)中,我们鉴定出α-和β-微管蛋白(在M期增加)、100 Å细丝蛋白“成纤维细胞型”的亚基(在M期减少)以及一种分子量为36,000的酸性细胞结构蛋白,其在S期增加。还发现一些其他未鉴定的多肽在M期以及M期和G2期有所变化,但在G1期未发现标记物。