Fraser R S, Moreno F
J Cell Sci. 1976 Aug;21(3):497-521. doi: 10.1242/jcs.21.3.497.
The rates of polyadenylated messenger RNA and ribosomal RNA synthesis were measured in synchronously dividing cultures of fission yeast (Schizosaccharomyces pombe). Control asynchronous cultures, which had been exposed to the conditions used for preparing synchronous cultures, were investigated to check for effects of the synchronization procedure itself on RNA synthesis. After each period of DNA synthesis in synchronous culture, the rates of messenger and ribosomal RNA synthesis doubled, suggesting that gene number controls the rate of messenger and ribosomal RNA synthesis. This was confirmed by experiments with asynchronous, exponential-phase cultures in which DNA synthesis was inhibited by hydroxyurea. Both synchronous culture and hydroxyurea experiments suggested that there is a delay of 15 min (0-1 of the cell generation time) between replication of the DNA and transcription of both gene copies. A pattern of protein accumulation was calculated from changes in the rate of polyadenylated messenger RNA synthesis during synchronous culture. The simulated pattern indicates that protein is accumulated linearly, with a doubling in the rate of accumulation once per cell cycle. The simulated pattern of protein accumulation is very similar to measurements previously reported by other workers of changes in activities of 3 enzymes in synchronous cultures. It is suggested that the doubling of the rate of messenger RNA synthesis, as a consequence of the replication of the DNA once per cycle, provides the basis of a mechanism for control of the doubling of other cellular constituents during the cell cycle.
在裂殖酵母(粟酒裂殖酵母)同步分裂培养物中测定了多聚腺苷酸化信使核糖核酸和核糖体核糖核酸的合成速率。对已暴露于用于制备同步培养物的条件下的对照异步培养物进行了研究,以检查同步化程序本身对核糖核酸合成的影响。在同步培养物的每个DNA合成期之后,信使核糖核酸和核糖体核糖核酸的合成速率加倍,这表明基因数量控制着信使核糖核酸和核糖体核糖核酸的合成速率。用羟基脲抑制DNA合成的异步指数生长期培养物的实验证实了这一点。同步培养和羟基脲实验均表明,在DNA复制与两个基因拷贝的转录之间存在15分钟的延迟(细胞世代时间的0-1)。根据同步培养期间多聚腺苷酸化信使核糖核酸合成速率的变化计算出了蛋白质积累模式。模拟模式表明蛋白质呈线性积累,每个细胞周期积累速率加倍一次。模拟的蛋白质积累模式与其他研究人员先前报道的同步培养物中3种酶活性变化的测量结果非常相似。有人提出,由于每个周期DNA复制导致信使核糖核酸合成速率加倍,为细胞周期中其他细胞成分加倍的控制机制提供了基础。