Storms R K, Ord R W, Greenwood M T, Mirdamadi B, Chu F K, Belfort M
Mol Cell Biol. 1984 Dec;4(12):2858-64. doi: 10.1128/mcb.4.12.2858-2864.1984.
Synchronous populations of Saccharomyces cerevisiae cells, generated by two independent methods, have been used to show that thymidylate synthase, in contrast to the vast majority of cellular proteins thus far examined, fluctuates periodically during the S. cerevisiae cell cycle. The enzyme, as assayed by two different methods, accumulated during S period and peaked in mid to late S phase, and then its level dropped. These observations suggest that both periodic synthesis and the instability of the enzyme contribute to the activity profile seen during the cell cycle. Accumulation of thymidylate synthase is determined at the level of its transcript, with synthase-specific mRNA levels increasing at least 10-fold to peak near the beginning of S period and then falling dramatically to basal levels after the onset of DNA synthesis. This mRNA peak coincided with the time during the cell cycle when thymidylate synthase levels were increasing maximally and immediately preceded the peak of DNA synthesis, for which the enzyme provides precursor dTMP.
通过两种独立方法产生的酿酒酵母细胞同步群体已被用于表明,与迄今为止检测的绝大多数细胞蛋白不同,胸苷酸合成酶在酿酒酵母细胞周期中呈周期性波动。通过两种不同方法测定,该酶在S期积累,并在S期中后期达到峰值,然后其水平下降。这些观察结果表明,酶的周期性合成和不稳定性都导致了细胞周期中观察到的活性谱。胸苷酸合成酶的积累在其转录水平上被确定,合酶特异性mRNA水平至少增加10倍,在S期开始时达到峰值,然后在DNA合成开始后急剧下降到基础水平。这个mRNA峰值与细胞周期中胸苷酸合成酶水平最大程度增加的时间一致,并且紧接在DNA合成峰值之前,该酶为DNA合成提供前体dTMP。