Heintz N, Sive H L, Roeder R G
Mol Cell Biol. 1983 Apr;3(4):539-50. doi: 10.1128/mcb.3.4.539-550.1983.
We have analyzed the kinetics of accumulation of each of the individual core histone mRNAs throughout the HeLa cell cycle in cells synchronized by sequential thymidine and aphidicolin treatments. These analyses showed that during the S phase there was a 15-fold increase in the levels of histone mRNAs and that this resulted from both an increased rate of synthesis and a lengthening of the half-life of histone mRNAs. A comparison of the kinetics of accumulation of histone mRNA in the total cellular and nuclear RNA populations suggested an increased transcription rate through the S phase. Within 30 min after the inhibition of DNA synthesis in mid-S phase, the steady-state concentration and the rate of synthesis of histone mRNA each declined to their non-S-phase levels. Reactivation of histone mRNA accumulation could occur even after an extended mid-S-phase block in DNA synthesis. These results suggest that the mechanisms responsible for histone mRNA synthesis are not restricted to the G1/S boundary of the HeLa cell cycle, but can operate whenever DNA synthesis is occurring.
我们分析了经胸苷和阿非迪霉素顺序处理同步化的HeLa细胞在整个细胞周期中各个核心组蛋白mRNA的积累动力学。这些分析表明,在S期,组蛋白mRNA水平增加了15倍,这是由于合成速率增加和组蛋白mRNA半衰期延长所致。对总细胞和核RNA群体中组蛋白mRNA积累动力学的比较表明,整个S期转录速率增加。在S期中期DNA合成受到抑制后30分钟内,组蛋白mRNA的稳态浓度和合成速率均降至非S期水平。即使在S期中期DNA合成被长时间阻断后,组蛋白mRNA积累也可重新激活。这些结果表明,负责组蛋白mRNA合成的机制并不局限于HeLa细胞周期的G1/S边界,而是在DNA合成发生时均可起作用。