首页> 外文期刊>Molecular and Cellular Biology >Regulation of human histone gene expression: kinetics of accumulation and changes in the rate of synthesis and in the half-lives of individual histone mRNAs during the HeLa cell cycle.
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Regulation of human histone gene expression: kinetics of accumulation and changes in the rate of synthesis and in the half-lives of individual histone mRNAs during the HeLa cell cycle.

机译:人组蛋白基因表达的调节:在HeLa细胞周期中的累积动力学和合成率的变化以及单个组蛋白MRNA的半衰期。

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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.
机译:我们已经分析了通过顺序胸苷和蚜虫蛋白处理同步的细胞中的每种单个核心组蛋白mRNA的累积动力学。这些分析表明,在S阶段期间,组蛋白MRNA的水平增加了15倍,并且这是由于合成率增加和组蛋白MRNA的半衰期增加。在总细胞和核RNA群中,组蛋白mRNA积累动力学的比较表明通过S期增加了转录率。在MID-S期抑制DNA合成后30分钟内,稳态浓度和组蛋白mRNA的合成速率下降到其非S相水平。即使在DNA合成中的延长的中间S相块之后,也可以发生组蛋白mRNA积累的再活化。这些结果表明,负责组蛋白mRNA合成的机制不限于HeLa细胞周期的G1 / s边界,但可以每当发生DNA合成时运行。

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