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热同步化的四膜虫DNA复制时间表分析

Analysis of the schedule of DNA replication in heat-synchronized Tetrahymena.

作者信息

Jeffery W R, Frankel J, DeBault L E, Jenkins L M

出版信息

J Cell Biol. 1973 Oct;59(1):1-11. doi: 10.1083/jcb.59.1.1.

Abstract

The temporal schedule of DNA replication in heat-synchronized Tetrahymena was studied by autoradiographic and cytofluorometric methods. It was shown that some cells, which were synchronized by selection of individual dividing cells or by temporary thymidine starvation, incorporated [(3)H]thymidine into macronuclei in a periodic fashion during the heat-shock treatment. It was concluded that supernumerary S periods occurred while cell division was blocked by high temperature. The proportion of cells which initiated supernumerary S periods was found to be dependent on the duration of the heat-shock treatment and on the cell cycle stage when the first heat shock was applied. Cytofluorometric measurements of Feulgen-stained macronuclei during the heat-shock treatment indicated that the DNA complement of these cells was substantially increased and probably duplicated during the course of each S period. Estimates of DNA content also suggested that the rate of DNA synthesis progressively declined during long heat-shock treatments. These results indicate that the mechanism which brings about heat-induced division synchrony is not an interruption of the process of DNA replication. Further experiments were concerned with the regulation of DNA synthesis during the first synchronized division cycle. It was shown that participation in DNA synthesis at this time increased as more cells were able to conclude the terminal S period during the preceding heat-shock treatment. It is suggested that a discrete period of time is necessary after the completion of DNA synthesis before another round of DNA synthesis can be initiated.

摘要

采用放射自显影和细胞荧光测定法研究了热同步处理的四膜虫DNA复制的时间进程。结果表明,一些通过挑选单个分裂细胞或短暂胸腺嘧啶核苷饥饿实现同步化的细胞,在热休克处理期间以周期性方式将[³H]胸腺嘧啶核苷掺入大核中。得出的结论是,在细胞分裂被高温阻断时会出现额外的S期。发现启动额外S期的细胞比例取决于热休克处理的持续时间以及首次热休克施加时的细胞周期阶段。热休克处理期间对Feulgen染色大核的细胞荧光测定表明,这些细胞的DNA含量大幅增加,并且可能在每个S期过程中发生了复制。DNA含量的估计还表明,在长时间热休克处理期间DNA合成速率逐渐下降。这些结果表明,导致热诱导分裂同步化的机制不是DNA复制过程的中断。进一步的实验关注第一个同步分裂周期中DNA合成的调控。结果表明,随着更多细胞能够在前一次热休克处理期间完成末期S期,此时参与DNA合成的细胞增多。有人提出,在DNA合成完成后,需要一段离散的时间才能启动新一轮的DNA合成。

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