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用蛋白质合成抑制剂处理的海拉细胞核中的DNA复制系统。

A system of DNA replication in HeLa nuclei treated with inhibitors of protein synthesis.

作者信息

Nagata K, Enomoto T, Yamada M A

出版信息

Biochim Biophys Acta. 1981 May 29;653(3):316-30. doi: 10.1016/0005-2787(81)90188-x.

Abstract

An in vitro DNA synthesizing system consisting os isolated nuclei from HeLa cells which had been treated with inhibitors of protein synthesis was investigated. Treatment with both 30 microgram/ml cycloheximide and 10 microgram/ml puromycin of S-phase cells reduced the rate of DNA synthesis immediately; however, the overall DNA synthesis continued for up to 4 h with a diminished rate and then ceased. In the nuclei which were isolated from the cells which had been incubated with these drugs for 6 h, little incorporation of [3H]TTP into acid-insoluble materials was observed. Addition of cytosol prepared from cells actively synthesizing DNA induced the incorporation of [3H]TTP in these nuclei, while little induction was observed by the addition of cytosol prepared from drug-treated cells in spite of the fact that the latter cytosol stimulated DNA synthesis in isolated nuclei from non-treated cells. The induced DNA synthesis was shown to require Mg2+, all four deoxyribonucleoside triphosphates and ATP, and to proceed discontinuously. The activity inducing DNA synthesis in drug-treated nuclei fluctuated with the phases in a cell cycle and it was not ascribed solely to DNA polymerase alpha nor to DNA ligase.

摘要

对一个体外DNA合成系统进行了研究,该系统由用蛋白质合成抑制剂处理过的HeLa细胞的分离细胞核组成。用30微克/毫升环己酰亚胺和10微克/毫升嘌呤霉素处理S期细胞,会立即降低DNA合成速率;然而,总的DNA合成会以降低的速率持续长达4小时,然后停止。在从用这些药物孵育6小时的细胞中分离出的细胞核中,几乎观察不到[3H]TTP掺入酸不溶性物质中。添加从活跃合成DNA的细胞制备的胞质溶胶会诱导这些细胞核中[3H]TTP的掺入,而添加从药物处理细胞制备的胞质溶胶几乎观察不到诱导作用,尽管后者的胞质溶胶能刺激未处理细胞分离细胞核中的DNA合成。诱导的DNA合成显示需要Mg2+、所有四种脱氧核糖核苷三磷酸和ATP,并且是不连续进行的。药物处理细胞核中诱导DNA合成的活性随细胞周期的阶段而波动,并且它不仅仅归因于DNA聚合酶α或DNA连接酶。

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