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拓扑异构酶I在单链DNA断裂转化为双链DNA断裂过程中的作用。

Contribution of topoisomerase I to conversion of single-strand into double-strand DNA breaks.

作者信息

Kowalska-Loth B, Bubko I, Komorowska B, Szumiel I, Staron K

机构信息

Institute of Biochemistry, Warsaw University, Poland.

出版信息

Mol Biol Rep. 1998 Jan;25(1):21-6. doi: 10.1023/a:1006831527609.

Abstract

An in vitro system composed of nicked pBR322 DNA and purified topoisomerase I was employed to study the efficiency of the topoisomerase I-driven single-strand to double-strand DNA breaks conversion. At 1.4 x 10(5) topoisomerase I activity units per mg DNA about 20% single-strand nicks were converted into double-strand breaks during 30 min due to topoisomerase I action. Camptothecin inhibited the conversion. The conversion was also inhibited when the relaxing activity of the used topoisomerase I was increased by phosphorylation of the enzyme with casein kinase 2. The presented data suggest that topoisomerase I may be involved in production of double-stranded breaks in irradiated cells and that this process positively depends on the amount of topoisomerase I but not on its phosphorylation state.

摘要

采用由切口的pBR322 DNA和纯化的拓扑异构酶I组成的体外系统,研究拓扑异构酶I驱动的单链到双链DNA断裂转化的效率。在每毫克DNA 1.4×10⁵拓扑异构酶I活性单位的条件下,由于拓扑异构酶I的作用,在30分钟内约20%的单链切口转化为双链断裂。喜树碱抑制这种转化。当用酪蛋白激酶2对所用的拓扑异构酶I进行磷酸化处理以提高其松弛活性时,这种转化也受到抑制。所呈现的数据表明,拓扑异构酶I可能参与受辐照细胞中双链断裂的产生,并且这一过程确实依赖于拓扑异构酶I的量,而不依赖于其磷酸化状态。

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