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在猿猴病毒40 DNA复制的体外系统中对喜树碱抗性人DNA拓扑异构酶I的特性研究。

Characterization of a camptothecin-resistant human DNA topoisomerase I in an in vitro system for Simian virus 40 DNA replication.

作者信息

Ishimi Y, Nishizawa M, Andoh T

机构信息

Mitsubishi Kasei Institute of Life Sciences, Tokyo, Japan.

出版信息

Eur J Biochem. 1991 Dec 18;202(3):835-9. doi: 10.1111/j.1432-1033.1991.tb16440.x.

Abstract

DNA topoisomerase I was required for bidirectional DNA replication in an in vitro system for Simian virus 40 (SV40) DNA replication with purified proteins in which the replication fork moved at the rate of 260 nucleotides/min on average. DNA topoisomerase I purified from camptothecin-resistant human lymphoblastoid cells, which confers high resistance of cellular DNA replication to camptothecin [Andoh, T., Ishii, K., Suzuki, Y., Ikegami, Y., Kusunoki, Y., Takemoto, Y. & Okada, K. (1987) Proc. Natl Acad. Sci. USA 84, 5565-5569], was characterized using this system. The activity of stimulating bidirectional DNA replication was comparable between two topoisomerase I from parental and resistant cells, i.e. in its dose-response relationship and in its time course for DNA synthesis. Camptothecin severely inhibited the leading as well as the lagging strand synthesis in the reaction containing the wild type topoisomerase I but not the mutant type topoisomerase I. The mutant type topoisomerase I was over 125-fold as resistant to camptothecin as the wild type topoisomerase I. These results are in good agreement with those on the sensitivity of cellular DNA synthesis to camptothecin in the resistant cells. These findings suggest that topoisomerase I is involved in cellular DNA replication as a swivelase and the mutation conferring camptothecin-resistance on the enzyme does not affect its functional efficiency in this system.

摘要

在一个用纯化蛋白进行猴病毒40(SV40)DNA复制的体外系统中,DNA拓扑异构酶I是双向DNA复制所必需的,在该系统中复制叉平均以每分钟260个核苷酸的速度移动。从喜树碱抗性人淋巴母细胞中纯化的DNA拓扑异构酶I赋予细胞DNA复制对喜树碱的高抗性[安藤,T.,石井,K.,铃木,Y.,池上,Y.,楠木,Y.,竹本,Y. & 冈田,K.(1987年)美国国家科学院院刊84,5565 - 5569],使用该系统对其进行了表征。来自亲代细胞和抗性细胞的两种拓扑异构酶I在刺激双向DNA复制的活性方面相当,即在其剂量反应关系和DNA合成的时间进程方面。喜树碱在含有野生型拓扑异构酶I的反应中严重抑制前导链和滞后链的合成,但不抑制突变型拓扑异构酶I。突变型拓扑异构酶I对喜树碱的抗性是野生型拓扑异构酶I的125倍以上。这些结果与抗性细胞中细胞DNA合成对喜树碱的敏感性结果非常一致。这些发现表明,拓扑异构酶I作为一种旋转酶参与细胞DNA复制,并且赋予该酶喜树碱抗性的突变不会影响其在该系统中的功能效率。

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