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喜树碱对小牛胸腺拓扑异构酶I介导的DNA切割/连接反应的影响:喜树碱抑制DNA连接的证据。喜树碱对拓扑异构酶I介导的DNA连接的抑制作用。

Effect of CPT on the DNA cleavage/religation reaction mediated by calf thymus Topoisomerase I: evidence of an inhibition of DNA religation. Inhibition of Topoisomerase I-mediated DNA religation by CPT.

作者信息

Carboni M C, Coderoni S

机构信息

Department of Molecular, Cellular and Animal Biology, University of Camerino, Italy.

出版信息

Mol Biol Rep. 1994;20(3):129-33. doi: 10.1007/BF00990544.

DOI:10.1007/BF00990544
PMID:7565652
Abstract

The uncoupling of the calf thymus Topoisomerase I-mediated forward DNA cleavage reaction from the religation event by a rapid shift of cleavage temperature either from 37 degrees C to 0 degrees C or from 37 degrees C to 56 degrees C has been studied and utilized to elucidate the molecular mechanism by which camptothecin, a clinically relevant antineoplastic agent, influences the half reactions of the enzyme. Results of heating and cooling religation-inducing treatments have been compared: both temperature extremes reduce the amount of protein-linked DNA breaks to background levels, thereby affecting cleavage reversal. Camptothecin is found to stabilize the enzyme-DNA intermediate, by inhibition of the Topoisomerase I-mediated rejoining of cleaved DNA, even when the drug is added after formation of the complex. We conclude that: 1. Heating and cooling treatments show a pronounced effect on the DNA cleavage-religation equilibrium. The efficacy of cold is more pronounced than that of heat. 2. Reversal of the enzyme-DNA intermediate favors the DNA resealing versus the closed relaxed form. 3. Camptothecin affects the heat or cold induced religation: in fact in both cases the drug delays the religation step.

摘要

通过将切割温度从37℃快速转移至0℃或从37℃快速转移至56℃,使小牛胸腺拓扑异构酶I介导的正向DNA切割反应与重新连接事件解偶联,已对其进行了研究,并用于阐明喜树碱(一种临床相关的抗肿瘤药物)影响该酶半反应的分子机制。已比较了加热和冷却重新连接诱导处理的结果:两个极端温度均将蛋白质连接的DNA断裂量降低至背景水平,从而影响切割逆转。发现喜树碱可通过抑制拓扑异构酶I介导的切割DNA重新连接来稳定酶-DNA中间体,即使在复合物形成后添加该药物也是如此。我们得出以下结论:1.加热和冷却处理对DNA切割-重新连接平衡有显著影响。冷处理的效果比热处理更显著。2.酶-DNA中间体的逆转有利于DNA重新封闭而非闭环松弛形式。3.喜树碱影响热或冷诱导的重新连接:实际上在两种情况下,该药物都会延迟重新连接步骤。

相似文献

1
Effect of CPT on the DNA cleavage/religation reaction mediated by calf thymus Topoisomerase I: evidence of an inhibition of DNA religation. Inhibition of Topoisomerase I-mediated DNA religation by CPT.喜树碱对小牛胸腺拓扑异构酶I介导的DNA切割/连接反应的影响:喜树碱抑制DNA连接的证据。喜树碱对拓扑异构酶I介导的DNA连接的抑制作用。
Mol Biol Rep. 1994;20(3):129-33. doi: 10.1007/BF00990544.
2
Effect of CPT on the calf thymus Topoisomerase I-mediated DNA breakage-reunion reaction: optimal conditions for the formation and reversal of the CPT trapped Topoisomerase I cleavable complex.喜树碱对小牛胸腺拓扑异构酶I介导的DNA断裂-重连反应的影响:喜树碱捕获的拓扑异构酶I可裂解复合物形成与逆转的最佳条件。
Mol Biol Rep. 1993 Feb;17(2):129-34. doi: 10.1007/BF00996220.
3
New technique for uncoupling the cleavage and religation reactions of eukaryotic topoisomerase I. The mode of action of camptothecin at a specific recognition site.真核生物拓扑异构酶I切割与重新连接反应解偶联的新技术。喜树碱在特定识别位点的作用模式。
J Mol Biol. 1991 Dec 5;222(3):669-78. doi: 10.1016/0022-2836(91)90503-x.
4
Differential induction of Leishmania donovani bi-subunit topoisomerase I-DNA cleavage complex by selected flavones and camptothecin: activity of flavones against camptothecin-resistant topoisomerase I.选定黄酮类化合物和喜树碱对杜氏利什曼原虫双亚基拓扑异构酶I-DNA切割复合物的差异诱导作用:黄酮类化合物对喜树碱抗性拓扑异构酶I的活性
Nucleic Acids Res. 2006 Feb 18;34(4):1121-32. doi: 10.1093/nar/gkj502. Print 2006.
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ATP modulates poly(ADP-ribose) polymerase-1-facilitated topoisomerase I-linked DNA religation in the presence of camptothecin.在喜树碱存在的情况下,ATP调节聚(ADP - 核糖)聚合酶-1促进的拓扑异构酶I连接的DNA重新连接。
Mol Pharmacol. 2008 Jun;73(6):1829-37. doi: 10.1124/mol.107.044438. Epub 2008 Mar 18.
6
Camptothecin inhibits both the cleavage and religation reactions of eukaryotic DNA topoisomerase I.
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7
Mode of action of topoisomerase II-targeting agents at a specific DNA sequence. Uncoupling the DNA binding, cleavage and religation events.靶向拓扑异构酶II的药物在特定DNA序列处的作用模式。使DNA结合、切割和重新连接事件解偶联。
J Mol Biol. 1992 Dec 5;228(3):778-86. doi: 10.1016/0022-2836(92)90863-f.
8
Camptothecin induces protein-linked DNA breaks via mammalian DNA topoisomerase I.喜树碱通过哺乳动物DNA拓扑异构酶I诱导蛋白质连接的DNA断裂。
J Biol Chem. 1985 Nov 25;260(27):14873-8.
9
DNA recombinase activity of eukaryotic DNA topoisomerase I; effects of camptothecin and other inhibitors.真核生物DNA拓扑异构酶I的DNA重组酶活性;喜树碱及其他抑制剂的作用
Mutat Res. 1995 Sep;337(2):135-45. doi: 10.1016/0921-8777(95)00019-g.
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Induction of cleavage in topoisomerase I c-DNA by topoisomerase I enzymes from calf thymus and wheat germ in the presence and absence of camptothecin.在有和没有喜树碱的情况下,小牛胸腺和小麦胚芽中的拓扑异构酶I酶对拓扑异构酶I cDNA切割的诱导作用。
Nucleic Acids Res. 1993 Nov 11;21(22):5157-66. doi: 10.1093/nar/21.22.5157.

本文引用的文献

1
Effect of CPT on the calf thymus Topoisomerase I-mediated DNA breakage-reunion reaction: optimal conditions for the formation and reversal of the CPT trapped Topoisomerase I cleavable complex.喜树碱对小牛胸腺拓扑异构酶I介导的DNA断裂-重连反应的影响:喜树碱捕获的拓扑异构酶I可裂解复合物形成与逆转的最佳条件。
Mol Biol Rep. 1993 Feb;17(2):129-34. doi: 10.1007/BF00996220.
2
Induction of topoisomerase I-mediated DNA cleavage by a new indolocarbazole, ED-110.新型吲哚咔唑ED-110诱导拓扑异构酶I介导的DNA切割
Cancer Res. 1993 Feb 1;53(3):490-4.
3
Camptothecin induces protein-linked DNA breaks via mammalian DNA topoisomerase I.
喜树碱通过哺乳动物DNA拓扑异构酶I诱导蛋白质连接的DNA断裂。
J Biol Chem. 1985 Nov 25;260(27):14873-8.
4
DNA topoisomerases.DNA拓扑异构酶
Annu Rev Biochem. 1985;54:665-97. doi: 10.1146/annurev.bi.54.070185.003313.
5
Sequence-dependent effect of camptothecin on human topoisomerase I DNA cleavage.喜树碱对人拓扑异构酶I DNA切割的序列依赖性效应
J Mol Biol. 1988 Jul 20;202(2):333-42. doi: 10.1016/0022-2836(88)90462-7.
6
Identification of mammalian DNA topoisomerase I as an intracellular target of the anticancer drug camptothecin.鉴定哺乳动物DNA拓扑异构酶I为抗癌药物喜树碱的细胞内靶点。
Cancer Res. 1988 Apr 1;48(7):1722-6.
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Topoisomerase-targeting antitumor drugs.
Biochim Biophys Acta. 1989 Dec 17;989(2):163-77. doi: 10.1016/0304-419x(89)90041-3.
8
The basis for camptothecin enhancement of DNA breakage by eukaryotic topoisomerase I.喜树碱增强真核生物拓扑异构酶I导致DNA断裂的作用基础。
Nucleic Acids Res. 1989 Nov 11;17(21):8521-32. doi: 10.1093/nar/17.21.8521.
9
DNA topoisomerase poisons as antitumor drugs.作为抗肿瘤药物的DNA拓扑异构酶毒物
Annu Rev Biochem. 1989;58:351-75. doi: 10.1146/annurev.bi.58.070189.002031.
10
On the mechanism of topoisomerase I inhibition by camptothecin: evidence for binding to an enzyme-DNA complex.关于喜树碱抑制拓扑异构酶I的机制:与酶-DNA复合物结合的证据。
Biochemistry. 1989 May 30;28(11):4629-38. doi: 10.1021/bi00437a018.