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DNA拓扑异构酶II在中国仓鼠卵巢细胞有丝分裂染色体形成中是必需的:使用抑制剂4'-去甲基表鬼臼毒素9-(4,6-O-亚噻吩基-β-D-吡喃葡萄糖苷)的研究

DNA topoisomerase II is required for formation of mitotic chromosomes in Chinese hamster ovary cells: studies using the inhibitor 4'-demethylepipodophyllotoxin 9-(4,6-O-thenylidene-beta-D-glucopyranoside).

作者信息

Charron M, Hancock R

机构信息

Centre de Recherche en Cancérologie, l'Université Laval, Hôtel-Dieu Hospital, Québec, Canada.

出版信息

Biochemistry. 1990 Oct 16;29(41):9531-7. doi: 10.1021/bi00493a006.

DOI:10.1021/bi00493a006
PMID:2176848
Abstract

To study the biochemical processes which DNA topoisomerase II carries out in mammalian cells, which have not been identified, we have examined the effects on chromosome replication in Chinese hamster ovary cells of an agent which traps molecules of topoisomerase II when they are covalently integrated into DNA during their reaction. This agent, 4'-demethylepipodophyllotoxin 9-(4,6-O-thenylidene-beta-D-glucopyranoside) (VM-26), targets this enzyme specifically according to a compelling body of evidence. Using synchronously growing cells, we found that VM-26 at a cytotoxic concentration (0.08 microM) did not affect DNA replication during the S phase. The formation of mitotic chromosomes was delayed by 4 h, and its rate was reduced thereafter, causing a delay in mitosis of greater than 14 h in 65% of the cells; in some cells, the chromatin was aberrantly condensed, forming diffuse chromosomes or particles. Chromosome formation was completely inhibited at 0.32 microM VM-26. DNA fragments derived from topoisomerase II molecules covalently integrated in DNA and trapped by VM-26 were detected by FIGE analysis in the G2 period, but not during the S phase. The delay of chromosome formation appeared to be caused by two factors: first, a delay in the completion of DNA replication, because progress of some cells to mitosis after removal of VM-26 was prevented by aphidicolin, an inhibitor of DNA polymerases alpha and delta; and second, a delay of chromosome formation in cells which had apparently completed DNA replication. The observations reported here show that topoisomerase II carries out reactions which are essential for formation of mitotic chromosomes.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

为了研究尚未明确的DNA拓扑异构酶II在哺乳动物细胞中所执行的生化过程,我们检测了一种试剂对中国仓鼠卵巢细胞染色体复制的影响。当拓扑异构酶II分子在反应过程中与DNA共价结合时,该试剂能将其捕获。大量确凿证据表明,这种试剂4'-去甲基表鬼臼毒素9-(4,6-O-亚苄基-β-D-吡喃葡萄糖苷)(VM-26)能特异性作用于该酶。利用同步生长的细胞,我们发现细胞毒性浓度(0.08 microM)的VM-26在S期并不影响DNA复制。有丝分裂染色体的形成延迟了4小时,之后其形成速率降低,导致65%的细胞有丝分裂延迟超过14小时;在一些细胞中,染色质异常浓缩,形成弥散的染色体或颗粒。在0.32 microM VM-26时,染色体形成被完全抑制。通过FIGE分析在G2期检测到了源自与DNA共价结合并被VM-26捕获的拓扑异构酶II分子的DNA片段,但在S期未检测到。染色体形成的延迟似乎由两个因素导致:第一,DNA复制完成延迟,因为去除VM-26后,一些细胞进入有丝分裂的进程被DNA聚合酶α和δ的抑制剂阿非科林所阻止;第二,在显然已完成DNA复制的细胞中,染色体形成延迟。此处报道的观察结果表明,拓扑异构酶II执行着对有丝分裂染色体形成至关重要的反应。(摘要截短至250字)

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1
DNA topoisomerase II is required for formation of mitotic chromosomes in Chinese hamster ovary cells: studies using the inhibitor 4'-demethylepipodophyllotoxin 9-(4,6-O-thenylidene-beta-D-glucopyranoside).DNA拓扑异构酶II在中国仓鼠卵巢细胞有丝分裂染色体形成中是必需的:使用抑制剂4'-去甲基表鬼臼毒素9-(4,6-O-亚噻吩基-β-D-吡喃葡萄糖苷)的研究
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Arrest of replication fork progression at sites of topoisomerase II-mediated DNA cleavage in human leukemia CEM cells incubated with VM-26.在与VM-26孵育的人白血病CEM细胞中,拓扑异构酶II介导的DNA切割位点处复制叉进展的停滞。
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Teniposide-resistant CEM cells, which express mutant DNA topoisomerase II alpha, when treated with non-complex-stabilizing inhibitors of the enzyme, display no cross-resistance and reveal aberrant functions of the mutant enzyme.表达突变型DNA拓扑异构酶IIα的替尼泊苷耐药CEM细胞,在用该酶的非复合物稳定抑制剂处理时,未显示交叉耐药性,并揭示了突变酶的异常功能。
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引用本文的文献

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A mitotic topoisomerase II checkpoint in budding yeast is required for genome stability but acts independently of Pds1/securin.芽殖酵母中的有丝分裂拓扑异构酶II检查点对于基因组稳定性是必需的,但它独立于Pds1/分离酶发挥作用。
Genes Dev. 2006 May 1;20(9):1162-74. doi: 10.1101/gad.1367206.
2
In vivo etoposide-resistant C6 glioma cell line: significance of altered DNA topoisomerase II activity in multi-drug resistance.体内依托泊苷耐药C6胶质瘤细胞系:DNA拓扑异构酶II活性改变在多药耐药中的意义
J Neurooncol. 1998 Jan;36(1):41-53. doi: 10.1023/a:1005718912236.
3
Immunohistochemical detection of DNA topoisomerase I in formalin fixed, paraffin wax embedded normal tissues and in ovarian carcinomas.
福尔马林固定、石蜡包埋的正常组织及卵巢癌组织中DNA拓扑异构酶I的免疫组织化学检测
Mol Pathol. 1997 Oct;50(5):247-53. doi: 10.1136/mp.50.5.247.
4
Chromosomes with two intact axial cores are induced by G2 checkpoint override: evidence that DNA decatenation is not required to template the chromosome structure.通过G2检查点超控诱导出具有两个完整轴向核心的染色体:证明DNA解连环对于染色体结构模板化并非必需。
J Cell Biol. 1997 Jan 13;136(1):29-43. doi: 10.1083/jcb.136.1.29.
5
Structure and conformational changes of DNA topoisomerase II visualized by electron microscopy.通过电子显微镜观察DNA拓扑异构酶II的结构和构象变化
Proc Natl Acad Sci U S A. 1996 Jun 11;93(12):5936-40. doi: 10.1073/pnas.93.12.5936.
6
Chromosome recombination and defective genome segregation induced in Chinese hamster cells by the topoisomerase II inhibitor VM-26.
Chromosoma. 1991 Feb;100(2):97-102. doi: 10.1007/BF00418242.
7
Cell cycle control of higher-order chromatin assembly around naked DNA in vitro.体外裸DNA周围高阶染色质组装的细胞周期控制
J Cell Biol. 1991 Dec;115(6):1479-89. doi: 10.1083/jcb.115.6.1479.
8
Inhibitors of DNA topoisomerase II prevent chromatid separation in mammalian cells but do not prevent exit from mitosis.
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9
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