• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Chromosome recombination and defective genome segregation induced in Chinese hamster cells by the topoisomerase II inhibitor VM-26.

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

Chromosoma. 1991 Feb;100(2):97-102. doi: 10.1007/BF00418242.

DOI:10.1007/BF00418242
PMID:1849068
Abstract

We found that 4'-demethylepipodophyllotoxinthenylidene-beta-D-glucoside (VM-26; Teniposide), which specifically inhibits the enzyme DNA topoisomerase II, induces the formation of quadriradial chromosomes in Chinese hamster ovary cells. VM-26 traps topoisomerase II molecules when they are covalently integrated into DNA during their reaction. Quadriradial chromosomes are formed by reciprocal exchange of double-stranded DNA between single chromatids of two different chromosomes. Using synchronised cells, we found that they were formed after a single replication cycle in the presence of VM-26 at a low concentration (0.008 micro M), which does not affect DNA replication, and occurred in 50% of the mitotic cells at a concentration of 0.16 micro M. They were also formed when VM-26 was present for only 1.5 h before mitosis, after the completion of S-phase DNA replication. Chromatids bearing a translocated segment of another chromatid, which were derived from recombined chromosomes, were observed in late metaphase cells. Segregation of the daughter genomes was defective in many mitotic cells, probably because chromatids with two or no centromeres and kinetochores, formed from chromosomes recombined between their centromeres, could not be segregated. In the light of evidence that topoisomerase II molecules covalently integrated in DNA are trapped and therefore more abundant in the presence of VM-26, and that this enzyme can effect recombination of double-stranded DNA in vitro, we interpret these observations as evidence that topoisomerase II can mediate chromosome recombination in vivo.

摘要

相似文献

1
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.
2
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
Biochemistry. 1990 Oct 16;29(41):9531-7. doi: 10.1021/bi00493a006.
3
The topoisomerase II inhibitor VM-26 induces marked changes in histone H1 kinase activity, histones H1 and H3 phosphorylation, and chromosome condensation in G2 phase and mitotic BHK cells.拓扑异构酶II抑制剂VM-26可诱导处于G2期和有丝分裂期的BHK细胞的组蛋白H1激酶活性、组蛋白H1和H3磷酸化以及染色体凝聚发生显著变化。
J Cell Biol. 1990 Nov;111(5 Pt 1):1753-62. doi: 10.1083/jcb.111.5.1753.
4
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。
Cancer Res. 1993 Dec 15;53(24):5946-53.
5
Teniposide, a topoisomerase II inhibitor, prevents chromosome condensation and separation but not decondensation in fertilized surf clam (Spisula solidissima) oocytes.替尼泊苷是一种拓扑异构酶II抑制剂,它能阻止受精的 surf 蛤(Spisula solidissima)卵母细胞中的染色体浓缩和分离,但不能阻止其解聚。
Dev Biol. 1990 Nov;142(1):224-32. doi: 10.1016/0012-1606(90)90166-g.
6
Differences in inhibition of chromosome separation and G2 arrest by DNA topoisomerase II inhibitors merbarone and VM-26.DNA拓扑异构酶II抑制剂美巴龙和VM-26在抑制染色体分离和G2期阻滞方面的差异。
Cancer Res. 1995 Apr 1;55(7):1509-16.
7
Inhibition of DNA topoisomerase II by ICRF-193 induces polyploidization by uncoupling chromosome dynamics from other cell cycle events.ICRF-193对DNA拓扑异构酶II的抑制作用通过使染色体动态变化与其他细胞周期事件解偶联而诱导多倍体化。
J Cell Biol. 1994 Sep;126(6):1341-51. doi: 10.1083/jcb.126.6.1341.
8
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.
9
Integration of simian virus 40 into cellular DNA occurs at or near topoisomerase II cleavage hot spots induced by VM-26 (teniposide).猿猴病毒40整合进细胞DNA发生在由VM-26(替尼泊苷)诱导的拓扑异构酶II切割热点处或其附近。
Mol Cell Biol. 1993 Oct;13(10):6190-200. doi: 10.1128/mcb.13.10.6190-6200.1993.
10
Effects of an inhibitor of topoisomerase II, ICRF-193 on the formation of ultraviolet-induced chromosomal aberrations.拓扑异构酶II抑制剂ICRF-193对紫外线诱导的染色体畸变形成的影响。
Mutat Res. 1998 Aug 3;404(1-2):35-8. doi: 10.1016/s0027-5107(98)00092-x.

引用本文的文献

1
Topoisomerase II alpha inhibition can overcome taxane-resistant prostate cancer through DNA repair pathways.拓扑异构酶 IIα 抑制作用可通过 DNA 修复途径克服紫杉烷类耐药性前列腺癌。
Sci Rep. 2021 Nov 15;11(1):22284. doi: 10.1038/s41598-021-01697-2.
2
Common chromatin structures at breakpoint cluster regions may lead to chromosomal translocations found in chronic and acute leukemias.断点簇集区域常见的染色质结构可能导致在慢性和急性白血病中发现的染色体易位。
Hum Genet. 2006 Jun;119(5):479-95. doi: 10.1007/s00439-006-0146-9. Epub 2006 Mar 30.
3
Inhibition of DNA topoisomerase II in living cells stimulates illegitimate recombination.

本文引用的文献

1
CYTOLOGICAL EVIDENCE FOR CROSSING-OVER IN VITRO IN HUMAN LYMPHOID CELLS.人类淋巴细胞体外交叉互换的细胞学证据。
Science. 1964 Apr 17;144(3616):298-301. doi: 10.1126/science.144.3616.298.
2
Mitotic crossing-over and segregation in man.人类中的有丝分裂交换与分离
Hum Genet. 1981;59(2):93-100. doi: 10.1007/BF00293053.
3
New views of the biochemistry of eucaryotic DNA replication revealed by aphidicolin, an unusual inhibitor of DNA polymerase alpha.通过一种不同寻常的DNA聚合酶α抑制剂——阿非科林揭示的真核生物DNA复制生物化学新观点。
Dokl Biochem Biophys. 2005 Nov-Dec;405:423-5. doi: 10.1007/s10628-005-0130-7.
4
Topoisomerase II hypersensitive sites in the 5'-terminal region of human dystrophin gene.
Dokl Biochem Biophys. 2001 May-Jun;378:198-200. doi: 10.1023/a:1011565229893.
5
Near-precise interchromosomal recombination and functional DNA topoisomerase II cleavage sites at MLL and AF-4 genomic breakpoints in treatment-related acute lymphoblastic leukemia with t(4;11) translocation.在伴有t(4;11)易位的治疗相关性急性淋巴细胞白血病中,MLL和AF-4基因组断点处近乎精确的染色体间重组及功能性DNA拓扑异构酶II切割位点
Proc Natl Acad Sci U S A. 2001 Aug 14;98(17):9802-7. doi: 10.1073/pnas.171309898. Epub 2001 Aug 7.
6
Inactivation of topoisomerase I or II may lead to recombination or to aberrant replication termination on both SV40 and yeast 2 micron DNA.拓扑异构酶I或II的失活可能导致SV40和酵母2微米DNA上的重组或异常复制终止。
Chromosoma. 1996 Oct;105(4):250-60. doi: 10.1007/BF02528774.
7
Integration of simian virus 40 into cellular DNA occurs at or near topoisomerase II cleavage hot spots induced by VM-26 (teniposide).猿猴病毒40整合进细胞DNA发生在由VM-26(替尼泊苷)诱导的拓扑异构酶II切割热点处或其附近。
Mol Cell Biol. 1993 Oct;13(10):6190-200. doi: 10.1128/mcb.13.10.6190-6200.1993.
8
High frequency of mutagen-induced chromatid exchanges at interstitial telomere-like DNA sequence blocks of Chinese hamster cells.中国仓鼠细胞间质性端粒样DNA序列块处诱变剂诱导的染色单体交换频率高。
Chromosome Res. 1995 Aug;3(5):281-4. doi: 10.1007/BF00713065.
9
Precise localization of the alpha-globin gene cluster within one of the 20- to 300-kilobase DNA fragments released by cleavage of chicken chromosomal DNA at topoisomerase II sites in vivo: evidence that the fragments are DNA loops or domains.在体内通过拓扑异构酶II位点切割鸡染色体DNA释放的20至300千碱基DNA片段之一内,α-珠蛋白基因簇的精确定位:片段为DNA环或结构域的证据。
Proc Natl Acad Sci U S A. 1991 Oct 1;88(19):8515-9. doi: 10.1073/pnas.88.19.8515.
10
Fusions near telomeres occur very early in the amplification of CAD genes in Syrian hamster cells.在叙利亚仓鼠细胞中,端粒附近的融合在CAD基因扩增的早期就会出现。
Proc Natl Acad Sci U S A. 1992 Jun 15;89(12):5427-31. doi: 10.1073/pnas.89.12.5427.
Cell. 1981 Mar;23(3):647-8. doi: 10.1016/0092-8674(81)90426-8.
4
DNA topoisomerase II mutant of Saccharomyces cerevisiae: topoisomerase II is required for segregation of daughter molecules at the termination of DNA replication.酿酒酵母的DNA拓扑异构酶II突变体:在DNA复制终止时,拓扑异构酶II对于子分子的分离是必需的。
Proc Natl Acad Sci U S A. 1984 May;81(9):2616-20. doi: 10.1073/pnas.81.9.2616.
5
Competitive inhibition of nicking--closing enzymes may explain some biological effects of DNA intercalators.
FEBS Lett. 1983 Aug 8;159(1-2):6-12. doi: 10.1016/0014-5793(83)80406-2.
6
Illegitimate recombination mediated in vitro by DNA gyrase of Escherichia coli: structure of recombinant DNA molecules.大肠杆菌DNA回旋酶体外介导的非法重组:重组DNA分子的结构
Proc Natl Acad Sci U S A. 1982 Jun;79(12):3724-8. doi: 10.1073/pnas.79.12.3724.
7
Effects of a new antitumor agent, epipodophyllotoxin, on growth and chromosomes in human hematopoietic cell lines.
Cancer Res. 1973 Dec;33(12):3123-9.
8
A manyfold increase in sister chromatid exchanges in Bloom's syndrome lymphocytes.布卢姆综合征淋巴细胞中姐妹染色单体交换的多重增加。
Proc Natl Acad Sci U S A. 1974 Nov;71(11):4508-12. doi: 10.1073/pnas.71.11.4508.
9
DNA replication and UV-induced DNA repair synthesis in human fibroblasts are much less sensitive than DNA polymerase alpha to inhibition by butylphenyl-deoxyguanosine triphosphate.在人类成纤维细胞中,DNA复制及紫外线诱导的DNA修复合成对丁基苯基脱氧鸟苷三磷酸抑制作用的敏感性远低于DNA聚合酶α。
Nucleic Acids Res. 1986 Sep 11;14(17):7093-102. doi: 10.1093/nar/14.17.7093.
10
DNA topoisomerase II is required for condensation and separation of mitotic chromosomes in S. pombe.DNA拓扑异构酶II是粟酒裂殖酵母有丝分裂染色体浓缩和分离所必需的。
Cell. 1987 Sep 11;50(6):917-25. doi: 10.1016/0092-8674(87)90518-6.