Charron M, Hancock R
Centre de Recherche en Cancérologie, l'Université Laval, Hôtel-Dieu Hospital, Québec, Canada.
Biochemistry. 1990 Oct 16;29(41):9531-7. doi: 10.1021/bi00493a006.
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)
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)