High yield of endoreduplication induced by ICRF-193:: a topoisomerase II catalytic inhibitor

被引:17
|
作者
Pastor, N [1 ]
Flores, MJ [1 ]
Domínguez, I [1 ]
Mateos, S [1 ]
Cortés, F [1 ]
机构
[1] Univ Seville, Fac Biol, Dept Cell Biol, E-41012 Seville, Spain
关键词
endoreduplication; diplochromosomes; topoisomerase II; ICRF-193; EM9;
D O I
10.1016/S1383-5718(02)00029-3
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
An uncommonly high yield of spontaneous endoreduplication is a feature of the CHO mutant EM9, besides its defective repair of single, as well as double-DNA strand-breaks and its extraordinarily elevated yield of sister chromatid exchanges (SCEs) after bromodeoxyuridine (BrdU) incorporation into DNA. Since the nuclear enzyme topoisomerase II (topo II) has been reported to be responsible for the segregation of daughter chromosomes during mitosis, in the present investigation we have made use of the bisdioxopiperazine ICRF-193, a topo II catalytic inhibitor that interferes with the normal turnover of the enzyme. In order to see whether both EM9 cells and its parental cell line AA8, which show differences in the spontaneous frequency of endoreduplicated cells are or not equally sensitive to the topo II catalytic inhibitor, both cell lines have been treated with a range of doses of the bisdioxopiperazine. Our results show that both cell lines respond to the treatment entering in an endoreduplication cycle, but the EM9 cells are extremely sensitive to the inhibition of topo II. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:113 / 120
页数:8
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