Permana P A, Ferrer C A, Snapka R M
Department of Radiology, Ohio State University, Columbus 43210.
Biochem Biophys Res Commun. 1994 Jun 30;201(3):1510-7. doi: 10.1006/bbrc.1994.1875.
High resolution gel electrophoresis was used to demonstrate an inverse relationship between catenation linking number and superhelicity in highly catenated simian virus 40 chromosomes caused by exposure to the topoisomerase II inhibitor ICRF-193. Since ICRF-193 does not unwind DNA, we conclude that the decreased superhelicity in catenated SV40 daughter chromosomes is a direct result of increased catenation. It is likely that catenation decreases superhelicity by interfering with the formation of nucleosomes. The absence of normal chromatin structure in regions of catenation may facilitate access to topoisomerase II under normal conditions. ICRF-193 does not prevent initiation of SV40 DNA replication.
高分辨率凝胶电泳用于证明在暴露于拓扑异构酶II抑制剂ICRF-193后,高度连环化的猿猴病毒40染色体中连环连接数与超螺旋度之间的反比关系。由于ICRF-193不会使DNA解旋,我们得出结论,连环化的SV40子代染色体中超螺旋度的降低是连环化增加的直接结果。连环化可能通过干扰核小体的形成来降低超螺旋度。在连环化区域缺乏正常的染色质结构可能在正常条件下便于拓扑异构酶II的作用。ICRF-193不会阻止SV40 DNA复制的起始。