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II型DNA拓扑异构酶特异性抑制剂VM26对体外SV40染色质复制的影响。

Effects of VM26, a specific inhibitor of type II DNA topoisomerase, on SV40 chromatin replication in vitro.

作者信息

Richter A, Strausfeld U

机构信息

Universität Konstanz, Fakultät Für Biologie, FRG.

出版信息

Nucleic Acids Res. 1988 Nov 11;16(21):10119-29. doi: 10.1093/nar/16.21.10119.

Abstract

We have examined the influence of VM26 (teniposide), a specific inhibitor of mammalian type II DNA topoisomerase, on the replication of SV40 minichromosomes in vitro. The replication system we used consists of replicative intermediate SV40 chromatin as substrate which is converted to mature SV40 chromatin in the presence of ATP, deoxynucleotides and a protein extract from uninfected cells. The addition of 100 microM VM26 to this system reduces DNA synthesis to 70 to 80 percent of the control and leads to an accumulation of 'late replicative intermediates'. The VM26 induced block of replication was not released by the addition of large quantities of type I DNA topoisomerase. We conclude, that type II DNA topoisomerase is essential for the final replication steps leading from late Cairns structures of replicative intermediates to monomeric minichromosomes. It appears that type I DNA topoisomerase can function as a swivelase during most of the replicative elongation phase, but must later be replaced by type II DNA topoisomerase.

摘要

我们研究了哺乳动物II型DNA拓扑异构酶的特异性抑制剂VM26(替尼泊苷)对SV40微型染色体体外复制的影响。我们使用的复制系统以复制中间体SV40染色质为底物,在ATP、脱氧核苷酸和未感染细胞的蛋白质提取物存在的情况下,该底物会转化为成熟的SV40染色质。向该系统中添加100微摩尔的VM26会使DNA合成降至对照的70%至80%,并导致“晚期复制中间体”的积累。添加大量的I型DNA拓扑异构酶并不能解除VM26诱导的复制阻滞。我们得出结论,II型DNA拓扑异构酶对于从复制中间体的晚期凯恩斯结构到单体微型染色体的最终复制步骤至关重要。似乎I型DNA拓扑异构酶在大多数复制延伸阶段都可以作为旋转酶发挥作用,但后期必须被II型DNA拓扑异构酶取代。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f6b5/338841/d477a186f5fb/nar00163-0243-a.jpg

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