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利用具有不同内源性拓扑异构酶II水平的体细胞提取物和细胞核在体外进行有丝分裂染色质凝聚。

Mitotic chromatin condensation in vitro using somatic cell extracts and nuclei with variable levels of endogenous topoisomerase II.

作者信息

Wood E R, Earnshaw W C

机构信息

Department of Cell Biology and Anatomy, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.

出版信息

J Cell Biol. 1990 Dec;111(6 Pt 2):2839-50. doi: 10.1083/jcb.111.6.2839.

Abstract

We report the development of a new method for producing mitotic extracts from tissue culture cells. These extracts reproducibly promote the condensation of chromatin in vitro when incubated with purified interphase nuclei. This condensation reaction is not species specific, since nuclei from chicken, human, and hamster cell lines all undergo chromatin condensation upon incubation with the extract. We have used this extract to investigate the role of DNA topoisomerase II (topo II) in the chromosome condensation process. Chromatin condensation does not require the presence of soluble topo II in the mitotic extract. However, the extent of formation of discrete chromosome-like structures correlates with the level of endogenous topo II present in the interphase nuclei. Our results further suggest that chromatin condensation in this extract may involve two processes: chromatin compaction and resolution into discrete chromosomes.

摘要

我们报告了一种从组织培养细胞中制备有丝分裂提取物的新方法。当与纯化的间期细胞核一起孵育时,这些提取物在体外可重复性地促进染色质凝聚。这种凝聚反应不是物种特异性的,因为来自鸡、人类和仓鼠细胞系的细胞核在与提取物孵育时都会发生染色质凝聚。我们使用这种提取物来研究DNA拓扑异构酶II(拓扑II)在染色体凝聚过程中的作用。有丝分裂提取物中可溶性拓扑II的存在不是染色质凝聚所必需的。然而,离散的染色体样结构的形成程度与间期细胞核中内源性拓扑II的水平相关。我们的结果进一步表明,这种提取物中的染色质凝聚可能涉及两个过程:染色质压缩和解析为离散的染色体。

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