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在来自玉米黑粉菌野生型和top1-菌株的无细胞提取物中核小体DNA的组装。

Assembly of nucleosomal DNA in a cell-free extract from wild-type and top1- strains of Ustilago maydis.

作者信息

Dutta S, Gerhold D, Kmiec E B

机构信息

Department of Pharmacology, Jefferson Cancer Institute, Thomas Jefferson University, Philadelphia, PA 19107, USA.

出版信息

Mol Gen Genet. 1995 Oct 25;248(6):675-85. doi: 10.1007/BF02191707.

Abstract

An in vitro nucleosome assembly system has been established from cell-free extracts of the fungus Ustilago maydis. The extract catalyzed DNA supercoiling in the absence of exogenously added co-factors such as ATP and MgCl2 and was inhibited by moderate concentrations (200 mM) of KCl or NaCl. DNA supercoiling occurs via the formation of nucleosomes. Similar extracts, displaying the same activity, were prepared from Saccharomyces cerevisiae and Candida albicans, suggesting that the extract preparation protocol may be useful for many lower eukaryotic systems. An extract prepared from a strain of U. maydis lacking topoisomerase I failed to catalyze nucleosome assembly, clearly implicating this enzyme in this process. Addition of purified topoisomerase I, and, to a lesser extent, topoisomerase II, to the top1- extract regenerated the supercoiling activity. Our results provide a method for preparing assembly extracts from organisms, that are particularly amenable to genetic manipulation.

摘要

已从真菌玉米黑粉菌的无细胞提取物中建立了一种体外核小体组装系统。该提取物在没有外源添加诸如ATP和MgCl2等辅助因子的情况下催化DNA超螺旋化,并且受到中等浓度(200 mM)的KCl或NaCl的抑制。DNA超螺旋化通过核小体的形成而发生。从酿酒酵母和白色念珠菌制备了具有相同活性的类似提取物,这表明提取物制备方案可能对许多低等真核生物系统有用。从缺乏拓扑异构酶I的玉米黑粉菌菌株制备的提取物未能催化核小体组装,这清楚地表明该酶参与了这一过程。向top1 - 提取物中添加纯化的拓扑异构酶I以及在较小程度上添加拓扑异构酶II可恢复超螺旋化活性。我们的结果提供了一种从特别适合基因操作的生物体中制备组装提取物的方法。

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