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交叉点与拓扑异构酶I切割位点的关联:一种非同源重组模型

Association of crossover points with topoisomerase I cleavage sites: a model for nonhomologous recombination.

作者信息

Bullock P, Champoux J J, Botchan M

出版信息

Science. 1985 Nov 22;230(4728):954-8. doi: 10.1126/science.2997924.

Abstract

Nonhomologous DNA recombination is frequently observed in somatic cells upon the introduction of DNA into cells or in chromosomal events involving sequences already stably carried by the genome. In this report, the DNA sequences at the crossover points for excision of SV40 from chromosomes were shown to be associated with eukaryotic topoisomerase I cleavage sites in vitro. The precise location of the cleavage sites relative to the crossover points has suggested a general model for nonhomologous recombination mediated by topoisomerase I.

摘要

当将DNA导入细胞时,在体细胞中或在涉及基因组已稳定携带的序列的染色体事件中,经常观察到非同源DNA重组。在本报告中,从染色体上切除SV40的交叉点处的DNA序列在体外显示与真核拓扑异构酶I切割位点相关。切割位点相对于交叉点的精确位置提示了拓扑异构酶I介导的非同源重组的一般模型。

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