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转录调控了喹酸诱导的大肠杆菌染色体上特定位点的DNA回旋酶切割。

Transcription regulates oxolinic acid-induced DNA gyrase cleavage at specific sites on the E. coli chromosome.

作者信息

Condemine G, Smith C L

机构信息

Laboratoire de Microbiologie, INSA Bat 406, Villeurbanne, France.

出版信息

Nucleic Acids Res. 1990 Dec 25;18(24):7389-96. doi: 10.1093/nar/18.24.7389.

Abstract

Prominent DNA gyrase-mediated cleavage sites, induced by oxolinic acid, occur at specific, but infrequent, locations on the Escherichia coli chromosome. These sites, which we call toposites, may represent high affinity DNA gyrase binding sites or may mark chromosomal regions that accumulate superhelical stress. Toposites are usually grouped in 5 to 10 kb clusters that are mostly 50 to 100 kb apart. The total number of clusters on the chromosome is between 50 and 100. The location of sites depends on the local sequence. The extent of DNA gyrase cleavage at toposites can be strongly modulated by transcription occurring at as far as 35 kb away.

摘要

由恶喹酸诱导产生的显著的DNA促旋酶介导的切割位点,出现在大肠杆菌染色体上特定但不常见的位置。这些位点,我们称之为拓扑位点,可能代表高亲和力的DNA促旋酶结合位点,或者可能标记积累超螺旋应力的染色体区域。拓扑位点通常成簇分布,每簇5到10 kb,大多相距50到100 kb。染色体上簇的总数在50到100之间。位点的位置取决于局部序列。在距离拓扑位点达35 kb处发生的转录可强烈调节拓扑位点处DNA促旋酶的切割程度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ceef/332877/f5ed58b9030f/nar00208-0179-a.jpg

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