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拓扑异构酶I的基因失活抑制了大肠杆菌染色体复制起始中的缺陷。

Genetic inactivation of topoisomerase I suppresses a defect in initiation of chromosome replication in Escherichia coli.

作者信息

Louarn J, Bouché J P, Patte J, Louarn J M

出版信息

Mol Gen Genet. 1984;195(1-2):170-4. doi: 10.1007/BF00332741.

Abstract

A strain of Escherichia coli K12 harboring simultaneously the temperature-sensitive dnaA46 mutation and a deletion of the trp-topA-cysB region plates with the same full efficiency at 30 degrees C and 42 degrees C. We have analyzed the possible involvement of the gene coding for topoisomerase I, topA, in this suppression phenomenon. The Ts phenotype was retrieved upon introduction of a plasmid-borne DNA fragment including an active topA gene into this strain, but not upon introduction of the same fragment harboring a topA::Tn1000 insertion. Replication seems to remain DnaA-dependent in the delta (topA) strain, however, since we have been unable to introduce a dnaA::Tn10 allele. We propose either that the dnaA46 gene product is overproduced and compensates for its thermal inactivation, or that initiation at oriC demands less DnaA protein in the absence of topoisomerase I.

摘要

一株同时携带温度敏感型 dnaA46 突变和 trp-topA-cysB 区域缺失的大肠杆菌 K12 在 30℃和 42℃时具有相同的完全平板效率。我们分析了编码拓扑异构酶 I 的基因 topA 可能参与这种抑制现象的情况。当将包含活性 topA 基因的质粒携带的 DNA 片段导入该菌株时,Ts 表型得以恢复,但导入携带 topA::Tn1000 插入的相同片段时则不然。然而,在 delta(topA)菌株中,复制似乎仍然依赖于 DnaA,因为我们无法导入 dnaA::Tn10 等位基因。我们提出,要么 dnaA46 基因产物过量产生并补偿其热失活,要么在没有拓扑异构酶 I 的情况下,oriC 处的起始需要较少的 DnaA 蛋白。

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