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Precise Excision of IS5 from the Intergenic Region between the fucPIK and the fucAO Operons and Mutational Control of fucPIK Operon Expression in Escherichia coli ▿

机译:从fucPIK和fucAO操纵子之间的基因间区域精确切除IS5,并控制fucPIK操纵子在大肠杆菌中的表达突变▿

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摘要

Excision of transposable genetic elements from host DNA occurs at low frequencies and is usually imprecise. A common insertion sequence element in Escherichia coli, IS5, has been shown to provide various benefits to its host by inserting into specific sites. Precise excision of this element had not previously been demonstrated. Using a unique system, the fucose (fuc) regulon, in which IS5 insertion and excision result in two distinct selectable phenotypes, we have demonstrated that IS5 can precisely excise from its insertion site, restoring the wild-type phenotype. In addition to precise excision, several “suppressor” insertion, deletion, and point mutations restore the wild-type Fuc+ phenotype to various degrees without IS5 excision. The possible bases for these observations are discussed.
机译:从宿主DNA中切除可转座遗传元件的频率很低,通常不精确。大肠杆菌中常见的插入序列元件IS5通过插入特定位点可为其宿主提供多种益处。以前没有证明过该元素的精确切除。使用独特的系统,岩藻糖(fuc)调节剂,其中IS5插入和切除导致两个不同的可选表型,我们证明了IS5可以从其插入位点精确切除,从而恢复了野生型表型。除精确切除外,无需IS5切除,多个“抑制子”的插入,缺失和点突变可将野生型Fuc +表型恢复到不同程度。讨论了这些观察的可能依据。

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