Trieu-Cuot P, Poyart-Salmeron C, Carlier C, Courvalin P
Unité des Agents Antibactériens, Institut Pasteur, Paris, France.
Mol Microbiol. 1993 Apr;8(1):179-85. doi: 10.1111/j.1365-2958.1993.tb01214.x.
Excision and integration of Tn1545 occur by reciprocal site-specific recombination between 6 (or 7) bp variable sequences present in the recombining attachment (att) sites and designated overlap regions. We devised an assay for Tn1545 transposition in which derivatives containing the cis-acting transposition sequences (attTn 1545) integrate into a target replicon when complemented in trans by the transposon-encoded integrase Int-Tn. This assay was used to determine the characteristics of the DNA sequence that influence target site selection. Characterization of several integration sites indicated that a 20 bp segment, designated attB, contains the sequences required for target activity. It also appeared that (i) the target activity depends upon the extent of homology between the 7bp segments flanking the overlap regions in attB and attTn 1545, and (ii) the degree of homology between the two recombining overlap regions does not affect the level of target activity and has no influence on integration orientation.
Tn1545的切除和整合通过重组附着(att)位点中存在的6(或7)个碱基对可变序列与指定的重叠区域之间的特异性位点重组发生。我们设计了一种Tn1545转座测定法,其中含有顺式作用转座序列(attTn 1545)的衍生物在由转座子编码的整合酶Int-Tn反式互补时整合到目标复制子中。该测定法用于确定影响靶位点选择的DNA序列的特征。几个整合位点的表征表明,一个20个碱基对的片段,称为attB,包含靶活性所需的序列。还发现:(i)靶活性取决于attB和attTn 1545中重叠区域侧翼的7个碱基对片段之间的同源程度,并且(ii)两个重组重叠区域之间的同源程度不影响靶活性水平,并且对整合方向没有影响。