Vanhooff Virginie, Galloy Christine, Agaisse Hervé, Lereclus Didier, Révet Bernard, Hallet Bernard
Unité de Génétique, Institut des Sciences de la Vie, Université Catholique de Louvain, 5/6 Place Croix du Sud, B-1348 Louvain-la-Neuve, Belgium.
Mol Microbiol. 2006 May;60(3):617-29. doi: 10.1111/j.1365-2958.2006.05127.x.
Tn4430 is a distinctive transposon of the Tn3 family that encodes a tyrosine recombinase (TnpI) to resolve replicative transposition intermediates. The internal resolution site of Tn4430 (IRS, 116 bp) contains two inverted repeats (IR1 and IR2) at the crossover core site, and two additional TnpI binding motifs (DR1 and DR2) adjacent to the core. Deletion analysis demonstrated that DR1 and DR2 are not required for recombination in vivo and in vitro. Their function is to provide resolution selectivity to the reaction by stimulating recombination between directly oriented sites on a same DNA molecule. In the absence of DR1 and/or DR2, TnpI-mediated recombination of supercoiled DNA substrates gives a mixture of topologically variable products, while deletion between two wild-type IRSs exclusively produces two-noded catenanes. This demonstrates that TnpI binding to the accessory motifs DR1 and DR2 contributes to the formation of a specific synaptic complex in which catalytically inert recombinase subunits act as architectural elements to control recombination sites pairing and strand exchange. A model for the organization of TnpI/IRS recombination complex is presented.
Tn4430是Tn3家族中一种独特的转座子,它编码一种酪氨酸重组酶(TnpI)来解析复制性转座中间体。Tn4430的内部解离位点(IRS,116 bp)在交叉核心位点包含两个反向重复序列(IR1和IR2),以及与核心相邻的另外两个TnpI结合基序(DR1和DR2)。缺失分析表明,DR1和DR2在体内和体外重组中并非必需。它们的功能是通过刺激同一DNA分子上直接定向位点之间的重组,为反应提供解离选择性。在没有DR1和/或DR2的情况下,TnpI介导的超螺旋DNA底物重组会产生拓扑可变产物的混合物,而两个野生型IRS之间的缺失仅产生双节点连环体。这表明TnpI与辅助基序DR1和DR2的结合有助于形成特定的突触复合物,其中催化惰性的重组酶亚基作为结构元件来控制重组位点的配对和链交换。本文提出了TnpI/IRS重组复合物的组织模型。