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利用拓扑差异分析、单分子Förster 共振能量转移和单分子全内反射荧光显微镜技术分析 Flp 位点特异性重组过程中 DNA 伴侣的组织和链交换机制。

Organization of DNA partners and strand exchange mechanisms during Flp site-specific recombination analyzed by difference topology, single molecule FRET and single molecule TPM.

机构信息

Section of Molecular Genetics and Microbiology, Institute of Cell and Molecular Biology, University of Texas at Austin, Austin, TX 78712, USA.

Microscopy and Imaging Center, Department of Biology and Department of Biochemistry and Biophysics, Texas A&M University, College Station, TX 77843-2257, USA.

出版信息

J Mol Biol. 2014 Feb 20;426(4):793-815. doi: 10.1016/j.jmb.2013.11.017. Epub 2013 Nov 25.

Abstract

Flp site-specific recombination between two target sites (FRTs) harboring non-homology within the strand exchange region does not yield stable recombinant products. In negatively supercoiled plasmids containing head-to-tail sites, the reaction produces a series of knots with odd-numbered crossings. When the sites are in head-to-head orientation, the knot products contain even-numbered crossings. Both types of knots retain parental DNA configuration. By carrying out Flp recombination after first assembling the topologically well defined Tn3 resolvase synapse, it is possible to determine whether these knots arise by a processive or a dissociative mechanism. The nearly exclusive products from head-to-head and head-to-tail oriented "non-homologous" FRT partners are a 4-noded knot and a 5-noded knot, respectively. The corresponding products from a pair of native (homologous) FRT sites are a 3-noded knot and a 4-noded catenane, respectively. These results are consistent with non-homology-induced two rounds of dissociative recombination by Flp, the first to generate reciprocal recombinants containing non-complementary base pairs and the second to produce parental molecules with restored base pairing. Single molecule fluorescence resonance energy transfer (smFRET) analysis of geometrically restricted FRTs, together with single molecule tethered particle motion (smTPM) assays of unconstrained FRTs, suggests that the sites are preferentially synapsed in an anti-parallel fashion. This selectivity in synapse geometry occurs prior to the chemical steps of recombination, signifying early commitment to a productive reaction path. The cumulative topological, smFRET and smTPM results have implications for the relative orientation of DNA partners and the directionality of strand exchange during recombination mediated by tyrosine site-specific recombinases.

摘要

Flp 位点特异性重组两个靶位点(FRTs)之间的非同源性在链交换区域内不产生稳定的重组产物。在含有头对头位点的负超螺旋质粒中,反应产生一系列奇数交叉的结。当位点为头对头取向时,结产物包含偶数交叉。这两种类型的结保留亲本 DNA 构型。通过首先组装拓扑定义明确的 Tn3 resolvase 突触,然后进行 Flp 重组,可以确定这些结是通过连续还是解离机制产生的。来自头对头和头对头取向的“非同源”FRT 伙伴的几乎唯一产物是 4 节点结和 5 节点结,分别。来自一对天然(同源)FRT 位点的相应产物分别是 3 节点结和 4 节点连环结。这些结果与 Flp 诱导的两轮非同源性解离重组一致,第一轮产生含有非互补碱基对的互易重组体,第二轮产生恢复碱基配对的亲本分子。受几何限制的 FRT 的单分子荧光共振能量转移(smFRET)分析,以及不受限制的 FRT 的单分子系绳粒子运动(smTPM)测定,表明这些位点优先以反平行方式形成突触。这种在突触几何形状上的选择性发生在重组的化学步骤之前,标志着对有生产力的反应途径的早期承诺。累积的拓扑、smFRET 和 smTPM 结果对酪氨酸位点特异性重组酶介导的重组过程中 DNA 伙伴的相对取向和链交换的方向性具有重要意义。

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