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酪氨酸重组酶IntDOT对错配重叠霍利迪连接中间体的拆分

Resolution of Mismatched Overlap Holliday Junction Intermediates by the Tyrosine Recombinase IntDOT.

作者信息

Ringwald Kenneth, Yoneji Sumiko, Gardner Jeffrey

机构信息

Department of Microbiology, University of Illinois Urbana-Champaign, Urbana, Illinois, USA

Department of Microbiology, University of Illinois Urbana-Champaign, Urbana, Illinois, USA.

出版信息

J Bacteriol. 2017 Apr 25;199(10). doi: 10.1128/JB.00873-16. Print 2017 May 15.

Abstract

CTnDOT is an integrated conjugative element found in species. CTnDOT contains and transfers antibiotic resistance genes. The element integrates into and excises from the host chromosome via a Holliday junction (HJ) intermediate as part of a site-specific recombination mechanism. The CTnDOT integrase, IntDOT, is a tyrosine recombinase with core-binding, catalytic, and amino-terminal (N) domains. Unlike well-studied tyrosine recombinases, such as lambda integrase (Int), IntDOT is able to resolve Holliday junctions containing heterology (mismatched bases) between the sites of strand exchange. All known natural isolates of CTnDOT contain mismatches in the overlap region between the sites of strand exchange. Previous work showed that IntDOT was unable to resolve synthetic Holliday junctions containing mismatched bases to products in the absence of the arm-type sites and a DNA-bending protein. We constructed synthetic HJs with the arm-type sites and tested them with the host factor (BHFa). We found that the addition of BHFa stimulated resolution of HJ intermediates with mismatched overlap regions to products. In addition, the L1 site is required for directionality of the reaction, particularly when the HJ contains mismatches. BHFa is required for product formation when the overlap region contains mismatches, and it stimulates resolution to products when the overlap region is identical. Without this DNA bending, the N domain of IntDOT is likely unable to bind the L1 arm-type site. These findings suggest that BHFa bends DNA into the necessary conformation for the higher-order complexes, including the L1 site, that are required for product formation. CTnDOT is a mobile element that carries antibiotic resistance genes and moves by site-selective recombination and subsequent conjugation. The recombination reaction is catalyzed by an integrase IntDOT that is a member of the tyrosine recombinase family. The reaction proceeds through ordered strand exchanges that generate a Holliday junction (HJ) intermediate. Unlike other tyrosine recombinases, IntDOT can resolve HJs containing mismatched bases in the overlap region , as is the case under natural conditions. However, HJ intermediates including only IntDOT core-type sites cannot be resolved to products if the HJ intermediate contains mismatched bases. We added arm-type sites in and in to the HJ intermediates and the protein BHFa to study the requirements for higher-order nucleoprotein complexes.

摘要

CTnDOT是在多种物种中发现的一种整合型接合元件。CTnDOT携带并转移抗生素抗性基因。该元件通过霍利迪连接体(HJ)中间体整合到宿主染色体并从宿主染色体上切除,这是位点特异性重组机制的一部分。CTnDOT整合酶IntDOT是一种具有核心结合结构域、催化结构域和氨基末端(N)结构域的酪氨酸重组酶。与经过充分研究的酪氨酸重组酶(如λ整合酶(Int))不同,IntDOT能够解析在链交换位点之间包含异源(错配碱基)的霍利迪连接体。所有已知的CTnDOT天然分离株在链交换位点之间的重叠区域都含有错配。先前的研究表明,在没有臂型位点和一种DNA弯曲蛋白的情况下,IntDOT无法将含有错配碱基的合成霍利迪连接体解析为产物。我们构建了带有臂型位点的合成HJs,并与宿主因子(BHFa)一起对其进行测试。我们发现添加BHFa可促进具有错配重叠区域的HJ中间体解析为产物。此外,L1位点对于反应的方向性是必需的,特别是当HJ包含错配时。当重叠区域包含错配时,产物形成需要BHFa,并且当重叠区域相同时,它会促进解析为产物。没有这种DNA弯曲,IntDOT的N结构域可能无法结合L1臂型位点。这些发现表明,BHFa将DNA弯曲成产物形成所需的高阶复合物(包括L1位点)的必要构象。CTnDOT是一种携带抗生素抗性基因的可移动元件,通过位点选择性重组和随后的接合进行移动。重组反应由属于酪氨酸重组酶家族的整合酶IntDOT催化。反应通过有序的链交换进行,产生霍利迪连接体(HJ)中间体。与其他酪氨酸重组酶不同,IntDOT可以解析在重叠区域包含错配碱基的HJs,天然条件下就是这种情况。然而,如果HJ中间体包含错配碱基,仅包含IntDOT核心型位点的HJ中间体无法解析为产物。我们在HJ中间体中添加了臂型位点,并添加了蛋白质BHFa,以研究高阶核蛋白复合物的需求。

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本文引用的文献

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