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NBU1 IntN1 和 Orf2x 蛋白与附着位点 DNA 的相互作用。

Interactions of NBU1 IntN1 and Orf2x proteins with attachment site DNA.

机构信息

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

出版信息

J Bacteriol. 2013 Dec;195(24):5516-25. doi: 10.1128/JB.01011-13. Epub 2013 Oct 4.

Abstract

NBU1 is a mobilizable transposon found in Bacteroides spp. Mobilizable transposons require gene products from coresident conjugative transposons for excision and transfer to recipient cells. The integration of NBU1 requires IntN1, which has been identified as a tyrosine recombinase, as well as Bacteroides host factor BHFa. Excision of NBU1 is a more complicated process, involving five element-encoded proteins (IntN1, Orf2, Orf2x, Orf3, and PrmN1) as well as a Bacteroides host factor and a cis-acting DNA sequence. Little has been known about what role the proteins play in excision, although IntN1 and Orf2x have been shown to be the only proteins absolutely required for detectable excision. To determine where IntN1 and Orf2x bind during the excision of NBU1, both proteins were partially purified and tested in DNase I footprinting experiments with the excisive attachment sites attL and attR. The results demonstrate that IntN1 binds to four core-type sites that flank the region of cleavage and strand exchange, as well as six arm-type sites. A unique feature of the system is the location of DR2a and DR2b arm-type sites immediately downstream of the attL core. The DR1a, DR1b, DR3a, and DR3b arm-type sites were shown to be required for in vitro integration of NBU1. In addition, we have identified one Orf2x binding site (O1) on attL as well as a dA+dT-rich upstream element that is required for Orf2x interactions with O1.

摘要

NBU1 是一种可移动转座子,存在于拟杆菌属中。可移动转座子需要来自共存的接合转座子的基因产物才能进行切除和转移到受体细胞。NBU1 的整合需要 IntN1,它已被鉴定为酪氨酸重组酶,以及拟杆菌宿主因子 BHFa。NBU1 的切除是一个更复杂的过程,涉及五个元件编码的蛋白质(IntN1、Orf2、Orf2x、Orf3 和 PrmN1)以及拟杆菌宿主因子和一个顺式作用的 DNA 序列。虽然已经知道 IntN1 和 Orf2x 是可检测切除所必需的唯一蛋白质,但对这些蛋白质在切除中扮演的角色知之甚少。为了确定 IntN1 和 Orf2x 在 NBU1 切除过程中的结合位置,将这两种蛋白质部分纯化,并在 DNase I 足迹实验中使用切除附着位点 attL 和 attR 进行测试。结果表明,IntN1 结合到四个核心类型的位点,这些位点侧翼着切割和链交换区域,以及六个臂类型的位点。该系统的一个独特特征是 DR2a 和 DR2b 臂类型位点直接位于 attL 核心的下游。DR1a、DR1b、DR3a 和 DR3b 臂类型位点被证明是 NBU1 体外整合所必需的。此外,我们已经确定了 attL 上的一个 Orf2x 结合位点(O1)以及一个需要 Orf2x 与 O1 相互作用的富含 dA+dT 的上游元件。

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