首页> 美国卫生研究院文献>Nucleic Acids Research >Site-specific recombination by the beta protein from the streptococcal plasmid pSM19035: minimal recombination sequences and crossing over site.
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Site-specific recombination by the beta protein from the streptococcal plasmid pSM19035: minimal recombination sequences and crossing over site.

机译:来自链球菌质粒pSM19035的β蛋白的位点特异性重组:最小的重组序列和跨位点。

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摘要

The beta recombinase from the broad host range Grampositive plasmid pSM19035 catalyzes intramolecular site-specific recombination between two directly or inversely oriented recombination sites in the presence of a chromatin-associated protein (Hbsu). The recombination site had been localized to a 447 bp DNA segment from pSM19035. This segment includes a 90 bp region that contains two adjacent binding sites (I and II) for beta protein dimers. Using in vitro recombination assays, we show that this 90 bp region is necessary and sufficient for beta protein-mediated recombination; this defines the six site as the region required for beta protein binding. The point of crossing over has been localized to the center of site I. Hbsu has a strong binding affinity for an unknown site located within the 447 bp segment containing the six site. We discuss the possibility that Hbsu recognizes an altered DNA structure, rather than a specific sequence, generated in the synaptic complex.
机译:来自广泛宿主范围的革兰氏阳性质粒pSM19035的β重组酶在存在染色质相关蛋白(Hbsu)的情况下催化两个直接或反向定向重组位点之间的分子内位点特异性重组。重组位点已定位于来自pSM19035的447 bp DNA片段。该区段包括一个90 bp的区域,其中包含两个相邻的β蛋白二聚体结合位点(I和II)。使用体外重组测定法,我们表明,这个90 bp的区域对于β蛋白介导的重组是必要和充分的;这将六个位点定义为β蛋白结合所需的区域。交叉点已定位在位点I的中心。Hbsu对位于包含六个位点的447 bp片段内的未知位点具有很强的结合亲和力。我们讨论了Hbsu识别突触复合物中生成的DNA结构改变而不是特定序列的可能性。

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